La Jolla (California): A study performed by Sanford Burnham Prebys researchers discovered that specific genetic abnormalities are linked to treatment-resistant breast cancer in young women. These mutations do not appear to be associated with treatment-resistant breast cancer in older women.
The findings, published in the journal Science Advances, could help improve precision medicine and suggest a brand-new way of classifying breast cancer.
"It's well established that as you get older, you're more likely to develop cancer. But we're finding that this may not be true for all cancers depending on a person's genetic makeup," said senior author Svasti Haricharan, Ph.D., an assistant professor at Sanford Burnham Prebys, adding, "There may be completely different mechanisms driving cancer in younger and older people, which requires adjusting our view of aging and cancer."
The study concentrated on ER+/HER2- breast cancer, which is one of the most frequent types of the illness. It is often treated with hormonal therapy, although these treatments do not work for many people. Approximately 20 percent of tumours reject therapy from the start, and up to 40 per cent acquire resistance over time.
"Understanding how certain forms of breast cancer develop in a way that makes them eventually resist therapy can help us better classify the disease. It may also help clinicians adjust the treatment plans for patients who will likely experience resistance to standard treatments," said Haricharan, adding, "For scientists like myself, it can help guide research to develop new therapies to overcome these obstacles."
The study included an extensive analysis of a large database of breast cancer patients. It revealed that in ER+/HER2- breast cancer patients, certain gene mutations had a strong correlation with response to treatment--and the effects were dependent on age. Some gene mutations were only linked with treatment-resistant breast cancer in younger women.
"This was a strange finding, so much so that we almost didn't believe it at first," said Haricharan, adding, "But the same patterns emerged over and over again in database after database."
The mutations the researchers identified were in genes involved in cell replication, the process by which cells grow and divide. These genes are responsible for repairing mistakes when they happen--a process that goes awry in virtually all cancers.
"Cell cycle dysregulation occurs so early in the development of cancer that we generally don't consider whether the individual mutations that cause cell cycle dysregulation can affect cancer's eventual response to treatment or its ability to spread," said Haricharan.
By connecting the specific type of cell cycle dysregulation that triggers cancer with the outcome of the disease many years after diagnosis, the research team proposes an entirely new paradigm for thinking about and studying all types of cancer.
"This is a radical shift in how we look at cancer, which could have implications well beyond breast cancer," added Haricharan.
To begin to test this idea, the researchers analyzed the effect of cell cycle mutations on patient outcomes in other types of cancer. In a final twist, they observed that across many cancer types, the mode of cell cycle dysregulation is significant for cancer in women, but less so for cancer in men. This suggests that the influence of cell-cycle dysregulation could depend on sex as well as age. "These findings emphasize why it is important to study cancer in the context of the life history of the patient," said Haricharan, adding, "Too often, cancer research is focused narrowly on cells in a petri dish, forgetting the whole, complex host system in which these cells transform and grow." —ANI
