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The dietary charred meat carcinogen 2-Amino-1-Methyl-6-Phenylimidazo[4,5-b]Pyridine acts as both a tumor initiator and promoter in the rat ventral prostate

Johns Hopkins University, Baltimore, Maryland, United States
Cancer Research (Impact Factor: 9.28). 02/2007; 67(3):1378-84. DOI: 10.1158/0008-5472.CAN-06-1336
Source: PubMed

ABSTRACT Exposure of Fisher344 rats to 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP), a heterocyclic amine in cooked meat, causes cancer in the rat ventral prostate, while sparing the dorsolateral and anterior lobes. Uncovering the molecular mechanisms of the lobe specificity of PhIP-induced rat prostate cancer may provide clues to the pathogenesis of human prostate cancer, which is also lobe selective. We examined the prostate and other organs for mutation frequencies using transgenic Fisher344 rats (Big Blue rats) after PhIP treatment. After PhIP treatment for as early as 4 weeks, the colon, spleen, seminal vesicles, and all lobes of the prostate had significantly elevated mutation frequencies compared with the saline-treated control group, and the differences became even greater after 8 weeks. G:C --> T:A transversions were the predominant type of mutation. After 8 weeks of treatment with PhIP, the Ki-67 index was increased (P < 0.001) in the ventral prostate, but not in the dorsolateral or anterior prostate. An increase in the number of stromal mast cells and macrophages was seen in the ventral prostate, but not in the other prostatic lobes. The apoptotic index also increased in the ventral lobe only. The increased proliferation and cell death in response to PhIP indicates that in addition to PhIP acting as an "initiator" of cancer, PhIP is also acting like an organ- and lobe-specific tumor "promoter." The prostate lobe-specific infiltration of mast cells and macrophages in response to PhIP suggests a potential new mechanism by which this dietary compound can increase cancer risk-by prompting inflammation.

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    • "Infiltration of mast cells is the sign of initiation of inflammation. Recent experiments indicate that mast cell infiltration can enhance carcinogenesis [64]–[68] and they have also long been known to drive angiogenesis and tumour growth [67]. In this study, it was observed that there is marked infiltration of mast cells in the sub-mucosal layer in DMH-treated group while there is no mast cells infiltration in control group. "
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