key: cord-0071294-o55586pi
authors: Shapiro, Daniel D.; Soeung, Melinda; Perelli, Luigi; Dondossola, Eleonora; Surasi, Devaki Shilpa; Tripathi, Durga N.; Bertocchio, Jean-Philippe; Carbone, Federica; Starbuck, Michael W.; Van Alstine, Michael L.; Rao, Priya; Katz, Matthew H. G.; Parker, Nathan H.; Shah, Amishi Y.; Carugo, Alessandro; Heffernan, Timothy P.; Schadler, Keri L.; Logothetis, Christopher; Walker, Cheryl L.; Wood, Christopher G.; Karam, Jose A.; Draetta, Giulio F.; Tannir, Nizar M.; Genovese, Giannicola; Msaouel, Pavlos
title: Association of High-Intensity Exercise with Renal Medullary Carcinoma in Individuals with Sickle Cell Trait: Clinical Observations and Experimental Animal Studies
date: 2021-11-30
journal: Cancers (Basel)
DOI: 10.3390/cancers13236022
sha: 1cd91e113a9ced8554bf959f7a785d31b249c762
doc_id: 71294
cord_uid: o55586pi

SIMPLE SUMMARY: Renal medullary carcinoma (RMC) is a rare but highly aggressive malignancy that affects individuals of African descent with sickle cell trait (SCT). The driver of RMC pathogenesis is thought to be renal medullary ischemia from red blood cell sickling in the setting of SCT. Currently, no modifiable risk factors for RMC have been identified that explain why certain individuals with SCT develop RMC. Prior studies have demonstrated that high-intensity exercise increases adverse events related to red blood cell sickling. We hypothesized that high-intensity exercise may increase the risk of RMC. We used multiple sources of evidence including retrospective and prospective review of RMC patient exercise activity, objective measurements of skeletal muscle surface area, and measurement of hypoxia levels in the renal medulla of mice with SCT following high or moderate-intensity exercise. Our results suggest that high but not moderate-intensity exercise may be associated with the development of RMC among individuals with SCT. ABSTRACT: Renal medullary carcinoma (RMC) is a lethal malignancy affecting individuals with sickle hemoglobinopathies. Currently, no modifiable risk factors are known. We aimed to determine whether high-intensity exercise is a risk factor for RMC in individuals with sickle cell trait (SCT). We used multiple approaches to triangulate our conclusion. First, a case-control study was conducted at a single tertiary-care facility. Consecutive patients with RMC were compared to matched controls with similarly advanced genitourinary malignancies in a 1:2 ratio and compared on rates of physical activity and anthropometric measures, including skeletal muscle surface area. Next, we compared the rate of military service among our RMC patients to a similarly aged population of black individuals with SCT in the U.S. Further, we used genetically engineered mouse models of SCT to study the impact of exercise on renal medullary hypoxia. Compared with matched controls, patients with RMC reported higher physical activity and had higher skeletal muscle surface area. A higher proportion of patients with RMC reported military service than expected compared to the similarly-aged population of black individuals with SCT. When exposed to high-intensity exercise, mice with SCT demonstrated significantly higher renal medulla hypoxia compared to wild-type controls. These data suggest high-intensity exercise is the first modifiable risk factor for RMC in individuals with SCT.

Renal medullary carcinoma (RMC) is a lethal kidney malignancy that almost exclusively afflicts young individuals of African descent with sickle hemoglobinopathies, predominantly sickle cell trait (SCT), and is associated with red blood cell (RBC) sickling in the renal medulla [1] [2] [3] . RMC accounts for <0.5% of all renal cell carcinomas, and the median age at diagnosis is 28 years old [3] . Males are predominantly affected over females in a 3:1 ratio. All cases of RMC are characterized by loss of SMARCB1 expression, which is a component of the SWI/SNF chromatin remodeling complex [3] . Sickle cell trait, which is the predominant sickle hemoglobinopathy affecting patients with RMC in more than 85% of cases, is the most common sickle hemoglobinopathy with a population genotype rate 55 times more prevalent than sickle cell disease [2, 3] . Sickle cells are commonly found in the renal medulla of individuals with SCT, despite the absence of RBC sickling in the peripheral blood [2, 3] . Sickle cell trait is found in approximately 300 million individuals worldwide [4] , and between 1/20,000 to 1/39,000 will develop RMC [5] . RMC is resistant to traditional targeted therapies used in other renal cell carcinomas (RCCs), and patients have few therapeutic options. More than 90% of patients will be diagnosed with advanced (stage III or IV) RMC, and the prognosis is poor with a median survival of only 13 months from diagnosis [2, 6, 7] . There is a critical need to develop new ways to screen, diagnose, and prevent RMC, informed by a better understanding of what drives its unique epidemiology.

