Re-expression of p16(INK4a) in mesothelioma cells results in cell cycle arrest, cell death, tumor suppression and tumor regression

Sandra P. Frizelle, Jon Grim, Joan Zhou, Pankaj Gupta, David T. Curiel, Joseph Geradts, Robert A. Kratzke

Research output: Contribution to journalArticlepeer-review

107 Scopus citations

Abstract

Absence of expression of the p16(INK4a) gene product is commonly observed in mesothelioma tumors and cell lines, while mild-type pRB expression is maintained. We have examined the biologic and potential therapeutic role of re-expressing p16(INK4a) gene product in mesothelioma cells and tumors. Following transduction with a p16(INK4a) expressing adenovirus (Adp16), over-expression of p16(INK4a) in mesothelioma cells resulted in cell cycle arrest, inhibition of pRB phosphorylation, diminished cell growth, and eventual death of the transduced cells. Expression of p16(INK4a) protein was accompanied by decreased expression of pRB as detected by immunoblot and immunohistochemistry. Experiments in mesothelioma xenografts demonstrated inhibition of tumor formation, tumor growth arrest and diminished tumor size and spread, p16(INK4a) gene product expression was also demonstrated in intraperitoneal xenografts of human mesothelioma cells. These results demonstrate that p16(INK4a) gene transfer may play a therapeutic role in the treatment of mesothelioma.

Original languageEnglish
Pages (from-to)3087-3095
Number of pages9
JournalOncogene
Volume16
Issue number24
DOIs
StatePublished - Jun 18 1998
Externally publishedYes

Keywords

  • Mesothelioma
  • Tumor suppressor
  • p16(INK4a)

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