CK20 expression enhances the invasiveness of tamoxifen-resistant MCF-7 cells |
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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 |
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Affiliation: | Department of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea. |
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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. |
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