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조수지 이재면(미생물학교실) Oncotarget
등록일 : 2017-11-13 오후 3:18:00       조회 : 52
첨   부 :
제1저자 조수지(미생물학교실, BK21 졸) 박필구(미생물학교실)
교신저자 동승명(NCC) 이재면(미생물학교실, BK21)

Oncotarget. 2017 Aug 12ɖ(45):78781-78795. doi: 10.18632/oncotarget.20227. eCollection 2017 Oct 3.

Cellular inhibitor of apoptosis protein 2 promotes the epithelial-mesenchymal transition in triple-negative breast cancer cells through activation of the AKT signaling pathway.

Jo SJ1,2, Park PG1, Cha HR1, Ahn SG3, Kim MJ1, Kim H1,2, Koo JS4, Jeong J3, Park JH1, Dong SM5,6, Lee JM1,2.

Author information

1Department of Microbiology and Immunology, Yonsei University College of Medicine, Seoul, Republic of Korea.2BK21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, Republic of Korea.3Breast Cancer Center, Department of Surgery, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.4Department of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.5Research Institute, National Cancer Center, Goyang, Republic of Korea.6IMK Bio-Convergence R&D Center, International Vaccine Institute, Seoul, Republic of Korea.

Triple-negative breast cancer (TNBC) represents approximately 10-17% of all breast cancers, and patients with TNBC show a poorer short-term prognosis than patients with other types of breast cancer. TNBCs also have a higher tendency for early distant metastasis and cancer recurrence due to induction of the epithelial-mesenchymal transition (EMT). Several recent reports have suggested that inhibitor of apoptosis (IAP) proteins function as regulators of the EMT. However, the roles of these proteins in TNBC are not clear. Accordingly, we investigated the roles of cIAP2 in TNBC. Among eight IAP genes, only cIAP2 was upregulated in TNBC cells compared with that in other breast cancer subtypes. Analysis of TMAs revealed that expression of cIAP2 was upregulated in TNBCs. In vitro studies showed that cIAP2 was highly expressed in TNBC cells compared with that in other types of breast cancer cells. Furthermore, silencing of cIAP2 in TNBC cells induced mesenchymal-epithelial transition (MET)-like processes and subsequently suppressed the migratory ability and invasion capacity of the cells by regulation of Snail through the AKT signaling pathway. In contrast, ectopic expression of cIAP2 in luminal-type breast cancer cells induced activation of the AKT signaling pathway. These results collectively indicated that cIAP2 regulated the EMT in TNBC via activation of the AKT signaling pathway, contributing to metastasis in TNBC. Our study proposes a novel mechanism through which cIAP2 regulates the EMT involving AKT signaling in TNBC cells. We suggest that cIAP2 may be an attractive candidate molecule for the development of targeted therapeutics in the future.
박채규(의생명과학부) J Invest Dermatol 2017-11-17
김재우(생화학-분자생물학교실) Sci Rep 2017-11-06