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CK20 Expression Enhances the Invasiveness of Tamoxifen-resistant MCF-7 Cells

Cited 8 time in Web of Science Cited 9 time in Scopus
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

Issue Date
2012-04
Publisher
International Institute of Anticancer Research
Citation
Anticancer Research, Vol.32 No.4, pp.1221-1228
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 gamma (PPAR gamma). Our findings suggest that PPAR gamma-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.
ISSN
0250-7005
URI
https://hdl.handle.net/10371/191566
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  • College of Medicine
  • Department of Medicine
Research Area 3D drug screening, Cancer Organoid, Precision Oncologuy

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