Tumor Marker Overcomes Endocrine Treatment-resistant Breast Cancer

For decades, these tumors have been treated with anti-estrogen (endocrine) therapies to lower estrogen levels and help slow the cancer’s growth.

“We know there is a subset of patients who are initially diagnosed with ER-positive, HER2-negative breast tumors, but their tumors convert to HER2-positive after they receive endocrine therapy,” says Svasti Haricharan, Ph.D., assistant professor in the Aging, Cancer and Immuno-oncology Program at Sanford Burnham Prebys and senior author of the study. “Unfortunately, this unleashes the detrimental effects of HER2, and patients become resistant to endocrine therapy—resulting in relapse, metastasis and death.”

With conventional endocrine therapy being unhelpful for these patients, Haricharan’s team examined how two genes, MLH1 and PMS2, affect HER2 activity. These genes are part of a biological system to “fix” DNA errors—but they also play a critical role in suppressing HER2. When these genes are turned off, HER2 becomes activated as soon as patients receive standard care endocrine therapy.

“Fortunately, there are tests for MLH1 and PMS2 activity that are now done routinely for colorectal and endometrial cancers,” says Nindo Punturi, a research assistant in the Haricharan lab and first author of the paper. “If we were to transition these tests to newly diagnosed cases of breast cancer, we could identify patients who may benefit from early HER2-targeted treatment—essentially shutting the door to HER2 activity before it gets started.”

The National Cancer Institute (NCI) estimates that 281,550 women in the U.S. will be diagnosed with breast cancer in 2021, and 43,600 women will eventually die from the disease. Some women whose MLH1 and PMS2 gene expression is low or absent may have an even greater risk of death.

“Our research efforts are all about getting the right treatments to the right people as soon as possible,” says Haricharan. “With so many excellent drugs at our disposal to treat breast cancer—including those that target HER2—it’s more a matter of selecting the available, appropriate drugs than searching for new ones. This research effort is an important step in that direction.”

Additional study authors include Nindo B. Punturi, Sinem Seker and Aloran Mazumder at Sanford Burnham Prebys; Vaishnavi Devarakonda, Rashi Kalra, Ching-Hui Chen, Matthew J. Ellis and Shyam M. Kavuri at Baylor College of Medicine in Houston; and Shunqiang Li and Tina Primeau at Washington University in St. Louis.

Source: Newswise