Clonal analysis revealed functional heterogeneity in cancer stem-like cell phenotypes in uterine endometrioid adenocarcinoma

Exp Mol Pathol. 2019 Feb:106:78-88. doi: 10.1016/j.yexmp.2018.11.013. Epub 2018 Nov 30.

Abstract

Uterine endometrial carcinoma is one of the common cancers in females. Cancer stem-like cells (CSCs)/cancer-initiating cells (CICs) are a small subpopulation of cancer cells that are tumorigenic and are resistant to treatments, thus they are focused as treatment targets. However, the heterogeneity of CSCs/CICs is still elusive, and we therefore analyzed CSCs/CICs at the clonal level. We previously established sphere-cultured CSCs/CICs from primary human uterine endometrial carcinoma, and we isolated several clones from CSCs/CICs in this study. Interestingly, we established two types of clones based on the growth pattern. The clones were termed sphere clones (S clones) and leukemia-like clones (LL clones). Functional analysis revealed that S clones are resistant to chemotherapy, whereas LL clones are sensitive to chemotherapy. On the other hand, S clones are less tumorigenic, while LL clones are highly tumorigenic. Transcriptome analysis using serial analysis of gene expression sequencing (SAGE-Seq) revealed distinctive gene expression profiles in S clone cells and LL clone cells. The results indicate that CSCs/CICs are composed of functionally heterogenic subpopulations including highly tumorigenic clones and treatment-resistant clones and that the characteristics of CSCs/CICs might be determined by the characteristics of different clones that compose CSCs/CICs.

Keywords: Cancer stem cell; Chemo-resistance; Endometrial carcinoma; SAGE-Seq; Tumorigenicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carboplatin / pharmacology
  • Carcinoma, Endometrioid / genetics
  • Carcinoma, Endometrioid / pathology*
  • Clone Cells / pathology
  • Culture Media
  • DNA, Neoplasm / genetics
  • Endometrial Neoplasms / genetics
  • Endometrial Neoplasms / pathology*
  • Female
  • Gene Expression Regulation, Neoplastic
  • Heterografts
  • Humans
  • Mice
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / pathology*
  • Paclitaxel / pharmacology
  • Phenotype
  • Sequence Analysis, DNA
  • Serum
  • Spheroids, Cellular
  • Tumor Cells, Cultured

Substances

  • Culture Media
  • DNA, Neoplasm
  • Carboplatin
  • Paclitaxel