Asst. Prof. \u00d6zg\u00fcr \u015eahin, a faculty member in the Department of Molecular Biology and Genetics (MBG) and UNAM, and his team have recently published their work in two leading journals in the field of cancer: the Nature Publishing Group journal Oncogene, and the American Association for Cancer Research (AACR) journal Clinical Cancer Research. In two preclinical studies, Dr. \u015eahin and his team identified genes responsible for drug resistance in two subtypes of breast cancer. They showed that targeting the proteins synthesized by these genes reverses resistance and causes tumor shrinkage in mouse models of the disease. Asst. Prof. Can Alkan, a faculty member in the Department of Computer Engineering, contributed to the first study, while Asst. Prof. \u00c7a\u011flar \u00c7eki\u00e7, an MBG and UNAM faculty member, contributed to the second.<\/p>\n
Development of drug resistance is one of the major obstacles to effective cancer treatment, and one of the leading causes of cancer-related deaths. Cancer cells develop resistance to a variety of anticancer therapeutics, including chemotherapy and targeted therapy agents. Identifying the molecular mechanisms of drug resistance and thereby increasing the effectiveness of drugs by targeting the identified molecules is crucial and will have a huge impact on improving patient outcome.<\/p>\n
In the first project, which was funded by T\u00dcB\u0130TAK, Dr. \u015eahin and his team identified the molecular mechanisms of resistance against the drug trastuzumab-emtansine
\n(T-DM1). T-DM1 was approved by the US Food and Drug Administration (FDA) in 2013 and since then has been used in metastatic HER2-positive breast cancer patients, who constitute around 20 percent of all breast cancer patients. This study identified the protein polo-like kinase 1 (PLK1) as being upregulated in T-DM1 resistance and demonstrated that targeting PLK1 with a small- molecule inhibitor, volasertib, increases drug sensitivity.<\/p>\n
In the second project, which was funded by the European Molecular Biology Organization (EMBO), the researchers demonstrated that hyperactivation of the enzyme phosphodiesterase 4D, which is produced by the PDE4D gene, is responsible for resistance to tamoxifen. Tamoxifen has long been used to treat ER-positive breast cancer, which constitutes around 70 percent of all breast cancer cases. Targeting phosphodiesterase 4D with dipyridamole or aspirin enhanced tamoxifen response in cell-line and mouse models of tamoxifen-resistant ER-positive breast cancer. Interestingly, this study demonstrated that aspirin, a drug that has been used for over a century for various purposes, can overcome tamoxifen resistance and decrease tumor burden in ER-positive breast cancer.<\/p>\n
These two preclinical studies have identified two important genes mediating drug resistance and paved the way toward testing drugs that are either being tested in clinical trials for other cancers (e.g., volasertib) or already approved by the FDA (e.g., aspirin) in clinics for treatment-refractory breast cancer subtypes in the near future.<\/p>\n","protected":false},"excerpt":{"rendered":"
Asst. Prof. \u00d6zg\u00fcr \u015eahin, a faculty member in the Department of Molecular Biology and Genetics (MBG) and UNAM, and his team have recently published their work in two leading journals […]<\/p>\n","protected":false},"author":1,"featured_media":2992,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"inline_featured_image":false,"footnotes":""},"categories":[36],"tags":[],"class_list":["post-2991","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news-2018"],"yoast_head":"\n