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// Zhen Li 1, 2, 3, * , Jian Dong 4, * , Tianning Zou 5 , Chengzhi Du 2 , Siyuan Li 2 , Ceshi Chen 2 , Rong Liu 2 , Kunhua Wang 1, 3 1 Department of Gastrointestinal and Hernia Surgery, Institute of Gastroenterology, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, China 2 Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Kunming, Yunnan 650223, China 3 Kunming Digestive Disease Treatment Engineering Technology Center, Kunming, Yunnan 650032, China 4 Department of Oncology, Yunnan Tumor Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650118, China 5 Department of Breast Surgery, Yunnan Tumor Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650118, China * These authors have contributed equally to this work Correspondence to: Kunhua Wang, email: wkh1963@yeah.net Rong Liu, email: liurong@mail.kiz.ac.cn Ceshi Chen, email: chenc@mail.kiz.ac.cn Keywords: Dex, GR, KLF5, TNBC, drug resistance Received: July 18, 2016 Accepted: November 22, 2016 Published: December 24, 2016 ABSTRACT Purpose : Dexamethasone (Dex), a glucocorticoid (GC), is used as a pretreatment drug in cancer patients undergoing chemotherapy. Dex functions by binding to the glucocorticoid receptor (GR) to prevent allergic reactions and severe chemotherapeutic side effects such as nausea and vomiting. However, the mechanisms by which Dex causes chemoresistance remain unknown. Methods : We used docetaxel and cisplatin to treat triple-negative breast cancer (TNBC) cells with or without Dex and assessed cell proliferation using a sulforhodamine B colorimetric (SRB) assay. Additionally, Western blotting was employed to measure Krüppel-like factor 5 (KLF5), GR and several apoptosis-related proteins. To determine how the GR regulates KLF5, we used qRT-PCR, luciferase reporter assays and ChIP assays. Finally, we detected the involvement of Dex in TNBC chemotherapeutic resistance using HCC1806 xenograft model in vivo . Results: In this study, we demonstrated that Dex induces docetaxel and cisplatin resistance in TNBC cells in vitro and in vivo . Dex up-regulates pro-survival transcription factor KLF5 expression at both mRNA and protein levels dependent on GR. Importantly, Dex failed to promote cancer cell survival and tumor growth when KLF5 induction was blocked. Conclusions : We conclude that KLF5 is a Dex-induced gene that contributes to Dex-mediated drug chemoresistance, providing a potential novel target for TNBC treatment.
Li et al. (Sat,) studied this question.