Establishment and characterization of a prostatic small-cell carcinoma cell line (PSK-1) derived from a patient with Klinefelter syndrome

Prostate. 2000 Mar 1;42(4):287-94. doi: 10.1002/(sici)1097-0045(20000301)42:4<287::aid-pros6>3.0.co;2-f.

Abstract

Background: Prostatic small-cell carcinoma (SMCC) is an extremely aggressive, rarely occurring tumor, and there has been no previous report of prostatic SMCC in association with Klinefelter syndrome. This study reports on the first such case and the establishment of the first cell line of SMCC from this tumor.

Methods: Prostatic SMCC tissue was derived from a 29-year-old man with Klinefelter syndrome. Characteristics of the culture tumor cells were evaluated with cell growth in vitro, neuron-specific enolase (NSE) secretion ability, tumorigenicity in nude mice, chemosensitivity to anticancer drugs, and karyotypic analysis.

Results: A culture cell line (PSK-1) was successfully established from prostatic SMCC with Klinefelter syndrome. PSK-1 cells had a polygonal epithelioid morphology and demonstrated loss of contact inhibition. These cells secreted NSE into the culture supernatant. Tumors produced in nude mice were histologically similar to the original SMCC. In a chemosensitivity test, PSK-1 cells were found to be sensitive in vitro to cisplatin, etoposide, and doxorubicin, but resistant to dacarbazine and 5-fluorouracil. Cytogenetic analysis showed that the PSK-1 cells at passage 35 revealed 76-84 chromosomes, with a mode of 82 chromosomes.

Conclusions: PSK-1 cells could represent some properties of the original tumor cells, and could be used in studies on the etiology and treatment of this disease.

MeSH terms

  • Adult
  • Animals
  • Antineoplastic Agents / pharmacology
  • Carcinoma, Small Cell / complications
  • Carcinoma, Small Cell / enzymology
  • Carcinoma, Small Cell / genetics
  • Carcinoma, Small Cell / pathology*
  • Cell Division
  • Cisplatin / pharmacology
  • Dacarbazine / pharmacology
  • Doxorubicin / pharmacology
  • Etoposide / pharmacology
  • Fluorouracil / pharmacology
  • Humans
  • Karyotyping
  • Klinefelter Syndrome / complications*
  • Klinefelter Syndrome / genetics
  • Klinefelter Syndrome / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasm Transplantation
  • Phosphopyruvate Hydratase / metabolism
  • Prostatic Neoplasms / complications
  • Prostatic Neoplasms / enzymology
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / pathology*
  • Tumor Cells, Cultured*

Substances

  • Antineoplastic Agents
  • Etoposide
  • Dacarbazine
  • Doxorubicin
  • Phosphopyruvate Hydratase
  • Cisplatin
  • Fluorouracil