TITLE

Possible role of REG lα protein in ulcerative colitis and colitic cancer

AUTHOR(S)
Sekikawa, A.; Fukui, H.; Fujii, S.; Nanakin, A.; Kanda, N.; Uenoyoma, Y.; Sawabu, T.; Hisatsune, H.; Kusaka, T.; Ueno, S.; Nakase, H.; Seno, H.; Fujimori, T.; Chiba, T.
PUB. DATE
October 2005
SOURCE
Gut;Oct2005, Vol. 54 Issue 10, p1437
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Background and aims: Although regenerating gene (REG) lα protein may be involved in the inflammation and carcinogenesis in the gastrointestinal tract, its pathophysiological role in ulcerative colitis (UC) and the resulting colitic cancer remains unclear. We investigated expression of the REG lα gene and its protein in UC and colitic cancer tissues. We examined whether cytokines are responsible for REG lα gene expression and whether REG lot protein has a trophic and/or an antiapoptotic effect on colon cancer cells. Methods: Expression of REG In mRNA and its gene product in UC tissues was analysed by real time reverse transcription-polymerase chain reaction and immunohistochemistry, respectively. The effects of cytokines on REG lα promoter activity were examined in LoVo cells by luciferase reporter assay. The effects of REG lot protein on growth and H2O2 induced apoptosis were examined in LoVo cells by MU and TUNEL assays, respectively. Results: REG lα protein was strongly expressed in inflamed epithelium and in dysplasias and cancerous lesions in UC tissues. The level of REG lα mRNA expression in UC tissues correlated significantly with severity of inflammation and disease duration. REG let promoter activity was enhanced by stimulation with interferon γ or interleukin 6. REG lα protein promoted cell growth and conferred resistance to H2O2 induced apoptosis in LoVo cells. REG lα protein promoted Akt phosphorylation and enhanced Bcl-xL and Bcl-2 expression in LoVo cells. Conclusions: The REG lαgene is inducible by cytokines and its gene product may function as a mitogenic and/or an antiapoptotic factor in the UC-colitic cancer sequence.
ACCESSION #
18457691

 

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