It is unclear why only some individuals with sickle hemoglobinopathies develop RMC. All reported cases are sporadic without familial clustering or identifiable genetic risk factors other than the presence of a sickle hemoglobinopathy. Previous reports hypothesized tissue hypoxia caused by RBC sickling in the renal medulla results in RMC pathogenesis [1, 3, 8] . The longer length of the right renal artery can worsen hypoxia in the right medulla compared to the left, and this difference may explain the predilection of RMC for the right kidney [3] . High-intensity exercise has been associated with an increased risk of exertional rhabdomyolysis and sudden cardiac death in individuals with SCT, presumably due to tissue hypoxia from RBC sickling [9, 10] . To date, however, the renal sequela of exercise in the setting of SCT have not been investigated, and most studies addressing RMC have not addressed risk factors beyond the presence of SCT [2, 5] . We utilized our uniquely large dataset of patients with RMC and animal models of SCT with the primary objective of determining whether high-intensity exercise is a risk factor for RMC. 

From January 2011 to February 2020, we collected clinical and demographic data from patients with pathologically confirmed RMC treated at a single institution. All histology was reviewed by a genitourinary pathology expert with over 15 years of experience, and RMC samples were confirmed to be SMARCB1 negative by immunohistochemistry. To determine the presence of high-intensity physical activity, both RMC and control patient medical records were retrospectively evaluated by two observers to reach consensus. We applied the same strategy to all patients based on the American Heart Association's "Guide to Physical Activity Assessment" [11] . We first evaluated the four dimensions of physical activity, including the mode or type of activity (e.g., walking, cycling, weightlifting), frequency of performing the activity, duration of performing the activity, and the intensity of performing the activity. In addition, we evaluated the domains of physical activity, including occupational, domestic, transportation, and leisure time. Based on reported occupations among our RMC and control patients, we only considered occupations with significant manual labor or high-intensity exercise component as indicative of significant physical activity. These occupations included construction, professional/full time athlete, and personal exercise trainers. Domestic physical activity such as housework, yard work, or childcare were not considered indicative of significant high-intensity physical activity. Patient reported exercise including participation in sporting events, bicycling, weightlifting, running, and martial arts ≥3 times per week were considered significant physical activity. The number of hours patients participated in each physical activity per week were collected; however, this was infrequently reported among patients both in the RMC and control cohorts. These criteria were applied equally to both groups. A binary physical activity index was then created to compare the RMC and matched controls. If a patient reported at least one domain of physical activity, they were tabulated as 1 or "yes" and if no physical activity domains were reported then they were tabulated as 0 or "no". This binary system would reduce bias when comparing the proportion of physical activity between the two cohorts.

We generated a matched control group evaluated in the same department and time period to determine whether reported exercise (as measured by the activity index) and anthropometric measurements were associated with RMC using a case-control approach. Because advanced malignancies can lead to sarcopenia and cachexia [12] , we ensured that control patients had similarly staged genitourinary malignancies and were each matched with an RMC patient in a 2:1 ratio based on age and biologic sex as able.

We objectively measured the cross-sectional area of skeletal muscle (SM) and subcutaneous adipose (SA) compartments using computed tomography (CT) imaging studies. Images were obtained and analyzed at the initial diagnosis of cancer prior to initiation of systemic therapy to avoid the changes induced by systemic therapy on either SM or SA. The SM and SA areas were measured using axial images at the midpoint of the L3 vertebral body as previously described [13] . Cross-sectional areas were standardized to the square of height in meters for each patient. Analysis was performed using SliceOMatic v5.0 (TomoVision, Magog, QC, Canada).

We hypothesized that active-duty military service may increase the rate of highintensity exercise and be more prevalent in our RMC cohort. We accordingly compared the proportion of military service among our RMC cohort to that of a similarly aged (age 20-40 years old) U.S. population of black individuals with SCT [5, 14, 15] . Details on the population estimate can be found in the Supplementary Methods. 

After evaluating our retrospective findings, we began prospectively gathering detailed information on the exercise activity of patients with RMC seen as new patients at our institution (N = 7) from March 2020 to January 2021. Patients graded their exercise intensity as high, moderate, or none. High-intensity exercise was defined as achieving ≥80% maximal heart rate during each exercise session [16] . Moderate-intensity exercise was defined as exercise performed in a continuous manner at lower intensities than highintensity exercise during each exercise session [16] . Patients also reported how much time per week was spent exercising. Lastly, we recorded the type of exercise activity and how long patients had been involved in these activities prior to the diagnosis of RMC.

Details on the generation of genetically engineered mouse models (GEMMs) of SCT and appropriate wild-type controls are provided in the Supplementary Methods. For exercise experiments, adult untrained wild-type (N = 11) and SCT (N = 10) mice were placed on a six-lane mechanical treadmill (Columbus Instruments) that was quickly brought up to 12-15 m/min to model acute exercise. Each session lasted 10 min. For in vivo imaging system (IVIS) studies, mice were imaged prior to exercise, immediately after exercise, and one hour after exercise. Information regarding the use of IVIS can be found in Supplementary Methods. Two different intensities were used to measure the effect of increasing exercise intensity on renal hypoxia. As previously established [17] , moderateintensity exercise was defined as 12 m/min, which correlates with 65% to 75% VO 2 max, i.e., a brisk walk. High-intensity exercise was defined as 15 m/min, which correlates with approximately ≥80% VO 2 max [17] .

