GT198 Expression Defines Mutant Tumor Stroma in Human Breast Cancer

Zheqiong Yang, Min Peng, Liang Cheng, Kimya Jones, Nita Jane Maihle, Nahid F Mivechi, Lan Ko

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

Human breast cancer precursor cells remain to be elucidated. Using breast cancer gene product GT198 (PSMC3IP; alias TBPIP or Hop2) as a unique marker, we revealed the cellular identities of GT198 mutant cells in human breast tumor stroma. GT198 is a steroid hormone receptor coactivator and a crucial factor in DNA repair. Germline mutations in GT198 are present in breast and ovarian cancer families. Somatic mutations in GT198 are present in ovarian tumor stromal cells. Herein, we show that human breast tumor stromal cells carry GT198 somatic mutations and express cytoplasmic GT198 protein. GT198+ stromal cells share vascular smooth muscle cell origin, including myoepithelial cells, adipocytes, capillary pericytes, and stromal fibroblasts. Frequent GT198 mutations are associated with GT198+ tumor stroma but not with GT198- tumor cells. GT198+ progenitor cells are mostly capillary pericytes. When tested in cultured cells, mutant GT198 induces vascular endothelial growth factor promoter, and potentially promotes angiogenesis and adipogenesis. Our results suggest that multiple lineages of breast tumor stromal cells are mutated in GT198. These findings imply the presence of mutant progenitors, whereas their descendants, carrying the same GT198 mutations, are collectively responsible for forming breast tumor microenvironment. GT198 expression is, therefore, a specific marker of mutant breast tumor stroma and has the potential to facilitate diagnosis and targeted treatment of human breast cancer.

Original languageEnglish (US)
Pages (from-to)1340-1350
Number of pages11
JournalAmerican Journal of Pathology
Volume186
Issue number5
DOIs
StatePublished - May 1 2016

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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