Yu Muming, Lu Bin, Liu Yancun, Me Ying, Wang Lijun, Li Hui
Emergency Department, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, P.R. China.
Mol Med Rep. 2017 Mar;15(3):1103-1108. doi: 10.3892/mmr.2017.6136. Epub 2017 Jan 23.
Tumor cells resistant to anoikis are considered to be candidates for metastasis. In the present study, the role of Tim‑3 in anoikis and its influence on the invasion of clear cell renal cell carcinoma (ccRCC) was investigated. Here, polyhydroxylethylmethacrylate (poly‑HEMA) was applied to two ccRCC cell lines, 786‑O and Caki‑2, to induce detachment from the extracellular matrix (ECM). Tim‑3 mRNA and protein expression levels were assayed by reverse transcription-quantitative polymerase chain reaction (RT‑qPCR) and western blot, respectively. Anoikis was measured by Ho33342/PI double staining, acridine orange staining, and further determined using the CytoSelect™ 24‑well Anoikis Assay kit. Apoptosis was measured using flow cytometry, E‑cadherin and N‑cadherin protein expression were determined using western blotting and a Chemicon cell invasion assay kit was used to quantify the invasive capacity of 786‑O and Caki‑2 cells. It was demonstrated that detachment from the ECM decreases transcription and the protein expression level of Tim‑3 in 786‑O and Caki‑2 cells compared with control cells. Interference with Tim‑3 expression using small interfering RNA exacerbated anoikis in 786‑O and Caki‑2 cells induced by poly‑HEMA treatment. E‑cadherin upregulation, N‑cadherin downregulation, and ECM detachment‑induced reduction in invasion ability were all exacerbated by knockdown of Tim‑3. In conclusion, interference with Tim‑3 expression may attenuate the invasion of renal cell carcinoma by aggravating anoikis, indicating Tim‑3 as a potential therapeutic target for treating ccRCC.
对失巢凋亡具有抗性的肿瘤细胞被认为是转移的候选细胞。在本研究中,研究了Tim-3在失巢凋亡中的作用及其对透明细胞肾细胞癌(ccRCC)侵袭的影响。在此,将聚甲基丙烯酸羟乙酯(poly-HEMA)应用于两种ccRCC细胞系786-O和Caki-2,以诱导其与细胞外基质(ECM)脱离。分别通过逆转录定量聚合酶链反应(RT-qPCR)和蛋白质印迹法检测Tim-3 mRNA和蛋白质表达水平。通过Ho33342/PI双重染色、吖啶橙染色检测失巢凋亡,并使用CytoSelect™ 24孔失巢凋亡检测试剂盒进一步测定。使用流式细胞术检测细胞凋亡,使用蛋白质印迹法测定E-钙黏蛋白和N-钙黏蛋白的蛋白质表达,并使用Chemicon细胞侵袭检测试剂盒定量786-O和Caki-2细胞的侵袭能力。结果表明,与对照细胞相比,与ECM脱离会降低786-O和Caki-2细胞中Tim-3的转录和蛋白质表达水平。使用小干扰RNA干扰Tim-3表达会加剧poly-HEMA处理诱导的786-O和Caki-2细胞的失巢凋亡。Tim-3基因敲低会加剧E-钙黏蛋白上调、N-钙黏蛋白下调以及ECM脱离诱导的侵袭能力降低。总之,干扰Tim-3表达可能通过加重失巢凋亡来减弱肾细胞癌的侵袭,表明Tim-3是治疗ccRCC的潜在治疗靶点。