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环状RNA circKDM4B调控肝癌细胞增殖及侵袭迁移的实验研究

Experimental study of circKDM4B on the proliferation,migration and invasion of hepatocellular carcinoma cells
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摘要 目的探索环状RNA circKDM4B对肝癌细胞增殖、凋亡和侵袭迁移的影响,明确其在肝癌进展中所发挥的调控作用。方法采用核糖核酸酶R(RNase R)消化实验和荧光原位杂交实验(FISH)验证circKDM4B的环状结构稳定性及其在细胞中的定位;利用小干扰RNA(siRNA)敲减肝癌细胞circKDM4B的表达,并通过qRT-PCR实验验证敲减效率;采用细胞计数方法(CCK-8)实验、EdU增殖实验检测circKDM4B对肝癌细胞增殖的影响,流式细胞技术检测其对肝癌细胞凋亡的影响;同时应用划痕实验、Transwell实验检测circKDM4B对肝癌细胞迁移侵袭能力的影响。结果相较于线性KDM4B mRNA,circKDM4B对RNase R耐受性更加稳定,FISH结果显示circKDM4B主要定位于肝癌细胞质中;在转染了circKDM4B siRNA后,circKDM4B在肝癌细胞表达下调,而亲本基因KDM4B不受影响。CCK-8和EdU增殖实验结果显示,敲减circKDM4B可抑制肝癌细胞的增殖;流式细胞实验显示敲减circKDM4B可明显促进肝癌细胞凋亡;划痕实验和Transwell实验表明敲减circKDM4B后肝癌细胞的侵袭和迁移能力明显减弱。结论circKDM4B稳定表达于肝癌细胞质中,并具有促进肝癌细胞增殖、侵袭迁移、抑制肝癌细胞凋亡的能力,这提示circKDM4B有望成为新的肝癌治疗靶点。 Objective To clarify the role of circKDM4B on the proliferation,apoptosis,invasion and migration of hepatocellular carcinoma(HCC)cells. Methods In vitro stability of circKDM4B was examined by RNase R treatment,and its location in cells was determined by fluorescence in situ technique(FISH). The expression of circKDM4B was silenced by small interfering RNA(siRNA)in SNU387 and Huh7 cells,respectively,then verified by q RT-PCR. After that,CCK-8 assay,EdU assay,wound healing assay,transwell assays and flow cytometry were used to detect the effects of circKDM4B silencing on HCC cell proliferation,apoptosis,invasion and migration. Results circKDM4B was stable in vitro and not affected by RNase R. FISH showed that circKDM4B was mainly located in cytoplasm.After transfection with si-circKDM4B,the expression levels of circKDM4B were down-regulated. CCK-8,EdU assay and flow cytometry showed that knock-down of circKDM4B significantly inhibited the proliferation ability of HCC cells,and promoted the apoptosis of HCC cells. While wound healing and transwell assay confirmed that knock-down of circKDM4B inhibited the migration and invasion ability of HCC cells. Conclusion circKDM4B is stably located in the cytoplasm of HCC cells,and promotes the proliferation,migration and invasion while inhibits apoptosis of HCC cells,which suggests its potential role as a novel therapy target for HCC.
作者 马晓武 谭文亮 杨磊 谢智钦 王庆斌 陈亚进 商昌珍 MA Xiao-wu;TAN Wen-liang;YANG Lei;XIE Zhi-qin;WANG Qing-bin;CHEN Ya-jin;SHANG Chang-zhen(Department of Hepatobiliary Surgery,Sun Yat-sen Memorial Hospital,Sun Yat-sen University,Guangzhou 510120,China)
出处 《岭南现代临床外科》 2021年第6期614-619,624,共7页 Lingnan Modern Clinics in Surgery
基金 国家自然科学基金(81972263 82072714 82103221) 中国博士后科学基金(2020M683094)。
关键词 肝细胞癌 环状RNA 增殖 凋亡 迁移 hepatocellular carcinoma circKDM4B proliferation apoptosis migration
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  • 1Llovet JM, Burroughs A, Bruix J. Hepatocellular carcinoma.Lancet 2003; 362: 1907-1917 [PMID: 14667750 DOI: 10.1016/S0140-6736(03)14964-1]. 被引量:1
  • 2El-Serag HB. Hepatocellular carcinoma. N Engl J Med 2011; 365:1118-1127 [PMID: 21992124 DOI: 10.1056/NEJMra1001683]. 被引量:1
  • 3Llovet JM, Bruix J. Molecular targeted therapies in hepatocellularcarcinoma. Hepatology 2008; 48: 1312-1327 [PMID: 18821591DOI: 10.1002/hep.22506]. 被引量:1
  • 4Llovet JM, Ricci S, Mazzaferro V, Hilgard P, Gane E, Blanc JF,de Oliveira AC, Santoro A, Raoul JL, Forner A, Schwartz M, PortaC, Zeuzem S, Bolondi L, Greten TF, Galle PR, Seitz JF, BorbathI, Haussinger D, Giannaris T, Shan M, Moscovici M, Voliotis D,Bruix J. Sorafenib in advanced hepatocellular carcinoma. N EnglJ Med 2008; 359: 378-390 [PMID: 18650514 DOI: 10.1056/NEJMoa0708857]. 被引量:1
  • 5Kudo M. Current status of molecularly targeted therapy forhepatocellular carcinoma: clinical practice. Int J Clin Oncol 2010;15: 242-255 [PMID: 20509038 DOI: 10.1007/s10147-010-0089-y]. 被引量:1
  • 6Laurent-Puig P, Zucman-Rossi J. Genetics of hepatocellulartumors. Oncogene 2006; 25: 3778-3786 [PMID: 16799619 DOI:10.1038/sj.onc.1209547]. 被引量:1
  • 7Nejak-Bowen KN, Monga SP. Beta-catenin signaling, liverregeneration and hepatocellular cancer: sorting the good from thebad. Semin Cancer Biol 2011; 21: 44-58 [PMID: 21182948 DOI:10.1016/j.semcancer.2010.12.010]. 被引量:1
  • 8Clevers H, Nusse R. Wnt/兝-catenin signaling and disease. Cell 2012;149: 1192-1205 [PMID: 22682243 DOI: 10.1016/j.cell.2012.05.012]. 被引量:1
  • 9Lee HC, Kim M, Wands JR. Wnt/Frizzled signaling inhepatocellular carcinoma. Front Biosci 2006; 11: 1901-1915[PMID: 16368566]. 被引量:1
  • 10Giles RH, van Es JH, Clevers H. Caught up in a Wnt storm: Wntsignaling in cancer. Biochim Biophys Acta 2003; 1653: 1-24 [PMID:12781368]. 被引量:1

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