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Complement proteins C7 and CFH control the stemness of liver cancer cells via LSF-1.
Seol, Hyang Sook; Lee, Sang Eun; Song, Joon Seon; Rhee, Je-Keun; Singh, Shree Ram; Chang, Suhwan; Jang, Se Jin.
Afiliación
  • Seol HS; Asan Institute for Life Science, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Lee SE; Asan Institute for Life Science, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Song JS; Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Rhee JK; Department of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Singh SR; Basic Research Laboratory, Stem Cell Regulation and Animal Aging Section, Center for Cancer Research, National Cancer Institute, Frederick, MD, USA.
  • Chang S; Department of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea. Electronic address: suhwan.chang@amc.seoul.kr.
  • Jang SJ; Asan Institute for Life Science, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea; Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea. Electronic address: jangsejin@amc.seoul.kr.
Cancer Lett ; 372(1): 24-35, 2016 Mar 01.
Article en En | MEDLINE | ID: mdl-26723877
Tumor-initiating cells are important for the formation and maintenance of tumor bulks in various tumors. To identify surface markers of liver tumor-initiating cells, we performed primary tumorsphere culture and analyzed the expression of cluster of differentiation (CD) antigen genes using NanoString. Interestingly, we found significant upregulation of the complement proteins (p = 1.60 × 10(-18)), including C7 and CFH. Further studies revealed that C7 and CFH are required to maintain stemness in liver cancer cells. Knockdown of C7 and CFH expression abrogated tumorsphere formation and induced differentiation, whereas overexpression stimulated stemness factor expression as well as in vivo cell growth. Mechanistically, by studying C7 and CFH-dependent LSF-1 expression and its direct role on stemness factor transcription, we found that LSF-1 is involved in this regulation. Taken together, our data demonstrate the unprecedented role of complement proteins on the maintenance of stemness in liver tumor-initiating cells.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Células Madre Neoplásicas / Complemento C7 / Diferenciación Celular / Proliferación Celular / Proteínas de Unión al ADN / Neoplasias Hepáticas Tipo de estudio: Prognostic_studies Idioma: En Revista: Cancer Lett Año: 2016 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Células Madre Neoplásicas / Complemento C7 / Diferenciación Celular / Proliferación Celular / Proteínas de Unión al ADN / Neoplasias Hepáticas Tipo de estudio: Prognostic_studies Idioma: En Revista: Cancer Lett Año: 2016 Tipo del documento: Article