To reduce bias from inappropriate regression adjustment for colliders or mediators rather than confounders, we generated structural causal models (SCMs) to codify our pre-specified model that guided statistical analyses evaluating the relationship between reported exercise history, anthropometric measurements, and the diagnosis of RMC [18] [19] [20] . Multivariable unconditional and conditional logistic regression models were used to determine the association between reported exercise history or anthropometric measures with RMC diagnosis (compared with diagnosis of the matched control genitourinary malignancies) following adjustment for confounders (age, biologic sex, and race) identified by the SCMs (Supplementary Figure S1) . In order to determine if there was an unmeasured confounder that could "explain away" the observed association between our exposure of interest (i.e., activity index) and outcome (i.e., RMC diagnosis), we performed a robust sensitivity analysis, as described by Cinelli and Hazlett, that does not require any assumptions on the functional form of the observed association or on the distribution and number of unobserved confounders [21] . To perform this analysis, we used the package sensemakr for STATA. We first calculated the robustness value (RV), which provides a reference point to assess the robustness of the regression coefficient of the activity index to unobserved confounding. If a confounder's association to the exposure and to the outcome (measured by the terms of partial R 2 exposure and R 2 outcome ) are both less than the RV, then the confounder cannot "explain away" the observed association [21] . Because it is difficult to determine what an ideal RV value should be, we calculated a benchmark range based on the established covariate "race", which is known to be strongly associated with RMC diagnosis. Analysis was performed using Stata/SE v16.1 (StataCorp, College Station, TX). Data were graphed using GraphPad. Variables were compared between RMC and matched control patients using Wilcoxon rank-sum or Fisher's exact tests. Two-way ANOVA and Tukey multiple comparison tests were used to compare the changes in HIF1α-luciferase activity for exercise experiments. 

A total of 71 patients with RMC were compared to 122 control patients (Table 1,  Supplementary Tables S1-S3) . We were unable to find suitable matched control patients for 4 RMC patients, and 12 patients were matched 1:1. All patients with RMC had a sickle hemoglobinopathy (predominantly SCT), the majority were male (69%) and of African descent (86%), and the primary tumor was located in the right kidney three times more frequently (76%) than the left (Table 1, Supplementary Table S1 ). Compared with matched controls, patients with RMC had significantly higher rates of positive activity index, reported exercise, athletic involvement, and military service ( Table 1) . Additionally, patients with RMC had significantly poorer ECOG performance status compared to controls (Table 1) . We evaluated the albumin levels obtained at the time of diagnosis as a surrogate measure of cachexia [22] [23] [24] . No significant difference in albumin level was found between RMC and control patients ( Table 1 ). SM surface area was significantly higher in patients with RMC (median 59.3 cm 2 /m 2 , IQR 50.2-69.9 cm 2 /m 2 ) compared with controls (median 52.4 cm 2 /m 2 , IQR 45.0-59.1 cm 2 /m 2 ) (p = 0.001) (Figure 1a ,b). Our multivariable models adjusting for confounders identified on SCMs (race, age, and sex) demonstrated a significant relationship between physical activity index and RMC diagnosis (OR 10.4, 95% CI 4.5-23.9, p < 0.001), as well as between higher SM surface area and RMC diagnosis (OR 1.04, 95% CI 1.00-1.09, p = 0.03) (Figure 1c , Supplementary Tables S4 and S5). Conditional multivariable logistic regression models again demonstrated a significant relationship between physical activity index and RMC diagnosis (OR 8.9, 95% CI 3.05-26.1, p < 0.001) as well as SM surface area and RMC diagnosis (OR 1.02, 95% CI 1.01-1.04, p = 0.02). Although it was not identified as a potential confounder (Supplementary Figure S1 ), we performed a sensitivity analysis where albumin, a surrogate for cachexia [22] , was included as a covariate in our multivariable model for SM, and SM remained significantly associated with RMC diagnosis (Supplementary Table S6 ). The addition of smoking as another potential confounder in our multivariable regression models did not change the significant association between both activity index and SM with RMC diagnosis (Supplementary  Tables S7 and S8 ). No significant difference was found in subcutaneous adipose surface area (p = 0.2), suggesting no marked difference in nutritional status between the RMC and control cohorts. Consistent with our retrospective findings, prospective evaluation of patients with RMC demonstrated that the majority of patients (71%) reported frequent, high-intensity exercise defined as ≥80% of maximal heart rate during each exercise session (Supplementary Tables S9 and S10). 

