6533b831fe1ef96bd1298b2c

RESEARCH PRODUCT

Effet anti-tumoral de l'acide docosahexaénoïque : implication des microARNs et du TNFalpha

Aurélie Fluckiger

subject

[SDV.MHEP] Life Sciences [q-bio]/Human health and pathologyApoptose[ SDV.BC ] Life Sciences [q-bio]/Cellular BiologyAMPKαApoptosisFoxo3a[SDV.BC]Life Sciences [q-bio]/Cellular BiologyAcide docosahexaénoïqueColorectal cancerCancer colorectalDocosahexaenoic acidMiR-21[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathology[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyAMPKaTNFα[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyRIP1[SDV.BC] Life Sciences [q-bio]/Cellular Biology[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular Biology[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

description

Docosahexaenoic acid (DHA) is an omega-3 polyunsaturated fatty acid with anti-inflammatory and anti-tumoral properties. The anti-tumor effect of DHA in colorectal cancer might be attributed to direct anti-proliferative action on cancer cells and to its ability to reduce inflammatory status involved in tumor growth. Tumor Necrosis Factor-alpha (TNFa) is an inflammatory cytokine with paradoxical effect in cancer biology. According to the cellular context, TNFa activates RIP1 kinase dependent signaling pathway leading to proliferation or cell death. Our aim was to evaluate the role of TNFa in anti-proliferative effect of DHA in colon cancer cells and to precise the molecular mechanisms regulating TNFa expression.DHA treatment increased TNFa expression and secretion by cancer cells. We have shown that neutralization of autocrine TNFa action prevented the pro-apoptotic effect of DHA colon cancer cells and abolished anti-cancer effect in tumor HCT-116 bearing nude mice fed a DHA-enriched diet. Induction of TNFa expression by DHA occured at post-transcriptional level through microRNA miR-21 repression reducing its ability to induce TNFa mRNA degradation. DHA activates AMPKa and RIP1 kinases triggering nuclear translocation of the transcription factor Foxo3a which bound to miR-21 promoter and repressed the microRNA expression. Our works highlight a new molecular mechanism supporting the anti-cancer action of DHA.

https://tel.archives-ouvertes.fr/tel-01418773