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SOX7在肾细胞癌中的表达及其对肾癌细胞生物学行为的影响
引用本文:张晓宇,苏建志,任宗涛,刘彬,张爱莉. SOX7在肾细胞癌中的表达及其对肾癌细胞生物学行为的影响[J]. 江苏大学学报(医学版), 2022, 32(2): 124-130,135. DOI: 10.13312/j.issn.1671-7783.y210163
作者姓名:张晓宇  苏建志  任宗涛  刘彬  张爱莉
作者单位:(河北医科大学第四医院泌尿外科,河北 石家庄 050000)
基金项目:河北省卫生厅科技成果推广课题
摘    要:目的:研究Y性别决定基因7(sex determining region Y-box7,SOX7)在肾细胞癌的表达以及对肾癌细胞生物学行为的影响.方法:qRT-PCR和甲基化特异性PCR(MSP)检测SOX7在肾细胞癌组织和肾癌细胞(A498、ACHN、786-O)中的mRNA表达及甲基化状态;免疫组织化学法(immu...

关 键 词:SOX7  肾细胞癌  免疫组化  甲基化状态  功能实验
收稿时间:2021-10-25

Expression of SOX7 in renal cell carcinoma and its effect on the biological behavior of renal cancer cells
ZHANG Xiaoyu,SU Jianzhi,REN Zongtao,LIU Bin,ZHANG Aili. Expression of SOX7 in renal cell carcinoma and its effect on the biological behavior of renal cancer cells[J]. Journal of Jiangsu University Medicine Edition, 2022, 32(2): 124-130,135. DOI: 10.13312/j.issn.1671-7783.y210163
Authors:ZHANG Xiaoyu  SU Jianzhi  REN Zongtao  LIU Bin  ZHANG Aili
Affiliation:(Department of Urology, the Fourth Hospital of Hebei Medical University, Shijiazhuang Hebei 050000, China)
Abstract:Objective: To investigate the expression of sex determining region Y-box 7(SOX7) in renal cell carcinoma and the effect on the biological behavior of renal cancer cells. Methods:  qRT-PCR and methylation specific PCR (MSP) were used to detect the expression and methylation status of SOX7 in renal cell carcinoma tissues and renal cancer cells (A498, ACHN, 786 O); immunohistochemistry (IHC) was used to detect the protein expression of SOX7 in renal cell carcinoma tissues. The SOX7 mRNA expression in renal cancer cells after 5-Aza-dC/TSA intervention was also detected by qRT-PCR. After transfection of SOX7 overexpression plasmid in renal cancer cells ACHN, cell proliferation, migration and invasion were detected by MTS, clone formation, scratch assay and Transwell assay, respectively. Results:  The qRT-PCR and IHC results showed that the expression of SOX7 mRNA and protein in renal cancer tissues was significantly lower than that in paraneoplastic tissues (P<0.01) and correlated with lymph node metastasis and TNM grade (P<0.05). SOX7 mRNA expression in three renal cancer cells (A498, ACHN, 786 O) was significantly lower than that in the control group HK-2 (P<0.01). SOX7 mRNA expression was increased after 5-Aza-dC/TSA treatment in all (P<0.01). MSP results showed that the methylation rate of SOX7 was significantly higher in kidney cancer tissues than that in paraneoplastic tissues (P<0.01) and correlated with TNM stage (P<0.05). Overexpression of SOX7 inhibited the proliferative activity, migration ability and invasive ability of ACHN. Conclusion:  SOX7 is lowly expressed in renal cell carcinoma, hypermethylation of SOX7 may be one of the molecular mechanisms of renal carcinoma histogenesis.
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