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Activation of corticotropin-releasing factor receptor 2 inhibits the growth of human small cell lung carcinoma cells.

机译:促肾上腺皮质激素释放因子受体2的激活抑制人小细胞肺癌细胞的生长。

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摘要

Previously, we found the activation of corticotropin-releasing factor receptor 2 (CRFR2) could inhibit tumor growth via an anti-angiogenic pathway, implying CRFR2 may be a tumor therapeutic target. Here, CRFR2 expression in human neuroendocrine small cell lung carcinoma (SCLC) tissues and cell lines NCI-H446 and NCI-H1688 were detected. Meanwhile, UCNs could directly inhibit the proliferation and promote the apoptosis of SCLC cells via CRFR2. It was also shown that the activation of CRFR2 could inhibit p38 and Akt phosphorylation to suppress the secretion of VEGF in SCLC cells. These observations implied CRFR2 might be a therapeutic target in human SCLC.
机译:以前,我们发现促肾上腺皮质激素释放因子受体2(CRFR2)的激活可以通过抗血管生成途径抑制肿瘤的生长,这暗示CRFR2可能是肿瘤的治疗靶标。在这里,检测到CRFR2在人神经内分泌小细胞肺癌(SCLC)组织和细胞系NCI-H446和NCI-H1688中的表达。同时,UCNs可以通过CRFR2直接抑制SCLC细胞的增殖并促进其凋亡。还显示CRFR2的激活可以抑制p38和Akt磷酸化,从而抑制SCLC细胞中VEGF的分泌。这些观察结果暗示CRFR2可能是人SCLC中的治疗靶标。

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