| Literature DB >> 33364954 |
Zhen Li1, Wei Zou2, Ji Zhang1, Yunjiao Zhang3, Qi Xu4, Siyuan Li5, Ceshi Chen5,6,7,8.
Abstract
As a new-generation CDK inhibitor, a CDK4/6 inhibitor combined with endocrine therapy has been successful in the treatment of advanced estrogen receptor-positive (ER+) breast cancer. Although there has been overall progress in the treatment of cancer, drug resistance is an emerging cause for breast cancer-related death. Overcoming CDK4/6 resistance is an urgent problem. Overactivation of the cyclin-CDK-Rb axis related to uncontrolled cell proliferation is the main cause of CDK4/6 inhibitor resistance; however, the underlying mechanisms need to be clarified further. We review various resistance mechanisms of CDK4/6 inhibitors in luminal breast cancer. The cell signaling pathways involved in therapy resistance are divided into two groups: upstream response mechanisms and downstream bypass mechanisms. Finally, we discuss possible strategies to overcome CDK4/6 inhibitor resistance and identify novel resistance targets for future clinical application.Entities:
Keywords: CDK4/6 inhibitor; downstream bypass signaling; endocrine resistance; luminal breast cancer; upstream response signaling
Year: 2020 PMID: 33364954 PMCID: PMC7751736 DOI: 10.3389/fphar.2020.580251
Source DB: PubMed Journal: Front Pharmacol ISSN: 1663-9812 Impact factor: 5.810