New findings may enhance PARP inhibitors therapy in breast cancer
Study may hold promise for other cancers that overexpress c-MET
MD Anderson News Release January 18, 2016
Findings from a new study reveal that PARP inhibitors, an emerging class of drugs being studied in cancer clinical trials, may be enhanced by combining them with inhibitors targeting an oncogene known as c-MET which is overexpressed in many cancers.
The findings resulting from in vitro and mouse model studies were published in today’s online issue of Nature Medicine. Study lead investigator Mien-Chie Hung, Ph.D., chair of Molecular and Cellular Oncology at The University of Texas MD Anderson Cancer Center, believes the study results may hold promise for future treatment of breast cancer and possibly other cancers.
“These findings may predict tumor resistance to PARP inhibitors and suggest that treatment with a combination of c-MET and PARP inhibitors may benefit patients bearing tumors with high c-MET expression who do not respond to PARP inhibition alone,” said Hung.
While PARP inhibitors are still in the clinical trial phases for breast cancer, the FDA recently approved the PARP inhibitor olaparib for treatment of ovarian cancer with mutations in breast cancer genes known as BRCA.
“BRCA1 and BRCA2 play essential roles in repairing DNA double strand breaks and a deficiency of BRCA proteins sensitizes cancer cells to PARP inhibition,” said Hung. “Combining c-MET and PARP1 inhibitors synergized to suppress growth of breast cancer cells. Similar synergistic effects were also observed in a lung cancer mouse model.”
Hung’s team discovered that c-MET associates with and phosphorylates PARP1, which increases its enzymatic activity. This process essentially renders cancer cells resistant to PARP inhibition. By blocking c-MET’s cancer-friendly interaction with PARP, cancer cells lose this resistance to the therapy.
“Our study findings raise the interesting possibility that cancer patients with tumors that overexpress c-MET may benefit from this combination therapy regardless of cancer type,” said Hung.
MD Anderson participants in the study included Yi Du, Ph.D., Hirohito Yamaguchi, D.V.M., Ph.D., Yongkun Wei, Ph.D., Jennifer Hsu, Ph.D., Yi-Hsin Hsu, Ph.D., Wan-Chi Lin, Ph.D., Wen-Hsuan Yu, Mei-Kuang Chen, Katsuya Nakai, M.D., Ph.D., Ming-Chuan Hsu, Ph.D., Ye Sun and Chun-Te Chen, Ph.D., all of Molecular and Cellular Oncology; Paul Leonard, Ph.D., and Gilbert Lee IV, Genomic Medicine; Philip Jones, Ph.D., Institute for Applied Cancer Science; Yun Wu, M.D., Ph.D., Pathology; and Gabriel Hortobagyi, M.D., Breast Medical Oncology.
Other participating institutions included China Medical University, Taichung, Taiwan; The University of Texas Graduate School of Biomedical Sciences, Houston; Academia Sinica, Taipei; Mackay Memorial Hospital, Taipei; McGill University, Montreal; and Asia University, Taichung, Taiwan.
The study was funded by the National Institutes of Health (CA109311, CA099031 and CA16672), the Susan G. Komen For the Cure (SAC100016), Breast Cancer Research Foundation, Patel Memorial Breast Cancer Endowment Fund, The University of Texas MD Anderson-China Medical University and Hospital Sister Institution Fund; Ministry of Science and Technology, International Research-Intensive Centers of Excellence in Taiwan (I-RiCE), MOST (104-2911-I-002-302), Ministry of Health and Welfare, China Medical University Hospital, and the Ting Tsung and Wei Fong Chao Research Fund.