How protein forces ovarian cancer cells to kill themselvesNovember 16th, 2008 - 4:53 pm ICT by ANI
Washington, Nov 16 (ANI): Researchers at the University of Texas M. D. Anderson Cancer Center have found that a protein, known to inhibit the growth of ovarian cancer, works in part by forcing cancer cells to eat themselves until they die.
Senior author Naoto T. Ueno, M.D., Ph.D. associate professor of breast medical oncology, said that the researchers also found that expression of the protein, known as PEA-15, is an independent indicator of a woman’’s prospects for surviving ovarian cancer.
An analysis of ovarian cancer tumours from 395 women showed those with high expression of the PEA-15 had a median survival time of 50.2 months compared with 33.5 months for women with low levels of the protein in their tumours.
“These findings provide a foundation for developing a PEA-15 targeted approach for ovarian cancer and for clarifying whether this protein is a novel biomarker that can predict patient outcomes,” Ueno said.
A series of lab experiments by first author Chandra Bartholomeusz, M.D., Ph.D., showed that high expression of PEA-15 inhibits the growth of ovarian cancer cells by killing cells via autophagy, or self-cannibalization, rather than by apoptosis.
Removing PEA-15 from ovarian cancer cells led to a 115 percent increase in the number of cells compared with a control group of cells that still had the protein.
In apoptosis, defective cells die from self-induced damage to their nuclei and DNA complex. Autophagy kills when a cell entraps parts of its cytoplasm in membranes and digests the contents, leaving a cavity. When this goes on long enough, the cell essentially eats itself until it dies, its cytoplasm riddled with cavities.
The research team has found that the protein works to inhibit cancer in two distinct ways depending on its location in the cell.
First, PEA-15 inhibits one of the prominent actors in the growth, differentiation and mobility of cells, a protein called extracellular signaling related kinase, or ERK. Activated ERK in the cell nucleus fuels cancer growth.
Earlier, the research team found that PEA-15 binds to ERK in the nucleus and moves it out into the cytoplasm, preventing its growth effects.
Now, they”ve found that PEA-15 in the cytoplasm induces autophagy in cancer cells, a second method of inhibiting cancer growth.
“These two very different actions by PEA-15 are based on the location of the protein,” Ueno said.
Ueno said that ERK is an inviting target for cancer therapy but so far no one has been able to develop a successful ERK inhibitor.
“PEA-15 offers us a new dimension for potentially targeting ERK. We”ve shown with high levels of PEA-15, women with ovarian cancer are surviving longer,” Ueno said.
The study is published in the Nov. 15 issue of Cancer Research. (ANI)
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Tags: anderson cancer center, autophagy, biomarker, cancer cells, cancer tumours, cannibalization, control group, cytoplasm, defective cells, kinase, lab experiments, m d anderson, m d anderson cancer center, median survival, medical oncology, ovarian cancer, patient outcomes, survival time, ueno, university of texas m d anderson cancer center