Researchers discover novel mechanism linking changes in mitochondria to cancer cell death | News | Notre Dame News | University of Notre Dame Skip To Content Skip To Navigation Skip To Search University of Notre Dame Notre Dame News Experts ND in the News Subscribe About Us Home Contact Search Menu Home › News › Researchers discover novel mechanism linking changes in mitochondria to cancer cell death Researchers discover novel mechanism linking changes in mitochondria to cancer cell death Published: March 16, 2018 Author: Deanna Csomo McCool Zach Schafer And Mark Hawk 1200 Feature To stop the spread of cancer, cancer cells must die. Unfortunately, many types of cancer cells seem to use innate mechanisms that block cancer cell death, therefore allowing the cancer to metastasize. While seeking to further understand cancer cell death, Notre Dame researchers discovered that the activation of a specific enzyme may help suppress the spread of tumors. The findings, published in Nature Cell Biology, demonstrate that the enzyme RIPK1 decreases the number of mitochondria in a cell. This loss of mitochondria leads to oxidative stress that can potentially kill cancer cells, though researchers speculate the cancer cells could find ways to shut down this effect. During the study, the Notre Dame team discovered that when the enzyme RIPK1 is activated in a cell, it can cause the number of mitochondria — considered the “power plants” of the cell — to decrease as the cell consumes its own components for energy, a process called mitophagy. This was surprising, given RIPK1 was well-known to regulate necrosis, a completely distinct cell death mechanism.  “We really thought this was going to be a story about necrosis, but we weren’t able to see evidence of it, and knew there had to be something we’re missing,” said Zachary Schafer, Coleman Foundation Associate Professor of Cancer Biology in the Department of Biological Sciences and senior author on the study. “Looking at mitochondrial numbers fundamentally changed our thinking, and got us focused on a different way that RIPK1 may cause cells to die.” Schafer focuses on metastasis, the process by which cancer cells leave the primary tumor and disseminate to other parts of the body. Cell death, a barrier to metastasis, can be induced when epithelial cells, those lining the surfaces of body cavities, detach from the meshwork of scaffolding-like proteins called the extracellular matrix (ECM). As a tumor progresses, it can become resistant to this type of cell death. “While our findings are in their infancy, we hope we can take advantage of the liability associated with RIPK1’s function in order to design a strategy aimed at eliminating ECM-detached cancer cells, which would ultimately improve patient survival,” said Mark Hawk, a graduate student at Notre Dame and lead author of the study. Hawk added that more studies are needed to delineate which cancer types are most susceptible to this approach. Co-authors on the study include Cassandra Gorsuch, Joshua Mason, Kelsey Weigel, Matyas Abel Tsegaye, Junjun Zuo, Patrick Fagan, Luqun Shen, Stephan Hu, Sarah Chapman, and W. Matthew Leevy at the Notre Dame Integrated Imaging Facility, as well as researchers from Beckman Research Institute of City of Hope, Memorial Sloan Kettering Cancer Center, University of Texas Southwestern Medical Center and Weill Cornell Medical College. The research was funded by the National Science Foundation, the Coleman Foundation, the American Cancer Society and the Phi Beta Psi National Project. Contact: Jessica Sieff, assistant director, media relations, 574-631-3933, jsieff@nd.edu Originally published by Deanna Csomo McCool at news.nd.edu on February 19, 2018. Home Experts ND in the News Subscribe About Us For the Media Contact Office of Public Affairs and Communications Notre Dame News 500 Grace Hall Notre Dame, IN 46556 USA Facebook Twitter Instagram YouTube Pinterest © 2022 University of Notre Dame Search Mobile App News Events Visit Accessibility Facebook Twitter Instagram YouTube LinkedIn