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PI3K 在下游的 Cdc42 驱动黑色素瘤细胞系中的癌症表型。

PI3K Functions Downstream of Cdc42 to Drive Cancer phenotypes in a Melanoma Cell Line.

机构信息

College of Medicine, Central Michigan University, Mt. Pleasant, MI, USA.

Department of Pharmaceutical Science, Ferris State University, Big Rapids, MI, USA.

出版信息

Small GTPases. 2023 Dec;14(1):1-13. doi: 10.1080/21541248.2023.2202612.

Abstract

Rho proteins are part of the Ras superfamily, which function to modulate cytoskeletal dynamics including cell adhesion and motility. Recently, an activating mutation in Cdc42, a Rho family GTPase, was found in a patient sample of melanoma. Previously, our work had shown the PI3K was important downstream of mutationally active Cdc42. Our present study sought to determine whether PI3K was a crucial downstream partner for Cdc42 in a melanoma cells line with a BRAF mutation, which is the most common mutation in cutaneous melanoma. In this work we were able to show that Cdc42 contributes to proliferation, anchorage-independent growth, cell motility and invasion. Treatment with a pan-PI3K inhibitor was able to effectively ameliorate all these cancer phenotypes. These data suggest that PI3K may be an important target downstream of Cdc42 in melanoma.

摘要

Rho 蛋白是 Ras 超家族的一部分,其功能是调节细胞骨架动力学,包括细胞黏附和运动。最近,在黑色素瘤患者样本中发现了 Cdc42(一种 Rho 家族 GTP 酶)的激活突变。此前,我们的工作表明,PI3K 是突变激活的 Cdc42 的下游重要组成部分。本研究旨在确定在具有 BRAF 突变的黑色素瘤细胞系中,PI3K 是否是 Cdc42 的关键下游伙伴,BRAF 突变是皮肤黑色素瘤中最常见的突变。在这项工作中,我们能够表明 Cdc42 促进增殖、非锚定依赖性生长、细胞迁移和侵袭。用 pan-PI3K 抑制剂处理能够有效改善所有这些癌症表型。这些数据表明,PI3K 可能是黑色素瘤中 Cdc42 的下游重要靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fea/10150613/9d0c93dc766d/KSGT_A_2202612_F0001_B.jpg

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