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通过凋亡途径拮抗5-HT7受体作为胃癌的一个有前景的靶点

Antagonism of 5-HT7 Receptors as a Promising Target for Gastric Cancer via Apoptotic Pathway.

作者信息

Cinar Irfan, Dincer Busra, Cadirci Elif, Kara Salih, Yildirgan Mehmet Ilhan, Halici Zekai, Palabiyik-Yucelik Saziye Sezin

机构信息

Department of Pharmacology, Faculty of Medicine, Kastamonu University, Kastamonu, Türkiye.

Department of Pharmacology, Faculty of Pharmacy, Ondokuz Mayıs University, Samsun, Türkiye.

出版信息

J Biochem Mol Toxicol. 2025 Jun;39(6):e70326. doi: 10.1002/jbt.70326.

Abstract

Although current treatment strategies have improved clinical outcomes for gastric cancer, they present a challenging prognosis that necessitates novel therapeutic approaches. The 5-HT7 receptor, a member of the serotonin receptor family, plays a significant role in influencing the pathogenesis of various cancer types. This study seeks to investigate the complex interactions among 5-HT7 receptors, gastric cancer, and apoptotic processes. A comprehensive set of experimental techniques was employed, including in vitro staining assays for apoptosis assessment, real-time PCR, and cell proliferation assays. The findings indicate that the 5-HT7 receptor agonist enhances the proliferation of primary gastric tissue cancer cells and KATO-III cells, whereas treatment with the 5-HT7 receptor antagonist significantly inhibits cellular proliferation. Analysis of 5-HT7 receptor mRNA expression in gastric cancer patient populations indicated significantly elevated levels in cancerous tissues when compared to those in healthy tissues. The administration of a 5-HT7 receptor agonist (LP44) resulted in increased cell proliferation in primary gastric cancer cells and KATO-III cell lines, whereas treatment with a 5-HT7 receptor antagonist (SB-269970) significantly inhibited proliferation. Additionally, KATO-III cells treated with the 5-HT7 receptor antagonist demonstrated a marked upregulation of caspase-3, caspase-9, and BAX gene mRNA levels. In contrast, treatment with the 5-HT7 receptor antagonist was associated with a significant reduction in the expression of nuclear factor kappa B and 5-HT7 receptor mRNA levels. Annexin V-FITC/PI and Hoechst 33342 staining demonstrated a pronounced apoptotic effect through antagonism of 5-HT7 receptors compared to other groups. Collectively, the findings of this study suggest that the enhanced expression of 5-HT7 receptors influences gastric cancer formation by regulating the apoptotic axis. This provides a novel perspective for understanding the molecular mechanisms underlying the potential of 5-HT7 receptors as a targeted approach for combating gastric cancer via the apoptotic pathway.

摘要

尽管当前的治疗策略已改善了胃癌的临床结局,但它们仍呈现出具有挑战性的预后,这需要新的治疗方法。5-羟色胺7(5-HT7)受体是血清素受体家族的一员,在影响各种癌症类型的发病机制中起着重要作用。本研究旨在探究5-HT7受体、胃癌和凋亡过程之间的复杂相互作用。采用了一套全面的实验技术,包括用于凋亡评估的体外染色测定、实时聚合酶链反应(PCR)和细胞增殖测定。研究结果表明,5-HT7受体激动剂可增强原发性胃组织癌细胞和KATO-III细胞的增殖,而用5-HT7受体拮抗剂治疗则显著抑制细胞增殖。对胃癌患者群体中5-HT7受体信使核糖核酸(mRNA)表达的分析表明,与健康组织相比,癌组织中的水平显著升高。给予5-HT7受体激动剂(LP44)导致原发性胃癌细胞和KATO-III细胞系中的细胞增殖增加,而用5-HT7受体拮抗剂(SB-269970)治疗则显著抑制增殖。此外,用5-HT7受体拮抗剂处理的KATO-III细胞显示半胱天冬酶-3、半胱天冬酶-9和BAX基因mRNA水平显著上调。相比之下,用5-HT7受体拮抗剂治疗与核因子κB和5-HT7受体mRNA水平的表达显著降低有关。膜联蛋白V-异硫氰酸荧光素/碘化丙啶(Annexin V-FITC/PI)和Hoechst 33342染色显示,与其他组相比,通过拮抗5-HT7受体具有明显的凋亡作用。总体而言,本研究结果表明,5-HT7受体表达增强通过调节凋亡轴影响胃癌形成。这为理解5-HT7受体作为通过凋亡途径对抗胃癌的靶向方法的潜力背后的分子机制提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/120c/12147198/18e4c6346d02/JBT-39-e70326-g008.jpg

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