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首页> 外文期刊>European Journal of Inflammation >Silencing of Yap Gene Inhibits Metastasis in a Severe Combined Immune Deficiency Mice Orthotopic Implantation Gastric Cancer Model:
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Silencing of Yap Gene Inhibits Metastasis in a Severe Combined Immune Deficiency Mice Orthotopic Implantation Gastric Cancer Model:

机译:Yap基因沉默抑制严重联合免疫缺陷小鼠原位植入胃癌模型中的转移:

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YAP signaling has been proved to be involved in cell growth, invasion and metastasis in multiple malignancies. But little has been reported about the effects of YAP transduction on gastric cancer metastases. The present study was aimed to explore the effects of shRNA-mediated targeting of YAP gene on human gastric cancer metastases in severe combined immune deficiency (SCID) mice. Human gastric carcinoma cell line SGC7901 was implanted into the stomach of SCID mice, which were randomly divided into 3 groups (n=10). Via intraperitoneal injection, mice received YAP-shRNA, negative control, or normal saline respectively. The results of TUNEL and FQ-PCR showed an obvious induction of apoptosis in the YAP-shRNA group. Intratumoral vascular density and lymphatic density were suppressed in the YAP-shRNA group. In conclusion, silencing of YAP gene effectively induces the cell apoptosis and inhibits microvascular angiogenesis and lymphagiogenesis of gastric cancer cells in vivo, suggesting that YAP may serve as a promising therapeutic target for treatment of cancer.
机译:YAP信号已被证明参与多种恶性肿瘤的细胞生长,侵袭和转移。但是,关于YAP转导对胃癌转移的影响的报道很少。本研究旨在探讨shRNA介导的YAP基因靶向对严重联合免疫缺陷(SCID)小鼠的人胃癌转移的影响。将人胃癌细胞系SGC7901植入SCID小鼠的胃中,将其随机分为3组(n = 10)。通过腹膜内注射,小鼠分别接受YAP-shRNA,阴性对照或生理盐水。 TUNEL和FQ-PCR的结果显示YAP-shRNA组细胞凋亡明显诱导。 YAP-shRNA组的瘤内血管密度和淋巴密度被抑制。综上所述,YAP基因的沉默有效诱导了胃癌细胞在体内的细胞凋亡,并抑制了微血管血管生成和淋巴管生成,这提示YAP可能成为有希望的治疗癌症的靶标。

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