Because unexplained variables may exist that could confound the relationship between activity index and RMC diagnosis, we quantified how strong such unmeasured confounders would need to be to "explain away" the association of activity index with RMC diagnosis. Our multivariable regression model demonstrated a large robustness value (RV) of 39% for the activity index. This means that confounders explaining less than 39% of the residual variance of both the exposure and outcome would not be strong enough to nullify the estimated effect of physical activity on RMC diagnosis. Race is a powerful known confounder adjusted for in our regression model. If we wanted to identify putative unmeasured confounding variables as strong as race, their total effect would be bound by the limits of partial R 2 exposure = 11% to R 2 outcome = 23%. Based on the RV for activity index, the effect of all unmeasured confounding variables would need to be over two times stronger than the effect of race in order to explain away the statistically significant association of activity index with RMC diagnosis (Supplementary Figure S2a-c) .

We validated these findings in a separate epidemiologic comparison group by looking at the proportion of all black individuals with SCT who serve in the U.S. military, hypothesizing that the intense physical activity of military duty may increase the risk of RMC. Details on the population estimate can be found in the Supplementary Methods under the section "Epidemiologic comparison". We found that a higher proportion (OR 8.4, 95% CI 3.2-18.4, p < 0.0001) of black patients with RMC (7/61, 11%) had served in the U.S. military than would be expected compared to the similarly-aged black population with SCT in the U.S. (17,816/1165, 297, 1.5%) (Figure 1d ).

GEMMs of SCT were generated to selectively express a TdTomato (TdT) fluorescence reporter in the kidney epithelium (Figure 2a) . Pathological evaluation demonstrated RBC sickling in the renal medulla (Figure 2b ) but not in the peripheral blood (Supplementary Figure S3 ) consistent with the clinical observation that the renal medullary microenvironment is conducive to RBC sickling in individuals with SCT. To measure hypoxia in the renal medulla, we injected the Hypoxyprobe, which confirmed the presence of hypoxia in the renal inner medulla of SCT mice compared with wild-type controls (p < 0.0001) (Figure 2c,d) . Renal hypoxia measured by the Hypoxyprobe was most pronounced in the right kidney of GEMM with SCT ( Figure 2d ).

To test whether increasing the intensity of exercise would worsen renal hypoxia among SCT mice, we generated a GEMM of SCT by crossing the hα/hα::β S /β S strain with the Gt(ROSA)26Sor tm2(HIF1A/luc)Kael strain, allowing non-invasive monitoring of HIF1α activity in response to hypoxia by measuring luciferase activity using IVIS (Figure 3a ) [25] . We evaluated wild-type and SCT mice at moderate and high (Figure 3b ,c) treadmill exercise intensities, as previously established [17] . Luciferase fluorescence was measured before exercise, immediately after exercise, and after one hour of rest (Figure 3d ,e). When exposed to moderate-intensity exercise (Figure 3d) , there was a significant decrease in HIF1α activation in the SCT mice for both the left (p = 0.048) and right (p = 0.02) kidneys. There was no significant change in wild-type mice. High-intensity exercise (Figure 3e) , however, resulted in significantly higher HIF1α activation among SCT mice compared to wild-type (p = 0.005), which was most pronounced within the right kidney (p = 0.04). The higher tissue hypoxia in the right kidney of SCT mice in the setting of high-intensity exercise corresponded to the predilection of the right kidney in humans towards hypoxia due to the longer length of the right renal artery [3] . As in humans, we found that the right renal artery length in the C57BL/6J mixed background mice used in our study was longer than the left (Figure 3f,g) . due to the longer length of the right renal artery [3] . As in humans, we found that the right renal artery length in the C57BL/6J mixed background mice used in our study was longer than the left (Figure 3f,g) . The CDH16 Cre strain was crossed with the conditional Rosa26 LSL-TdT strain and the hα/hα::β S /β S strain to generate a GEMM of SCT (hα/hα::β A /β S ) that allows for tissue specific activation of TdTomato (TdT) fluorescence reporter in the kidney epithelium. (B) Hematoxylin and eosin staining of kidney tissue from wild-type mice (upper) and mice with SCT (lower). Sickle morphology is apparent in mice with SCT. Sickled RBCs have spindle-like morphology and are indicated with yellow arrows. (C) Hypoxyprobe (pimonidazole hydrochloride) was injected in the intraperitoneal cavity of GEMM of SCT with kidney-specific CDH16 Cre and conditional R26 LSL-Tom three hours prior to euthanasia and harvesting of kidneys. Kidneys were processed, and immunohistochemistry with the Hypoxyprobe antibody was used to show hypoxia in the inner medulla of wild-type mice (left column) and mice with SCT (right column). (D) Quantification of the optical density of Hypoxyprobe staining for 20x images was carried out using ImageJ. The CDH16 Cre strain was crossed with the conditional Rosa26 LSL-TdT strain and the hα/hα::β S /β S strain to generate a GEMM of SCT (hα/hα::β A /β S ) that allows for tissue specific activation of TdTomato (TdT) fluorescence reporter in the kidney epithelium. (B) Hematoxylin and eosin staining of kidney tissue from wild-type mice (upper) and mice with SCT (lower). Sickle morphology is apparent in mice with SCT. Sickled RBCs have spindle-like morphology and are indicated with yellow arrows. (C) Hypoxyprobe (pimonidazole hydrochloride) was injected in the intraperitoneal cavity of GEMM of SCT with kidney-specific CDH16 Cre and conditional R26 LSL-Tom three hours prior to euthanasia and harvesting of kidneys. Kidneys were processed, and immunohistochemistry with the Hypoxyprobe antibody was used to show hypoxia in the inner medulla of wild-type mice (left column) and mice with SCT (right column). (D) Quantification of the optical density of Hypoxyprobe staining for 20x images was carried out using ImageJ. Comparisons were made between wild-type and SCT mice and stratified by kidney laterality within SCT (left kidneys, n = 8; right kidneys, n = 18) and wild-type (left kidneys, n = 16; right kidneys, n = 26) mice. Data are expressed as mean value ± SD, with p value calculated by student's t test.

