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首页> 外文期刊>Digestive Diseases and Sciences >Effect of Adiponectin and Ghrelin on Apoptosis of Barrett Adenocarcinoma Cell Line
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Effect of Adiponectin and Ghrelin on Apoptosis of Barrett Adenocarcinoma Cell Line

机译:脂联素和Ghrelin对Barrett腺癌细胞株凋亡的影响

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摘要

Background Obesity is an important risk factor for Barrett adenocarcinoma. However, the role of adiponectin (anti-inflammatory adipokine from adipose tissue) and ghrelin (orexigenic peptide gastric origin) on the progression of Barrett’s carcinogenesis has not been investigated so far. The aim of the present study was: (1) to compare the expression of adiponectin and ghrelin receptors in Barrett’s esophagus and in normal squamous epithelium; (2) to assess the effect of adiponectin and ghrelin on apoptosis in Barrett’s adenocarcinoma cells in vitro; and (3) to investigate the effect of ghrelin on IL-1β and COX-2 expression in OE-19 cells incubated with TNFα. Methods The expression of ghrelin and adiponectin receptors (GHS-R1a, Adipo-R1, Adipo R-2) in biopsies from Barrett’s esophagus and in Barrett’s adenocarcinoma cell line OE-19 was assessed by quantitative RT-PCR (qRT-PCR). The OE-19 cells were also incubated with adiponectin (5–10 μg/ml), and the apoptosis and proliferation were assessed by FACS and MTT assays. Additionally, effects of adiponectin on the mRNA and protein expression of proapoptotic Bax and antiapoptotic Bcl-2 were assessed by RT-PCR and Western blot, respectively. In two different in vitro models of esophagitis the OE-19 cells were incubated with ghrelin alone or in the presence of TNFα or bile acids in the normal or pulse acidified medium, and the expression of IL-1β and COX-2 as markers for inflammation were assessed by FACS and qRT-PCR, respectively. Results Adiponectin caused a significant increase in apoptosis, and this affect was accompanied by increased Bax and decreased Bcl-2 expression. In contrast, ghrelin had no effect on apoptosis of OE-19 cells incubated in neutral or acidified medium with or without addition of deoxycholic acid. At the mRNA level, the expression of adiponectin receptors (Adipo-R1, Adipo-R2) was decreased, and the expression of ghrelin receptor (GHS-R1a) was increased in Barrett’s mucosa. Ghrelin caused a decrease in TNFα-induced COX-2 and IL-1β expression in OE-19 cells. Conclusion Adiponectin and ghrelin have an inhibitory effect on Barrett’s carcinogenesis by two different mechanisms: (1) by an increase in apoptosis by adiponectin, and (2) by anti-inflammatory actions of ghrelin. The decrease in levels of these two peptides in obesity may explain the progression of Barrett’s carcinoma in obese individuals.
机译:背景肥胖是巴雷特腺癌的重要危险因素。然而,迄今为止,尚未研究脂联素(来自脂肪组织的抗炎脂肪因子)和生长素释放肽(胃源性肽)在巴雷特癌变过程中的作用。本研究的目的是:(1)比较脂联素和生长素释放肽受体在巴雷特食管和正常鳞状上皮中的表达; (2)评估脂联素和生长素释放肽对Barrett腺癌细胞体外凋亡的影响; (3)研究ghrelin对与TNFα一起孵育的OE-19细胞中IL-1β和COX-2表达的影响。方法通过定量RT-PCR(qRT-PCR)评估生长素释放肽和脂联素受体(GHS-R1a,Adipo-R1,Adipo R-2)在巴雷特食管和巴雷特腺癌细胞系OE-19中的表达。 OE-19细胞也与脂联素(5-10μg/ ml)一起孵育,并通过FACS和MTT分析评估其凋亡和增殖。另外,分别通过RT-PCR和Western印迹评估脂联素对促凋亡Bax和抗凋亡Bcl-2的mRNA和蛋白表达的影响。在两种不同的食管炎体外模型中,将OE-19细胞单独与生长素释放肽一起孵育,或者在正常或脉冲酸化的培养基中在TNFα或胆汁酸存在下孵育,并将IL-1β和COX-2的表达作为炎症标记物通过FACS和qRT-PCR分别评估。结果脂联素引起细胞凋亡显着增加,这种影响伴随Bax升高和Bcl-2表达降低。相反,生长素释放肽对在添加或不添加脱氧胆酸的中性或酸化培养基中温育的OE-19细胞的凋亡没有影响。在mRNA水平上,巴雷特黏膜中脂联素受体(Adipo-R1,Adipo-R2)的表达降低,而生长素释放肽受体(GHS-R1a)的表达则增加。 Ghrelin导致OE-19细胞中TNFα诱导的COX-2和IL-1β表达降低。结论脂联素和生长激素释放肽通过两种不同的机制抑制Barrett的癌变:(1)脂联素增加细胞凋亡;(2)生长激素释放肽的抗炎作用。肥胖症中这两种肽水平的下降可能解释了肥胖个体中Barrett癌的进展。

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