Department of Urinary Surgery, Gongli Hospital, Second Military Medical University (Naval Medical University), 219 Miaopu Road, Shanghai, 200135, China.
Department of Urology, the Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, 29 Xinglong Road, Changzhou, Jiangsu, 213000, China.
Cell Death Dis. 2020 Feb 12;11(2):117. doi: 10.1038/s41419-020-2306-6.
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.
透明细胞肾细胞癌(ccRCC)患者的预后较差是由于进展和靶向药物耐药,但潜在的分子机制仍需进一步阐明。本研究基于我们之前的研究结果,探讨了 gankyrin 在 ccRCC 中的生物学功能及相关机制。为此,进行了体外功能实验、皮下肿瘤形成、肺转移和原位 ccRCC 体内模型以及抗体芯片检测、co-IP、ChIP 检测,以研究 gankyrin 在 ccRCC 中的生物学作用和分子机制。随机将 256 例 ccRCC 患者分为训练和验证队列,通过 IHC 和统计分析检测 gankyrin 和其他标志物的预后价值。我们观察到,gankyrin 过表达的 ccRCC 细胞系 786-O 和 769-P 表现出增殖、侵袭、迁移、致瘤性和帕唑帕尼耐药性增加,而凋亡减少,而 gankyrin 敲低则取得了相反的结果。机制上,gankyrin 通过直接结合募集 STAT3,STAT3 结合 CCL24 启动子促进其表达。反过来,自分泌 CCL24 的增加通过 CCR3 增强 ccRCC 中 gankyrin 和 STAT3 激活的表达,形成正的自分泌调节环。此外,体内实验结果表明,通过 gankyrin 敲低或 CCR3 抑制剂 SB328437 阻断正反馈环可逆转帕唑帕尼耐药并抑制 ccRCC 的肺转移。此外,在 ccRCC 标本中观察到 gankyrin 和 STAT3 或 CCL24 表达之间存在正相关,通过将 gankyrin 和 STAT3 或 CCL24 表达与现有的临床预后指标(包括 TNM 分期和 SSIGN 评分)相结合,可提高 ccRCC 患者预后的准确性。综上所述,靶向 gankyrin/STAT3/CCL24/CCR3 自分泌调节环可能成为晚期 ccRCC 患者的治疗方法,将 gankyrin 和 STAT3 或 CCL24 表达与当前临床指标相结合,可更好地预测 ccRCC 患者的预后。