Involvement of PPARs in Cell Proliferation and Apoptosis in Human Colon Cancer Specimens and in Normal and Cancer Cell Lines
Author(s) -
Germana Martinasso,
Manuela Oraldi,
Antonella Trombetta,
M. Maggiora,
Oscar Bertetto,
Rosa Angela Canuto,
Giuliana Muzio
Publication year - 2007
Publication title -
ppar research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 49
eISSN - 1687-4765
pISSN - 1687-4757
DOI - 10.1155/2007/93416
Subject(s) - in vivo , algorithm , apoptosis , colorectal cancer , cancer , cell growth , medicine , artificial intelligence , biology , computer science , biochemistry , genetics
PPAR involvement in cell growth was investigated “in vivo” and “in vitro” and was correlated with cell proliferation and apoptotic death. “In vivo” PPAR γ and α were evaluated in colon cancer specimens and adjacent nonneoplastic colonic mucosa. PPAR γ increased in most cancer specimens versus mucosa, with a decrease in c-Myc and in PCNA proteins, suggesting that colon cancer growth is due to increased cell survival rather than increased proliferation. The prevalence of survival over proliferation was confirmed by Bcl-2 or Bcl-X L increase in cancer versus mucosa, and by decreased PPAR α . “In vitro” PPAR γ and PPAR α were evaluated in human tumor and normal cell lines, treated with natural or synthetic ligands. PPAR γ was involved in inhibiting cell proliferation with a decrease in c-Myc protein, whereas PPAR α was involved in inducing apoptosis with modulation of Bcl-2 and Bad proteins. This involvement was confirmed using specific antagonists of two PPARs. Moreover, the results obtained on treating cell lines with PPAR ligands confirm observations in colon cancer: there is an inverse correlation between PPAR α and Bcl-2 and between PPAR γ and c-Myc.
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