Roanoke Times Copyright (c) 1995, Landmark Communications, Inc. DATE: THURSDAY, April 14, 1994 TAG: 9404140344 SECTION: NATIONAL/INTERNATIONAL PAGE: A3 EDITION: METRO SOURCE: Associated Press DATELINE: SAN FRANCISCO LENGTH: Medium
Loss of the gene was detected in a broad range of cancers, including 60 percent of breast cancer cases and 82 percent of one type of brain tumor.
``It's very close to the action of cell division. When it's broken, destroyed, mutated, cell division is left out of control,'' said Dr. Mark Skolnik of the University of Utah Medical Center.
The newly identified tumor-suppressing gene, p16, appears even more significant that the previously identified p53 gene, which is believed to be a major factor in colon, breast, liver and other cancers, said Alexander Kamb of Utah-based Myriad Genetics Inc., who helped lead the p16 research.
P16 controls the production of an enzyme that inhibits cell growth in cancer genes, while p53 does not, he said.
Cancer researchers are increasingly turning their attention to suppressor genes, which brake uncontrolled cell division.
Damage to these suppressor cells - by chemicals in cigarette smoke, ultraviolet light, radiation or other carcinogens - may be the chief cause of cancer, Kamb said at the annual meeting of the American Association for Cancer Research in San Francisco.
P16 may "looks really promising as a major player in human cancers,'' he said.
Discovery of the p16 gene - called MTS1 by the Utah team - was first announced by David Beach of Cold Spring Harbor Laboratory in New York late last year.
The Utah team researched the gene's role in fighting tumors and is publishing its findings in the April 15 issue of Science.
by CNB