Comparisons were made between wild-type and SCT mice and stratified by kidney laterality within SCT (left kidneys, n = 8; right kidneys, n = 18) and wild-type (left kidneys, n = 16; right kidneys, n = 26) mice. Data are expressed as mean value ± SD, with p value calculated by student's t test. HIF1α oxygen-dependent degradation domain fused to firefly luciferase, allowing non-invasive monitoring of HIF1α activity in response to hypoxia using the in vivo imaging system (IVIS). The hα/hα::β S /β S strain was crossed with the Gt(ROSA)26Sor tm2(HIF1A/luc)Kael strain. (B,C) IVIS imaging of wild-type (n = 11) and SCT (n = 10) mice harboring the HIF1α oxygen-dependent degradation domain fused to firefly luciferase before moderate-intensity exercise (B) and highintensity exercise (C), immediately after, and after one hour of rest. (D,E) Intensity of HIF1α-luciferase activity after moderate-intensity exercise (D) and high-intensity exercise (E). Two-way ANOVA and Tukey multiple comparison tests were used to calculate the p values of the changes in HIF1α-luciferase activity in adult SCT (n = 10) and wild-type (n = 11) HIF1α oxygen-dependent degradation domain fused to firefly luciferase, allowing non-invasive monitoring of HIF1α activity in response to hypoxia using the in vivo imaging system (IVIS). The hα/hα::β S /β S strain was crossed with the Gt(ROSA)26Sor tm2(HIF1A/luc)Kael strain. (B,C) IVIS imaging of wild-type (n = 11) and SCT (n = 10) mice harboring the HIF1α oxygen-dependent degradation domain fused to firefly luciferase before moderate-intensity exercise (B) and high-intensity exercise (C), immediately after, and after one hour of rest. (D,E) Intensity of HIF1α-luciferase activity after moderateintensity exercise (D) and high-intensity exercise (E). Two-way ANOVA and Tukey multiple comparison tests were used to calculate the p values of the changes in HIF1α-luciferase activity in adult SCT (n = 10) and wild-type (n = 11) mice after exercise and rest. (F) Gross anatomy of C57BL/6J mixed background mouse showing difference in the lengths between the right and left renal arteries. (G) Quantified difference in the length of left and right renal arteries from six adult C57BL/6J mixed background mice. Data are expressed as mean value ± SD, with p value calculated by student's t test.

Given the lethality of RMC, it is essential to identify modifiable risk factors that can inform future prevention strategies. Our clinical observations of frequently reported high-intensity exercise among our RMC patient population led us to hypothesize that highintensity exercise may play a critical role in the pathogenesis of RMC. Our case-control analysis supports this hypothesis by demonstrating higher reported physical activity and objectively measured SM surface area among patients with RMC compared to matched controls. Additionally, we found significantly higher proportions of military service among patients with RMC compared to the general U.S. population of black SCT individuals. Our mouse models of SCT provide additional preclinical evidence of the consequence of high-intensity exercise on renal hypoxia in the setting of SCT, particularly in the right kidney, which is most frequently affected by RMC. Our experimental GEMM results suggest that moderate-intensity exercise is not harmful and may mitigate renal hypoxia, while increasing the intensity of exercise exacerbates renal hypoxia in SCT. These findings support human studies recommending low/moderate intensity exercise training to reduce complications related to sickle hemoglobinopathies [26, 27] .

