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首页> 外文期刊>Cell death & disease. >Blocking the autocrine regulatory loop of Gankyrin/STAT3/CCL24/CCR3 impairs the progression and pazopanib resistance of clear cell renal cell carcinoma
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Blocking the autocrine regulatory loop of Gankyrin/STAT3/CCL24/CCR3 impairs the progression and pazopanib resistance of clear cell renal cell carcinoma

机译:阻断甘霉/ stat3 / ccl24 / ccr3的自分泌调节回路损害透明细胞肾细胞癌的进展和发挥性抗性

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The poor prognosis of clear-cell renal cell carcinoma (ccRCC) patients is due to progression and targeted drug resistance, but the underlying molecular mechanisms need further elucidation. This study examined the biological function and related mechanisms of gankyrin in ccRCC based on the results of our previous study. To this end, in vitro functional experiments; in vivo models of subcutaneous tumor formation, lung metastasis, and orthotopic ccRCC; and antibody chip detection, co-IP, ChIP assays were performed to examine the biological role and molecular mechanisms of gankyrin in ccRCC. Two hundred fifty-six ccRCC patients were randomly divided into training and validation cohorts to examine the prognostic value of gankyrin and other markers through IHC and statistical analyses. We observed that the gankyrin-overexpressing ccRCC cell lines 786-O and 769-P exhibited increased proliferation, invasion, migration, tumorigenicity, and pazopanib resistance and decreased apoptosis, while gankyrin knockdown achieved the opposite results. Mechanistically, gankyrin recruited STAT3 via direct binding, and STAT3 binding to the CCL24 promoter promoted its expression. Reciprocally, an increase in autocrine CCL24 enhanced the expression of gankyrin and STAT3 activation via CCR3 in ccRCC, forming a positive autocrine-regulatory loop. Furthermore, in vivo experimental results revealed that blocking the positive loop through gankyrin knockdown or treatment with the CCR3 inhibitor SB328437 reversed the resistance to pazopanib and inhibited lung metastasis in ccRCC. Moreover, a positive correlation between gankyrin and STAT3 or CCL24 expression in ccRCC specimens was observed, and improved accuracy for ccRCC patient prognosis was achieved by combining gankyrin and STAT3 or CCL24 expression with existing clinical prognostic indicators, including the TNM stage and SSIGN score. In summary, targeting the gankyrin/STAT3/CCL24/CCR3 autocrine-regulatory loop may serve as a remedy for patients with advanced ccRCC, and combining gankyrin and STAT3 or CCL24 expression with the current clinical indicators better predicts ccRCC patient prognosis.
机译:透明细胞肾细胞癌(CCRCC)患者的预后差是由于进展和靶向耐药性,但潜在的分子机制需要进一步阐明。本研究根据我们以前研究的结果检测了CCRCC中甘霉的生物学功能和相关机制。为此,体外功能实验;在皮下肿瘤形成,肺转移和原位CCRCC的体内模型中;和抗体芯片检测,CO-IP,芯片测定进行,以检测甘库中甘氨酸的生物学作用和分子机制。将两百五十六名CCRCC患者随机分为培训和验证队列,以通过IHC和统计分析检查甘霉和其他标志物的预后价值。我们观察到甘氨酸过度表达的CCRCC细胞系786-O和769-P表现出增加的增殖,侵袭,迁移,致致致致血管抗性和凋亡性降低,而甘氨酸敲低位达到相反的结果。机械地,甘霉素通过直接结合募集STAT3,并且STAT3与CCL24启动子的结合促进其表达。相互作用,自分泌CCL24的增加通过CCR3在CCRCC中增强了甘氨酸和STAT3活化的表达,形成了阳性自分泌调节循环。此外,在体内实验结果表明,通过Gankyrin敲击或用CCR3抑制剂SB328437阻断阳性环,逆转对Pazopanib的抗性并抑制CCRCC中的肺转移。此外,观察到甘霉和STAT3或CCL24表达的阳性相关性,通过将甘霉和STAT3或CCL24表达与现有的临床预后指标组合,包括TNM阶段和SSign评分,提高了CCRCC患者预后的精度。总之,靶向甘氨酸/ stat3 / ccl24 / ccr3自分泌调节回路可以用作高级CCRCC患者的补救措施,并将甘氨酸和STAT3或CCL24表达与当前的临床指标相结合更好地预测CCRCC患者预后。

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