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CHC 通过调控 HIF-1α 和 VEGF 信号通路促进肿瘤生长和血管生成。

CHC promotes tumor growth and angiogenesis through regulation of HIF-1α and VEGF signaling.

机构信息

Institute of Cellular and Organismic Biology, Academia Sinica, Taipei 115, Taiwan.

出版信息

Cancer Lett. 2013 Apr 30;331(1):58-67. doi: 10.1016/j.canlet.2012.12.001. Epub 2012 Dec 8.

Abstract

Pancreatic adenocarcinoma is an aggressive disease with a high mortality rate. In this study, we have newly generated a monoclonal antibody (mAb), Pa65-2, which specifically binds to pancreatic cancer cells and tumor blood vessels. The target protein of Pa65-2 is identified as human clathrin heavy chain (CHC). In vitro and In vivo study showed that suppression of CHC either by shRNA or by Pa65-2 inhibited tumor growth and angiogenesis. One of the key functions of CHC was to bind with the hypoxia-inducing factor (HIF)-1α protein, increasing the stability of this protein and facilitating its nuclear translocation, thereby regulating the expression of VEGF. Taken together, our findings indicate that CHC plays a role in the processes of tumorigenesis and angiogenesis. Pa65-2 antibody or CHC shRNA can potentially be used for pancreatic cancer therapy.

摘要

胰腺导管腺癌是一种具有高死亡率的侵袭性疾病。在这项研究中,我们新生成了一种单克隆抗体(mAb)Pa65-2,它特异性地与胰腺癌细胞和肿瘤血管结合。Pa65-2 的靶蛋白被鉴定为人笼形蛋白重链(CHC)。体外和体内研究表明,通过 shRNA 或 Pa65-2 抑制 CHC 的表达可抑制肿瘤生长和血管生成。CHC 的一个关键功能是与缺氧诱导因子(HIF)-1α蛋白结合,增加该蛋白的稳定性并促进其核转位,从而调节 VEGF 的表达。总之,我们的研究结果表明 CHC 在肿瘤发生和血管生成过程中发挥作用。Pa65-2 抗体或 CHC shRNA 可能可用于胰腺癌的治疗。

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