No familial clustering of RMC has been reported to date, and a recent study of germline and somatic haplotypes in 14 unrelated patients with RMC harboring the sickle cell trait found no germline alleles or alterations in cancer predisposition genes or genes affecting kidney injury associated with RMC [28] . This suggests that environmental rather than genetic risk factors may interact with sickle hemoglobinopathies in patients with RMC. Our study is the first to suggest that increased renal hypoxia due to high-intensity exercise is a risk factor for RMC. While prior studies have evaluated the clinical characteristics, molecular landscape, and treatment outcomes of RMC, there is little evidence regarding potential modifiable risk factors for RMC [29] [30] [31] [32] [33] [34] [35] [36] . The exact mechanism linking renal medullary hypoxia to tumorigenesis, and loss of the SMARCB1 tumor suppressor in particular, remains to be determined. We have previously provided a testable conceptual model of how renal medullary hypoxia induced by RBC sickling can activate low-fidelity DNA repair mechanisms that can specifically induce the SMARCB1 deletions and translocations found in RMC tissues [3, 36] . The significantly increased renal medullary hypoxia found in our GEMMs in the setting of high-intensity exercise will allow more detailed investigation and refinement of the sequential molecular steps involved in RMC pathogenesis.

In the retrospective portion of our study, our matching of patients with RMC focused on ensuring similar cancer stage, age, and biologic sex between the two populations. An internal control of the utility of comparing our RMC cohort with their matched controls is that it reproduced the well-established associations between RMC and the presence of sickle hemoglobinopathies, as well as the high incidence of RMC among African Americans (Table 1 ) [2] . It also notably suggested that smoking is more frequently observed among patients with other genitourinary malignancies, many of which have previously established strong associations with smoking [37] [38] [39] . Furthermore, multivariable analyses adjusting for the racial imbalance between the RMC and matched controls confirmed the association of both increased skeletal muscle and reported exercise history with RMC diagnosis. Future efforts will focus on prospectively evaluating the type, duration, and intensity of exercise activities among patients with RMC and matched controls with SCT.

Our GEMMs provide the first evidence of the nature of this interaction by showing that only high-intensity exercise aggravates renal hypoxia in the setting of SCT. Because mouse models of RMC have not been developed to date, the exact steps of RMC pathogenesis remain to be elucidated. It is possible that the relationship between RMC and SCT is purely associative in nature and/or that hypoxic damage in the renal medulla induced by the sickling of RBCs is not the major driver of RMC pathogenesis. In that case, an alternative confounding causal mechanism would need to explain the distinct clinical features of RMC, such as the strong association with all sickle hemoglobinopathies and the distinct predilection towards the right kidney. These features are parsimoniously explained by renal medullary hypoxia due to RBC sickling being the key event of RMC pathogenesis, as represented in Supplementary Figure S1 [3] . This model predicts that any causes of increased renal hypoxia in the setting of SCT, such as high-intensity exercise as confirmed for the first time in our mouse models, can increase the risk of RMC. A putative alternative mechanism must also explain our clinical retrospective and prospective observations, which consistently demonstrated an association between high-intensity exercise and RMC. Even if RMC pathogenesis is not driven by increased hypoxia due to RBC sickling, the results of the present study would still serve as a body of clinical, epidemiologic, and animal modeling observations requiring explanation by proposed alternative causal theories [40] . We quantified how strong unmeasured putative confounders would need to be to remove the observed association between the activity index and RMC, using race as a reference because it is the strongest identifiable confounder between our RMC and matched cohorts. Our results suggest that, even if confounding variables two times stronger than race were missed from our regression analysis, this would still not account for the observed significant association between physical activity and RMC diagnosis (Supplementary Figure S2) .

From a clinical practice standpoint, our findings support the current safe exercise recommendations by the Centers for Disease Control and Prevention (CDC), the National Athletic Trainers' Association (NATA), and the National Collegiate Athletic Association (NCAA) towards athletes with SCT, their coaches, and physicians [41] [42] [43] [44] [45] . These recommendations were generated due to the association between SCT and rhabdomyolysis or cardiovascular collapse in the setting of high-intensity exercise and endorse more moderate training regimens. Our findings provide no clinical evidence that moderate-intensity exercise is associated with RMC, and our animal models suggest that such exercise may reduce renal hypoxia in addition to the many other health benefits of exercise. Our study suggests that RMC should be high on the differential in young individuals with SCT presenting with a kidney mass and a history of high-intensity exercise or increased skeletal muscle mass on CT imaging. These associations may help inform future screening strategies for RMC by focusing on those individuals more likely to be diagnosed with this disease.

