Zhao Mei, Liu Feng, Wang Jiong-Yi, Zhang Wen-Ying, Gao Feng-Hou, Jiang Bin
Department of Oncology, the Third People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 201900, China.
Zhonghua Yi Xue Za Zhi. 2011 Feb 15;91(6):375-81.
To investigate the relationship between janus kinase2/signal transducer and activator of transcription 3 (JAK2/STAT3) signaling pathway and angiogenesis in non-small cell lung cancer (NSCLC) and explore the effects on the mRNA expression of vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) by blocking JAK2/STAT3 signaling pathway.
Immunohistochemistry was used to determine the expression of P-JAK2, P-STAT3 and microvessel density (MVD) in 68 NSCLC tissues and 27 normal lung tissues. And the relationship with their clinical pathological features was analyzed. Human lung cancer A549 cells were treated with different concentrations of AG490. Cell proliferation was measured by MTT assay. Western blot was performed to detect the activation of JAK2/STAT3 signaling pathway. The mRNA expressions of VEGF and bFGF were determined by RT-PCR (reverse transcription-polymerase chain reaction). A549 cells were transfected with STAT3 siRNA. And the protein of STAT3, Phos-STAT3 (P-STAT3) and mRNA levels of VEGF and bFGF were detected.
The activation of JAK2/STAT3 signaling pathway was closely related to MVD in NSCLC. AG490 and STAT3 siRNA could block the JAK2/STAT3 signaling pathway and down-regulated the mRNA expressions of VEGF and bFGF in lung cancer cells.
JAK2/STAT3 signaling pathway plays an important role in the angiogenesis of NSCLC. Blocking this pathway may inhibit the expression of angiogenic cytokines. JAK2/STAT3 signaling pathway may be a critical therapeutic target for the treatment of angiogenesis in NSCLC.
探讨非小细胞肺癌(NSCLC)中janus激酶2/信号转导及转录激活因子3(JAK2/STAT3)信号通路与血管生成的关系,并探究阻断JAK2/STAT3信号通路对血管内皮生长因子(VEGF)和碱性成纤维细胞生长因子(bFGF)mRNA表达的影响。
采用免疫组织化学法检测68例NSCLC组织和27例正常肺组织中P-JAK2、P-STAT3的表达及微血管密度(MVD),并分析其与临床病理特征的关系。用不同浓度的AG490处理人肺癌A549细胞,采用MTT法检测细胞增殖,Western blot法检测JAK2/STAT3信号通路的激活情况,逆转录-聚合酶链反应(RT-PCR)法检测VEGF和bFGF的mRNA表达。将STAT3 siRNA转染A549细胞,检测STAT3、磷酸化STAT3(P-STAT3)蛋白及VEGF和bFGF的mRNA水平。
NSCLC中JAK2/STAT3信号通路的激活与MVD密切相关。AG490和STAT3 siRNA可阻断JAK2/STAT3信号通路,下调肺癌细胞中VEGF和bFGF的mRNA表达。
JAK2/STAT3信号通路在NSCLC血管生成中起重要作用。阻断该通路可能抑制血管生成相关细胞因子的表达。JAK2/STAT3信号通路可能是NSCLC血管生成治疗的关键靶点。