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作 者:郭大伟[1] 侯学忠[2] 张宏彬[1] 孙文郁[1] 朱磊[1] 姜晓峰[1] 梁健[1]
机构地区:[1]中国医科大学附属第四医院普外科,辽宁沈阳110032 [2]中国人民解放军463医院普外科,辽宁沈阳110042
出 处:《中国现代医学杂志》2013年第27期54-57,共4页China Journal of Modern Medicine
基 金:2011年辽宁省教育厅科学研究一般项目(No:L2011136)
摘 要:目的研究阻断BDNF及其受体TrkB对人肝癌(HCC)细胞增殖能力的影响,并探讨二者在HCC发生过程中的作用。方法在人HCC细胞系HepG2和97-H中,采用ELISA方法检测BDNF在培养上清中的分泌水平,采用MTT方法测定BDNF中和抗体、干扰BDNF表达或受体酪氨酸激酶(trk)活性抑制剂K252a对细胞增殖的影响。结果 BDNF在HepG2和97-H细胞培养上清中的浓度分别为(88.56±7.45)pg/mL和(119.08±6.21)pg/mL。特异性siRNA转染细胞后,BDNF在HepG2和97-H细胞培养上清中的浓度分别为(73.29±3.63)pg/mL和(102.40±4.01)pg/mL。BDNF中和抗体、干扰BDNF表达或K252a都能有效抑制HepG2和97-H细胞增殖。结论 BDNF/TrkB可能在促进HCC细胞生长方面具有重要作用,有助于HCC的发生发展。[ Objectives ] To investigate the effects of blocking BDNF and its receptor TrkB on the proliferation of human hepatocellular carcinoma (HCC) cells, and explore the relationship between carcinogenesis and their roles in liver. [ Methods ] ELISA was performed to detect the BDNF secretory levels in supematant of HCC cells HepG2 and 97-H. MTT was used to evaluate the effects of BDNF neutralizing anti-body, interfering with BDNF expression, or tyrosine kinase (trk) inhibitor K252a on cell proliferation. [Results ] BDNF content in supernatant of HepG2 and 97-H cells was (88.56±7.45)pg/mL and (119.08±6.21)pg/mL, respectively. BDNF content in supernatant of HepG2 and 97-H cells transfected with specific BDNF-siRNA was (73.29±3.63)pg/mL and (102.40±4.01)pg/mL, respec- tively. When treated with BDNF neutralizing anti-body, BDNF-siRNA or trk inhibitor K252a, cell proliferation was inhibited significantly. [ Conclusions] BDNFFFrkB may play important roles in supporting cell growth and promoting HCC progression.
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