The major limitations of the clinical portion of this study are its retrospective observational nature and single center design. Additionally, given the rarity of RMC, our prospective cohort included only seven patients with exercise evaluation. Motivated by the present findings, further prospective multi-institutional evaluation of the association between exercise intensity and RMC is warranted. Another limitation is that four patients with RMC were unable to be matched. Matching patients with RMC to similarly aged patients with advanced genitourinary tumors seen in the same department and time period is challenging given the young age at which RMC affects individuals. Our inferences are strengthened by the multiple approaches we used to triangulate our findings and potentially refute our hypothesis. The retrospective evaluation of physical activity would be similarly biased in the RMC and matched controls as it was evaluated using the same approach (retrospective evaluation of the same binary activity score) over the same time period in a single department. These subjective reports were complemented by objective measures of SM surface area, which again showed significantly higher levels among patients with RMC compared to controls. This signal persisted after controlling for confounders including race, age, gender, and smoking. We additionally considered whether cachexia could have biased our findings. If that was the case, the results would have been biased against our hypothesis, because RMC is one of the deadliest genitourinary malignancies, with sarcopenia quickly manifesting following diagnosis [2, 7] . This distinct aggressiveness is reflected by the significantly worse performance status we found in patients with RMC compared with matched controls. SCMs revealed performance status to be a collider (Supplementary Figure S1) , and this variable was omitted from multivariable regression analyses to prevent introduction of collider bias [18, 19] . In addition, serum albumin, which is associated with cachexia and mortality [23, 24] , was similar between our RMC and matched controls and when adjusted for, did not impact the association between SM and RMC diagnosis. Furthermore, to avoid therapy effects on anthropometric measures, all imaging used to quantify muscle and adipose tissue was obtained prior to the initiation of systemic therapy. When we began to prospectively interrogate additional patients with RMC, which allowed more granular evaluation of physical activity compared with the binary activity score of our retrospective cohort, a pattern of high-intensity exercise in the majority of patients was observed. The association between RMC and high-intensity exercise was also found when we performed an epidemiologic analysis of military service.

We supplemented these clinical observations with mouse models developed to test our hypothesis that high-intensity exercise will increase renal medullary hypoxia. We found that renal medullary hypoxia significantly increased predominantly in the right kidney following high-but not moderate-intensity exercise, consistent with the distinct predilection of RMC toward the right kidney in humans [3] . The major limitation of our GEMM experiments is that they did not directly lead to RMC tumors. This is not unexpected given the rarity of RMC. If the biological context in our GEMMs parallels that of humans, we would anticipate that less than 1% of the mice with SCT would develop RMC, even after chronic exposure to high-intensity exercise.

In conclusion, our data suggest that high-intensity exercise may be a risk factor for developing RMC in individuals with SCT. Prospective multi-institutional studies are warranted to validate these findings and elucidate the impact of specific exercise regimens on RMC risk. These findings should be considered when counseling and monitoring individuals with SCT, particularly those occupationally engaged in high-intensity exercise.

Supplementary Materials: The following are available online at https://www.mdpi.com/article/10.3 390/cancers13236022/s1, Supplementary methods, Figure S1 : Structural causal models, Figure S2 : Sensitivity plots, Figure S3 : Peripheral red blood cell smear comparing wild-type and sickle cell trait mice, Table S1: Additional clinical characteristics of patients with RMC, Table S2 : Metastatic locations among patients with RMC and metastatic disease at initial diagnosis, Table S3 : Cancer type and stage for matched control patients, Table S4 : Full multivariable model evaluating association between physical activity index and diagnosis of RMC, Table S5 : Full multivariable model evaluating association between standardized skeletal muscle surface area and diagnosis of RMC, Table S6 : Multivariable model including albumin evaluating the association between standardized skeletal muscle surface area and diagnosis of RMC, Table S7 : Multivariable model including smoking evaluating the association between physical activity index and diagnosis of RMC, Table S8 : Multivariable model including smoking evaluating the association between standardized skeletal muscle surface area and diagnosis of RMC, Table S9 : Clinical characteristics of prospectively evaluated patients with RMC, Table S10 : Prospectively collected exercise history of seven patients with RMC. Institutional Review Board Statement: This study was conducted according to the guidelines of the Declaration of Helsinki and approved by the MD Anderson institutional review board (protocol numbers PA11-1045 and PA16-0736). All animal studies were approved by the IACUC at MD Anderson Cancer center in accordance with NIH guidelines.

Renal medullary carcinoma-The 7th sickle-cell nephropathy

Updated Recommendations on the Diagnosis, Management, and Clinical Trial Eligibility Criteria for Patients with Renal Medullary Carcinoma

A Model Linking Sickle Cell Hemoglobinopathies and SMARCB1 Loss in Renal Medullary Carcinoma

Public health implications of sickle cell trait: A report of the CDC meeting

Renal medullary carcinoma and sickle cell trait: A systematic review. Pediatr

Systemic Therapies for the Management of Non-Clear Cell Renal Cell Carcinoma: What Works, What Doesn't, and What the Future Holds

Management and outcomes of patients with renal medullary carcinoma: A multicentre collaborative study

Sickle cell nephropathy

The carrier state for sickle cell disease is not completely harmless

Balancing exercise risk and benefits: Lessons learned from sickle cell trait and sickle cell anemia

Guide to the assessment of physical activity: Clinical and research applications: A scientific statement from the american heart association

Differentiating Sarcopenia and Cachexia Among Patients with Cancer

The Effects of Neoadjuvant Axitinib on Anthropometric Parameters in Patients with Locally Advanced Non-metastatic Renal Cell Carcinoma

Demographics Report: Profile of the Military Community

Physiological adaptations to interval training and the role of exercise intensity

Oxygen consumption in adult and aged C57BL/6J mice during acute treadmill exercise of different intensity

Causal Diagram Techniques for Urologic Oncology Research

Collider bias undermines our understanding of COVID-19 disease risk and severity

Robust causal inference using directed acyclic graphs: The R package 'dagitty'

Making sense of sensitivity: Extending omitted variable bias

Cachexia in cancer: What is in the definition?

