Japanese researchers have revealed mechanism how breast cancer evolves as entire process
The team from the Kyoto University showed the mechanism by which breast cancer is formed in the cells of the mammalian epithelium, whose main function is to secrete milk.
Tokyo: Japanese researchers have revealed the mechanism how breast cancer evolves as the entire process — from the early stages of cell mutations starting in puberty to their manifestations as breast cancer in later years — has remained shrouded in mystery.
The team from the Kyoto University showed the mechanism by which breast cancer is formed in the cells of the mammalian epithelium, whose main function is to secrete milk.
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The findings are published in the journal Nature. According to the team’s first analysis, approximately 20 mutations accumulate annually in each epithelial cell until menopause. After menopause, however, the mutation rate significantly decreases.
“Additionally, our results suggest that oestrogen influences mutation accumulation in mammary epithelium, which correlates with our discovery of decreased accumulation after childbirth,” said Seishi Ogawa from the varsity’s Graduate School of Medicine.
As 70 per cent of breast cancers are understood to be oestrogen-sensitive, Ogawa’s team may shed light on oestrogen’s role in the initiation of breast cancer. Further investigation of the genetic relationship between breast cancer, its surrounding lesions, and normal epithelial cells led to mapping breast cancer’s translocation-positive expansion.
During this expansion process, cells of multiple origins that would subsequently develop breast cancer manifested themselves at the average age of 30. Previous studies have focused on driver mutations — the genetic changes in cells that are already cancerous — leading to abnormal growth.
But these findings only paint a partial picture of the process and do not reveal the timing and order of driver mutations or cancer formation. “Normal-looking tissues may already contain numerous populations of non-cancer cells — or clones — that have acquired mutations in cancer-related genes,” said co-author author Tomomi Nishimura from the Graduate School of Medicine at the varsity.
After examining the similarities and differences in the mutations of both cancer and non-cancer lesions originating from the clones, the team reconstructed an evolutionary tree to visualise the unique pattern of cancer evolution. “Our study brings us closer to exposing the clinical profile of oestrogen-sensitive breast cancer, particularly in pre-menopausal women, potentially aiding cancer risk monitoring and prevention,” Ogawa said.
