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CK20 expression enhances the invasiveness of tamoxifen-resistant MCF-7 cells
Authors:Min Yun Sook  Yi Eun Hee  Lee Jin Koo  Choi Ji Won  Sim Ji Hyun  Kang Jae-Seung  Kim Yong-Nyun  Juhnn Yong-Sung  Kim Hang-Rae  Ye Sang-Kyu
Affiliation:Department of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Abstract:
Cytokeratin 20 (CK20) is an intermediate filament that is known to be a prognostic marker in several types of cancer. However, little is known about CK20 expression and tumor metastasis in tamoxifen-resistant MCF-7 (TRM-7) breast cancer cells. TRM-7 cells overexpress CK20, resulting in enhanced invasiveness in vitro. CK20 silencing reduced the invasiveness of TRM-7 cells. Moreover, CK20 expression in MCF-7 cells was regulated by peroxisome proliferator-activated receptor γ (PPARγ). Our findings suggest that PPARγ-dependent CK20 expression enhances the metastatic potential of MCF-7 breast cancer cells and may be a potential therapeutic target in tamoxifen-resistant breast cancer.
Keywords:
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