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作 者:郭新[1] 张艳敏[1] 孙亮[1] 周亮[1] 王勇[1] 漆正宇[1] 秦洁[1] 李贤新[1] 陈静[1] 桂耀庭[1] 蔡志明[2]
机构地区:[1]男性生殖和遗传广东省重点实验室北京大学深圳医院,深圳518036 [2]深圳北京大学香港科技大学医学中心
出 处:《临床泌尿外科杂志》2011年第8期589-593,共5页Journal of Clinical Urology
基 金:2010年度市科技研发资金基础研究计划资助项目(编号JC201005260214A);广东省医学科研基金(编号B2009230);深圳市科技计划重点项目(编号201001014);高等学校博士学科点专项科研基金(编号20090001120130);深圳重大疾病临床资料和生物资源标本库;深圳市生物;互联网;新能源产业发展专项资金-公共技术服务平台(编号CXC201005260001A)
摘 要:目的:探讨LIN28在膀胱癌组织和细胞系中表达情况,以及与microRNA初级Let-7g(pri-Let-7g)之间关系,推测其可能临床意义及对肿瘤进展的影响。方法:采用常规RT-PCR、miRNA转录、免疫荧光和免疫组化方法,检测LIN28 mRNA和pri-Let-7g表达,以及LIN28蛋白表达定位。结果:2例膀胱癌细胞系均表达LIN28 mRNA,T24表达较强,免疫荧光显示这两个细胞系均表达LIN28蛋白,阳性部位位于细胞胞质,T24荧光强度强于5637。所选10例膀胱癌和相应癌旁组织均表达LIN28 mRNA,二者并无明显不同,与临床分级也无明确关系。免疫组化显示癌组织LIN28表达阳性并定位于胞质,而癌旁正常组织LIN28表达为阴性。此外,两个细胞系pri-Let-7g表达较强,而癌和癌旁组织的pri-Let-7g表达强度无明显差异,需进一步检测其成熟Let-7g在这些组织中是否存在不同,以明确这些miRNA是否发生生物合成的转录后阻断。结论:明确T24和5637两个膀胱癌细胞系均可作为研究LIN28、Let-7与其相应靶基因关系的体外实验模型。尽管并不确定膀胱癌和癌旁组织LIN28、Let-7g表达强度与临床分级是否相关,但至少明确LIN28/LIN28在膀胱癌中表达,为探讨LIN28和Let-7在泌尿系统来源的其他恶性肿瘤中的作用提供借鉴和实验依据。Objective:To investigate the expression of LIN28 and microRNA primary Let-7g (pri-Let-7g) in bladder cancer and bladder cancer cell lines, as well as to speculate its possible clinical significance and impact on tumor progression. Methods: RT-PCR and miRNA transcription were performed to detect the expression of LIN28 and pri-Let-7g in bladder tissue and bladder cancer cell lines^Immunofluorescence and Immunohistochemistry were used to detect the LIN28 protein location on bladder tissue and Cell lines. Results: LIN28 mRNA was detected in T24 and 5637 cell lines,and its level was higher in T24 than that of 5637. LIN28 protein was located in the cyto- plasm of T24 and 5637. The LIN28 mRNA and pri-Let-7g were expressed in 10 paired tissue samples,and signifi- cant differences were not existed in bladder cancer and adjacent normal tissues, respectively. Moreover, the obvious relationship between the clinical classification and the levels of LIN28 mRNA or pri-Let-7g was not indicated. The mature Let-7g should be detectd in further study to identify whether miRNA Let-7g occurred post-transcriptional block in miRNA biosynthesis. In addition,the pri-Let-7g was also expressed in T24 and 5637 cell lines. The immu- nohistochemistry results were indicated that LIN28 was positive in cancer tissues but was negative in adjacent nor- mal tissues. Conclusions..T24 and 5637 bladder cancer cell lines can be servedd as models to explore the relationship between LIN28 and Let-7 with its associated target genes in vitro. Although this relationship is not evident for the expression level of LIN28 or Let-7g and clinical classification,it is clear that LIN28/LIN28 is expressed in bladder cancer. This study will provide the reference and experimental dates for the other cancer of the urinary system.
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