首页> 外文期刊>World Journal of Gastroenterology >Trans-10,cis-12, not cis-9,trans-11, conjugated linoleic acid decreases ErbB3 expression in HT-29 human colon cancer cells.
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Trans-10,cis-12, not cis-9,trans-11, conjugated linoleic acid decreases ErbB3 expression in HT-29 human colon cancer cells.

机译:反式10,顺式12,而不是顺式9,反式11,共轭亚油酸降低HT-29人结肠癌细胞中ErbB3的表达。

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AIM: To examine whether trans-10,cis-12 CLA (t10c12) or cis-9,trans-11 CLA (c9t11) inhibits heregulin (HRG)-beta-stimulated cell growth and HRG-beta-ErbB3 signaling in HT-29 cells. METHODS: We cultured HT-29 cells in the absence or presence of the CLA isomers and/or the ErbB3 ligand HRG-beta. MTT assay, ((3)H)thymidine incorporation, Annexin V staining, RT-PCR, Western blotting, immunoprecipitation, and in vitro kinase assay were performed. RESULTS: HRG-beta increased cell growth, but did not prevent t10c12-induced growth inhibition. T10c12 inhibited DNA synthesis and induced apoptosis of HT-29 cells, whereas c9t11 had no effect. T10c12 decreased the levels of ErbB1, ErbB2, and ErbB3 proteins and transcripts in a dose-dependent manner, whereas c9t11 had no effect. Immunoprecipitation/Western blot studies revealed that t10c12 inhibited HRG-beta-stimulated phosphorylation of ErbB3, recruitment of the p85 subunit of phosphoinositide 3-kinase (PI3K) to ErbB3, ErbB3-associated PI3K activities, and phosphorylation of Akt. However, c9t11 had no effect on phospho Akt levels. Neither t10c12 nor c9t11 had any effect on HRG-beta-induced phosphorylation of ERK-1/2. CONCLUSION: These results indicate that the inhibition of HT-29 cell growth by t10c12 may be induced via its modulation of ErbB3 signaling leading to inhibition of Akt activation.
机译:目的:检查trans-10,cis-12 CLA(t10c12)或cis-9,trans-11 CLA(c9t11)抑制HT-29中调蛋白(HRG)-β刺激​​的细胞生长和HRG-β-ErbB3信号传导细胞。方法:我们在不存在或存在CLA异构体和/或ErbB3配体HRG-beta的情况下培养HT-29细胞。进行了MTT测定,((3)H)胸苷掺入,膜联蛋白V染色,RT-PCR,蛋白质印迹,免疫沉淀和体外激酶测定。结果:HRG-β增加了细胞生长,但没有阻止t10c12诱导的生长抑制。 T10c12抑制HT-29细胞的DNA合成并诱导其凋亡,而c9t11没有作用。 T10c12以剂量依赖的方式降低了ErbB1,ErbB2和ErbB3蛋白质和转录本的水平,而c9t11没有作用。免疫沉淀/蛋白质印迹研究表明,t10c12抑制HRG-β刺激的ErbB3磷酸化,磷酸肌醇3-激酶(PI3K)的p85亚基募集至ErbB3,与ErbB3相关的PI3K活性和Akt磷酸化。但是,c9t11对磷酸化Akt水平没有影响。 t10c12和c9t11都不对HRG-β诱导的ERK-1 / 2磷酸化产生任何影响。结论:这些结果表明,t10c12对HT-29细胞生长的抑制作用可能是通过其对ErbB3信号的调节而引起的,从而导致对Akt激活的抑制。

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