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Inhibitory effect of linoleic acid on transformation of IEC6 intestinal cells by in vitro azoxymethane treatment
Author(s) -
Sasaki Takamitsu,
Yoshida Kazuhiro,
Shimura Hideo,
Ichiba Masayosi,
Sasahira Tomonori,
Shimomoto Takasumi,
Denda Ayumi,
Kuniyasu Hiroki
Publication year - 2005
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.21393
Subject(s) - azoxymethane , biology , in vitro , microbiology and biotechnology , carcinogenesis , cell growth , receptor , cell culture , endocrinology , dna synthesis , peroxisome proliferator activated receptor , medicine , cancer research , biochemistry , gene , genetics
Abstract The effect of linoleic acid (LA) on growth and transformation of IEC6 intestinal cells was examined. IEC6 cells expressed mRNAs of 15‐lipooxygenase (LOX15) and peroxisome proliferator–activated receptor (PPAR)γ but not COX‐2. Cell growth was suppressed by LA in a dose‐dependent manner in IEC6 cells. Three‐week treatment with LA provided IEC6 cells a quiescent state. LA‐induced growth inhibition was abrogated by exposure to antisense S‐oligodeoxynucleotides (S‐ODNs) for LOX15 and/or PPARγ. In an in vitro carcinogenesis model, IEC6 cells, which had confirmed CYP2E1 expression and activity, were continuously treated with AOM and/or LA for 40 weeks. DNA injury in AOM‐treated cells was suppressed to the control level by concurrent LA treatment. Colony formation of AOM‐treated cells in soft agar was suppressed by treatment with LA, which was reversed by exposure to antisense S‐ODNs for LOX15 and/or PPARγ. AOM‐treated IEC6 cells formed s.c. tumors in 9 of 12 mice, whereas AOM+LA‐treated cells formed no tumor. IEC6 cells showed no remarkable alteration of protein production by AOM treatment, whereas cells treated with AOM+LA showed decreased epidermal growth factor receptor (EGFR) and phospho‐EGFR and increased BAX. These findings suggest that LA inhibited AOM‐induced transformation of COX‐2‐negative IEC6 cells, which was possibly mediated with PPARγ ligands generated by LOX15 from LA. © 2005 Wiley‐Liss, Inc.