Establishment and characterization of a prostate cancer cell line from a prostatectomy specimen for the study of cellular interaction

Ruoxiang Wang, Gina C.Y. Chu, Xudong Wang, Jason B. Wu, Peizhen Hu, Asha S. Multani, Sen Pathak, Haiyen E. Zhau, Leland W.K. Chung

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Though human prostate cancer (PCa) heterogeneity can best be studied using multiple cell types isolated from clinical specimens, the difficulty of establishing cell lines from clinical tumors has hampered this approach. In this proof-of-concept study, we established a human PCa cell line from a prostatectomy surgical specimen without the need for retroviral transduction. In a previous report, we characterized the stromal cells derived from PCa specimens. Here, we characterized the epithelial cells isolated from the same tumors. Compared to the ease of establishing prostate stromal cell lines, prostatic epithelial cell lines are challenging. From three matched pairs of normal and tumor tissues, we established one new PCa cell line, HPE-15. We confirmed the origin of HPE-15 cells by short tandem repeat microsatellite polymorphism analysis. HPE-15 cells are androgen-insensitive and express marginal androgen receptor, prostate-specific antigen and prostate-specific membrane antigen proteins. HPE-15 expresses luminal epithelial markers of E-cadherin and cytokeratin 18, basal cell markers of cytokeratin 5 and p63 and neuroendocrine marker of chromogranin A. Interestingly, HPE-15 Cells exhibited no tumorigenicity in different strains of immune-deficient mice but can become tumorigenic through interaction with aggressive cancer cell types. HPE-15 cells can thus serve as an experimental model for the study of PCa progression, metastasis and tumor cell dormancy.

Original languageEnglish (US)
Pages (from-to)2249-2259
Number of pages11
JournalInternational journal of cancer
Volume145
Issue number8
DOIs
StatePublished - Oct 15 2019

Keywords

  • and cell–cell interaction
  • cell line
  • prostate cancer
  • transit amplifying

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

MD Anderson CCSG core facilities

  • Cytogenetics and Cell Authentication Core

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