Zhang Hai-Ping, Zou Jian, Xu Zhuo-Qun, Ruan Jun, Yang Shu-Dong, Yin Ying, Mu Hui-Jun
Department of Derma Science Laboratory, Wuxi No. 2 People's Hospital Affiliated to Nanjing Medical University, Wuxi, Jiangsu 214002, P.R. China.
Department of Clinical Laboratory Science, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, Jiangsu 214023, P.R. China.
Oncol Lett. 2017 Jan;13(1):463-468. doi: 10.3892/ol.2016.5408. Epub 2016 Nov 22.
Although an association between obesity and the occurrence of renal cell carcinoma (RCC) has been identified, the mechanism by which obesity functions to increase this risk of cancer remains unclear. Leptin, visfatin, apelin, resistin and adiponectin are peptide hormones secreted by adipocytes; it is considered that these may affect RCC development by exerting effects on proliferation, cell growth and inflammation. The aim of the present study was to investigate the association between the aforementioned adipokine genes and clear cell RCC (CC-RCC). The GSE6344 dataset was downloaded from the Gene Expression Omnibus database, and the relative expression levels of the adipokine genes were analyzed. To verify the results of the mRNA microarray, 77 paired samples of CC-RCC and corresponding adjacent normal tissue were allocated into two groups. The extraction of total RNA was conducted, and the mRNA expression of adipokine genes was analyzed using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The data from the GSE6344 dataset indicated that the expression of visfatin and apelin was upregulated (P<0.0001 and P<0.01, respectively), and adiponectin was downregulated (P<0.001) in the CC-RCC tissues compared with the adjacent normal tissues. The data from RT-qPCR demonstrated that visfatin and resistin gene expression was increased (P<0.01 and P<0.05, respectively) in the CC-RCC tissues. Furthermore, the mRNA expression level of leptin and adiponectin in the adjacent normal tissue was higher than those in the cancer tissue (P<0.01). The current study verifies that visfatin and adiponectin are associated with an increased risk of CC-RCC, which presents further insights into the molecular mechanisms of CC-RCC tumorigenesis.
尽管肥胖与肾细胞癌(RCC)的发生之间的关联已被确定,但肥胖增加癌症风险的作用机制仍不清楚。瘦素、内脂素、脂联素、抵抗素和脂联素是脂肪细胞分泌的肽类激素;据认为,这些激素可能通过对增殖、细胞生长和炎症产生影响来影响RCC的发展。本研究的目的是调查上述脂肪因子基因与透明细胞RCC(CC-RCC)之间的关联。从基因表达综合数据库下载了GSE6344数据集,并分析了脂肪因子基因的相对表达水平。为了验证mRNA微阵列的结果,将77对CC-RCC和相应的癌旁正常组织样本分为两组。进行总RNA提取,并使用逆转录定量聚合酶链反应(RT-qPCR)分析脂肪因子基因的mRNA表达。来自GSE6344数据集的数据表明,与癌旁正常组织相比,CC-RCC组织中内脂素和脂联素的表达上调(分别为P<0.0001和P<0.01),而脂联素表达下调(P<0.001)。RT-qPCR数据表明,CC-RCC组织中内脂素和抵抗素基因表达增加(分别为P<0.01和P<0.05)。此外,癌旁正常组织中瘦素和脂联素的mRNA表达水平高于癌组织(P<0.01)。当前研究证实内脂素和脂联素与CC-RCC风险增加相关,这为CC-RCC肿瘤发生的分子机制提供了进一步的见解。