C1orf106, an innate immunity activator, is amplified in breast cancer and is required for basal-like/luminal progenitor fate decision

Sci China Life Sci. 2019 Sep;62(9):1229-1242. doi: 10.1007/s11427-019-9570-y. Epub 2019 Aug 1.

Abstract

Basal-like breast cancer with a luminal progenitor gene expression profile is an aggressive subtype of breast cancer with a poorer prognosis compared with other subtypes. However, genes that specifically promote basal-like breast cancer development remain largely unknown. Here, we report that a novel gene C1orf106 plays an important role in maintaining the feature of basal-like/luminal progenitors. C1orf106 is frequently amplified and overexpressed in basal-like breast cancer and is associated with a poor outcome in patients. In human TCGA database, C1orf106 expression was correlated with upregulation of ELF5 and downregulation of GATA3, two transcription factors that regulate mammary gland stem cell fate. Enhanced expression of C1orf106 promotes tumor progression and expression of basal-like/luminal progenitor marker ELF5; depletion of C1orf106 suppresses tumorigenesis and expression of basal-like/luminal progenitor marker GATA3. These findings suggest that C1orf106 maintains the basal-like/luminal progenitor character through balancing the expression of ELF5 and GATA3. Taken together, we demonstrated that C1orf106 is an important regulator for basal-like/luminal progenitors and targeting C1orf106 is of therapeutic value for breast cancer.

Keywords: C1orf106; ELF5; GATA3; basal-like; breast cancer; luminal progenitor.

MeSH terms

  • Breast Neoplasms / genetics*
  • Breast Neoplasms / metabolism
  • Carcinogenesis / genetics
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Proliferation
  • Cell Transformation, Neoplastic / genetics
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Databases, Nucleic Acid
  • Female
  • GATA3 Transcription Factor / genetics*
  • GATA3 Transcription Factor / metabolism
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunity, Innate / genetics*
  • Immunity, Innate / physiology
  • Neoplasms, Basal Cell / genetics*
  • Neoplasms, Basal Cell / pathology
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • Carrier Proteins
  • DNA-Binding Proteins
  • ELF5 protein, human
  • GATA3 Transcription Factor
  • GATA3 protein, human
  • INAVA protein, human
  • Transcription Factors