Masafumi Iida, Daichi Toyosawa, Misato Nakamura, Kouki Tsuboi, Emi Tokuda, Toshifumi Niwa, Takanori Ishida, Shin-Ichi Hayashi
Breast cancer (Tokyo, Japan) 2020 SepCyclin-dependent kinase (CDK) 4/6 inhibitors represent a significant advancement in the treatment of estrogen receptor (ER)-positive human epidermal growth factor receptor 2-negative advanced breast cancer. However, mechanisms of alterations after acquired resistance to CDK4/6 inhibitors and the optimal treatment options are still not established. Abemaciclib-resistant cell lines were established from the models of estrogen deprivation-resistant cell lines which retained ER expression and activated ER function derived from MCF-7 breast cancer cell lines. Ribocilib-resistant cell lines were established in the same method as previously reported. Both abemaciclib- and ribociclib-resistant cell lines showed decreased ER expression. ER transcriptional activity was maintained in these cell lines; however, the sensitivity to 4-hydroxytamoxifen and fulvestrant was almost completely lost. These cell lines did not exhibit any ERα gene mutation. Abemaciclib-resistant cell lines demonstrated low sensitivity to other CDK4/6 inhibitors; sensitivities to PI3K inhibitor, mTOR inhibitor, and chemotherapeutic drugs were maintained. Dependence on ER signaling appears to decrease after the development of acquired resistance to CDK4/6 inhibitors. Further, CDK4/6 inhibitor-resistant cells acquired cross-resistance to other CDK4/6 inhibitors, PI3K/Akt/mTOR inhibitor therapy and chemotherapeutic drugs might serve as optimal treatment options for such breast cancers.
Masafumi Iida, Daichi Toyosawa, Misato Nakamura, Kouki Tsuboi, Emi Tokuda, Toshifumi Niwa, Takanori Ishida, Shin-Ichi Hayashi. Decreased ER dependency after acquired resistance to CDK4/6 inhibitors. Breast cancer (Tokyo, Japan). 2020 Sep;27(5):963-972
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PMID: 32297248
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