The clinical picture of cachexia: A mosaic of different parameters (experience of 503 patients)

The prognostic role of inflammation and hormones in patients with metastatic cancer with cachexia

Mouse model for noninvasive imaging of HIF prolyl hydroxylase activity: Assessment of an oral agent that stimulates erythropoietin production

Exercise training blunts oxidative stress in sickle cell trait carriers

Haplotype-resolved germline and somatic alterations in renal medullary carcinomas

Balanced Translocations Disrupting SMARCB1 Are Hallmark Recurrent Genetic Alterations in Renal Medullary Carcinomas

Genomic Characterization of Renal Medullary Carcinoma and Treatment Outcomes

Renal medullary carcinomas depend upon SMARCB1 loss and are sensitive to proteasome inhibition

Distinctive mechanisms underlie the loss of SMARCB1 protein expression in renal medullary carcinoma: Morphologic and molecular analysis of 20 cases

Molecular hallmarks of renal medullary carcinoma: More to c-MYC than meets the eye

Efficacy and Safety of Bevacizumab Plus Erlotinib in Patients with Renal Medullary Carcinoma

Efficacy and safety of gemcitabine plus doxorubicin in patients with renal medullary carcinoma

Comprehensive Molecular Characterization Identifies Distinct Genomic and Immune Hallmarks of Renal Medullary Carcinoma

Association between smoking and risk of bladder cancer among men and women

The role of tobacco smoke in bladder and kidney carcinogenesis: A comparison of exposures and meta-analysis of incidence and mortality risks

Latest Evidence on the Impact of Smoking, Sports, and Sexual Activity as Modifiable Lifestyle Risk Factors for Prostate Cancer Incidence, Recurrence, and Progression: A Systematic Review of the Literature by the European Association of Urology Section of Oncological Urology (ESOU)

The value of risk-factor

Athletes: Don't Get Sidelined by Sickle Cell Trait! Play It Safe with These Helpful Tips

Coaches: Don't Let Your Athletes Get Sidelined by Sickle Cell Trait! Help Them Play It Safe with These Helpful Tips

Fact Sheet: Team Doctors (Trainers): Don't Let Your Athletes Get Sidelined by Sickle Cell Trait! Help Them Play It Safe with These Helpful Tips

Fact Sheet for Student-Athletes: Sickle Cell Trait

National Athletic Trainers' Association Consensus Statement: Sickle Cell Trait and the Athlete

Conflicts of Interest: P.M. has received honoraria for service on scientific advisory boards for Mirati Therapeutics, Bristol-Myers Squibb, and Exelixis, consulting for Axiom Healthcare Strategies, nonbranded educational programs supported by Exelixis and Pfizer outside this submitted work, and research funding for clinical trials from Takeda, Bristol-Myers Squibb, Mirati Therapeutics, Gateway for Cancer Research, and UT MD Anderson Cancer Center, all outside this submitted work. A.Y.S. has received honoraria for service on scientific advisory boards for Bristol-Myers Squibb, Eisai, and EMD Serono, as well as research funding from Exelixis, Bristol-Myers Squibb, Pfizer, and Roche, outside this submitted work. N.M.T. has received honoraria for service on Scientific Advisory Boards for Bristol-Myers Squibb, Eli Lilly and Company, Exelixis, Inc., and Nektar Therapeutics; for strategic council meetings with Eisai Inc.; steering committee meetings with Pfizer, Inc.; and for seminar presentations for Ono Pharmaceutical Co., Ltd.; as well as research funding for clinical trials from Exelixis, Inc., Calithera Biosciences, and Nektar Therapeutics, outside the submitted work. C.L. has received honoraria from Bayer, Exelixis, Merck Sharp & Dohme, and Amgen, consulting fees from Bayer, Merck Sharp & Dohme, and Amgen, as well as research funding from Astellas Pharma, Bristol-Myers Squibb, Bayer, Novartis, Janssen and Pfizer, all outside the submitted work. J.A.K. has received honoraria for service on Scientific Advisory Boards for Pfizer, Merck, and Roche/Genentech; institutional research funding from Roche/Genentech, Mirati Therapeutics, Merck, and Elypta; and holds stock ownership from Allogene, MedTek, and ROM technologies. All remaining authors have declared no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

Cancers 2021, 13, 6022 13 of 15 Informed Consent Statement: Informed consent was obtained from all patients with RMC involved in the study. Informed consent was waived for the matched control patients due to the retrospective nature of the study and the analysis used anonymous clinical data.Data Availability Statement: Data may be accessed from the corresponding authors upon reasonable request.