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4-羟基壬烯醛和过氧化物酶体增殖物激活受体γ配体影响结肠癌细胞的增殖、分化和凋亡。

4-Hydroxynonenal and PPARgamma ligands affect proliferation, differentiation, and apoptosis in colon cancer cells.

作者信息

Cerbone Angelo, Toaldo Cristina, Laurora Stefano, Briatore Federica, Pizzimenti Stefania, Dianzani Mario U, Ferretti Carlo, Barrera Giuseppina

机构信息

Istituto di Ricerche Biomediche A Maxer RBM s.p.a., Colleretto Giocosa, Turin, Italy.

出版信息

Free Radic Biol Med. 2007 Jun 1;42(11):1661-70. doi: 10.1016/j.freeradbiomed.2007.02.009. Epub 2007 Feb 20.

Abstract

PPARgamma ligands inhibit growth and induce apoptosis of various cancer cells. 4-Hydroxynonenal (HNE), a product of lipid peroxidation, inhibits proliferation and induces differentiation or apoptosis in neoplastic cells. The aim of this work was to investigate the effects of PPARgamma ligands (rosiglitazone and 15-deoxy-prostaglandin J2 (15d-PGJ2)) and HNE, alone or in association, on proliferation, apoptosis, differentiation, and growth-related and apoptosis-related gene expression in colon cancer cells (CaCo-2 cells). PPARgamma ligands inhibited cell proliferation (IC50 was 37.47+/-6.6 microM, for 15d-PGJ2, and 170.34+/-20 microM for rosiglitazone). HNE (1 microM) inhibited cell growth by 70%. Apoptosis was induced by 15d-PGJ2 and HNE and, to a minor extent, rosiglitazone. Differentiation was induced by rosiglitazone and by 15d-PGJ2, but not by HNE. PPARgamma ligands inhibited c-myc expression. HNE induced a transitory increase in c-myc expression and a subsequent down-regulation. HNE induced p21 expression, whereas PPARgamma ligands did not. Expression of the bax gene was increased by HNE and 15d-PGJ2, but not by rosiglitazone. No synergism or antagonism was found between HNE and PPARgamma ligands. Both apoptosis and differentiation induction may be responsible for the inhibition of proliferation by PPARgamma ligands; apoptosis and c-myc and p21 expression seem to be involved in the inhibition of proliferation by HNE.

摘要

过氧化物酶体增殖物激活受体γ(PPARγ)配体可抑制多种癌细胞的生长并诱导其凋亡。4-羟基壬烯醛(HNE)是脂质过氧化的产物,可抑制肿瘤细胞的增殖并诱导其分化或凋亡。本研究旨在探讨PPARγ配体(罗格列酮和15-脱氧前列腺素J2(15d-PGJ2))以及HNE单独或联合使用对结肠癌细胞(CaCo-2细胞)增殖、凋亡、分化以及与生长和凋亡相关基因表达的影响。PPARγ配体可抑制细胞增殖(15d-PGJ2的半数抑制浓度(IC50)为37.47±6.6微摩尔,罗格列酮为170.34±20微摩尔)。HNE(1微摩尔)可使细胞生长抑制70%。15d-PGJ2和HNE可诱导凋亡,罗格列酮在较小程度上也可诱导凋亡。罗格列酮和15d-PGJ2可诱导分化,但HNE不能。PPARγ配体可抑制c-myc的表达。HNE可诱导c-myc表达短暂升高,随后下调。HNE可诱导p21表达,而PPARγ配体则不能。HNE和15d-PGJ2可增加bax基因的表达,但罗格列酮不能。未发现HNE与PPARγ配体之间存在协同或拮抗作用。凋亡和分化诱导可能是PPARγ配体抑制增殖的原因;凋亡以及c-myc和p21表达似乎参与了HNE对增殖的抑制作用。

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