Complement proteins C7 and CFH control the stemness of liver cancer cells via LSF-1

Cancer Lett. 2016 Mar 1;372(1):24-35. doi: 10.1016/j.canlet.2015.12.005. Epub 2015 Dec 23.

Abstract

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.

Keywords: CFH; Complement protein C7; HCC; LSF-1; Liver tumor-initiating cell; Stemness factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Cell Differentiation*
  • Cell Line, Tumor
  • Cell Proliferation*
  • Complement C7 / genetics
  • Complement C7 / immunology
  • Complement C7 / metabolism*
  • Complement Factor H / genetics
  • Complement Factor H / immunology
  • Complement Factor H / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Female
  • Gene Expression Regulation, Neoplastic
  • Heterografts
  • Humans
  • Immunity, Innate
  • Liver Neoplasms / genetics
  • Liver Neoplasms / immunology
  • Liver Neoplasms / metabolism*
  • Liver Neoplasms / pathology
  • Male
  • Mice, Inbred NOD
  • Mice, SCID
  • Middle Aged
  • Neoplastic Stem Cells / immunology
  • Neoplastic Stem Cells / metabolism*
  • Neoplastic Stem Cells / pathology
  • Phenotype
  • RNA Interference
  • Signal Transduction
  • Spheroids, Cellular
  • Time Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transfection
  • Tumor Burden
  • Tumor Cells, Cultured

Substances

  • CFH protein, human
  • Complement C7
  • DNA-Binding Proteins
  • TFCP2 protein, human
  • Transcription Factors
  • Complement Factor H