Visfatin Promotes Renal Cell Carcinoma Progression: Evidence from Clinical Samples and Cell Line Models.

IF 1.9 Q3 ONCOLOGY
Journal of Kidney Cancer and VHL Pub Date : 2025-09-26 eCollection Date: 2025-01-01 DOI:10.15586/jkc.v12i3.427
Eiji Kashiwagi, Miho Ushijima, Shohei Ueda, Yoshihiro Sugita, Yui Mizushima, Takuo Matsukawa, Rieko Kimuro, Kazumasa Jojima, Katsuyoshi Higashijima, Yujiro Nagata, Akinori Minato, Ikko Tomisaki, Masatoshi Eto
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Abstract

The kidney is enveloped by perirenal fat, which secretes various hormones and cytokines, known as adipokines. Adipokines have been demonstrated to influence the development and progression of tumors, including renal cell carcinoma (RCC). Visfatin, an adipokine secreted by the adipose tissue, has been implicated in RCC, but its precise role remains unclear. In this study, we investigated the expression of visfatin in perirenal fat from patients with RCC and its correlation with the RCC malignant phenotype, and we examined the role of visfatin in RCC cell lines in vitro. This study included adipose tissue samples from 57 Japanese patients with clear cell RCC who underwent partial or radical nephrectomy. We examined the mRNA expression level of visfatin using real-time PCR. In vitro MTT assay and western blot were performed using human RCC cell lines. The mRNA expression of visfatin in peri-tumor versus peri-normal fat was higher in Fuhrman grade ≥2 cases compared with Fuhrman grade 1 cases. Furthermore, the addition of visfatin to RCC cell lines promoted cell proliferation, which was accompanied by increased protein expression of HIF1α, p-Akt, and p-ERK. Conversely, the addition of FK866, a visfatin inhibitor, suppressed cell proliferation and reduced these proteins. Our findings suggest that visfatin from peri-tumor adipose tissue influences the malignancy of RCC and plays a role in promoting the growth of RCC. This indicates a potential mechanism by which adipose tissue contributes to the progression of RCC, providing a possible target for therapeutic intervention.

Visfatin促进肾细胞癌进展:来自临床样本和细胞系模型的证据。
肾脏被肾周脂肪包裹,这些脂肪分泌各种激素和细胞因子,即脂肪因子。脂肪因子已被证明影响肿瘤的发生和进展,包括肾细胞癌(RCC)。Visfatin是一种由脂肪组织分泌的脂肪因子,与RCC有关,但其确切作用尚不清楚。在本研究中,我们研究了visfatin在RCC患者肾周脂肪中的表达及其与RCC恶性表型的相关性,并在体外研究了visfatin在RCC细胞系中的作用。本研究包括57名接受部分或根治性肾切除术的日本透明细胞肾细胞癌患者的脂肪组织样本。采用实时荧光定量PCR检测visfatin mRNA表达水平。以人RCC细胞株为实验对象,进行体外MTT和western blot检测。Fuhrman分级≥2的肿瘤周围脂肪中visfatin mRNA表达高于Fuhrman分级为1的肿瘤周围脂肪。此外,在RCC细胞系中添加visfatin可促进细胞增殖,并伴有HIF1α、p-Akt和p-ERK蛋白表达的增加。相反,加入FK866,一种visfatin抑制剂,抑制细胞增殖并减少这些蛋白。我们的研究结果表明,来自肿瘤周围脂肪组织的visfatin影响RCC的恶性程度,并在促进RCC生长中发挥作用。这表明脂肪组织促进RCC进展的潜在机制,为治疗干预提供了可能的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
6.20%
发文量
22
审稿时长
4 weeks
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