News Release

Protein identified which helps cancer cells to survive stressful conditions

Peer-Reviewed Publication

PLOS

Researchers at NUI Galway have made a discovery that could lead to the development of more effective treatments for a number of diseases. They have shown that a protein produced when cells are stressed interacts with a stress sensor allowing cells to survive conditions of intense stress. Understanding this interaction may help scientists interfere with cancer cells so the cells can no longer survive exposure to stressful conditions. These findings are published next week in the online, open access journal PLoS Biology.

Healthy cells are not usually under stress, but unhealthy cells, such as cancer cells, are often under considerable stress because they grow rapidly in places where they are not supposed to grow. When a cell is under these stressful conditions, the stress protein Hsp70 is activated to help the cell.

Professor Afshin Samali, lead author of the study and head of the Department of Biochemistry at NUI Galway, and his team have discovered that under cell stress conditions Hsp70 interacts with a receptor in the cell, activating survival mechanisms and preventing apoptosis, the normal cell death mechanism. By understanding more about Hsp70 and the way it functions, scientists can learn how to block its function, allowing unhealthy cells to succumb to stress and die. This could have significant implications in the development of new cancer drugs, which would block the protein to encourage tumor cell death. In contrast to diseases where cell death is abundant such as Alzheimer's, Parkinson's Disease, and Diabetes, increasing the levels of Hsp70 could potentially be used to help these cells survive stressful conditions.

Professor Samali states: "Our results have identified a novel protein-protein interaction that helps cancer cells to survive stressful growth conditions. By interfering with this interaction we hope to develop a new class of anticancer drugs. This work was funded by Science Foundation Ireland and will have a significant impact on cancer research and drug design."

###

Funding: This publication has emanated from research conducted with the financial support of Science Foundation Ireland under grant number 06/RFP/BIC002, 05/IN3/B851 (to AS); and Enterprise Ireland, and FONDECYT no. 1100176 (to CH), FONDAP grant no. 15010006, Millennium Nucleus no. P07-048-F, and ICGEB (CH); CONICYT fellowship (FL). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests statement: The authors declare that no competing interests exist.

Citation: Gupta S, Deepti A, Deegan S, Lisbona F, Hetz C, et al. (2010) HSP72 Protects Cells from ER Stress-induced Apoptosis via Enhancement of IRE1a-XBP1 Signaling through a Physical Interaction. PLoS Biol 8(7): e1000410. doi:10.1371/journal.pbio.1000410

PLEASE ADD THE LINK TO THE PUBLISHED ARTICLE IN ONLINE VERSIONS OF YOUR REPORT: http://biology.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pbio.1000410

PRESS ONLY PREVIEW OF THE ARTICLE: http://www.plos.org/press/plbi-08-07-Samali.pdf

CONTACT:
Michelle Ni Chroinin
Press & Information Officer
NUI Galway
+353 91 493542
michelle.nichroinin@nuigalway.ie


Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.