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

Q2 Biochemistry, Genetics and Molecular Biology Small GTPases Pub Date : 2023-12-01 DOI:10.1080/21541248.2023.2202612
Rosemary Poku, Felix Amissah, Jamie K Alan
{"title":"PI3K Functions Downstream of Cdc42 to Drive Cancer phenotypes in a Melanoma Cell Line.","authors":"Rosemary Poku,&nbsp;Felix Amissah,&nbsp;Jamie K Alan","doi":"10.1080/21541248.2023.2202612","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":22139,"journal":{"name":"Small GTPases","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150613/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small GTPases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/21541248.2023.2202612","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

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.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
PI3K在Cdc42下游发挥作用,驱动黑色素瘤细胞系的癌症表型。
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,包括细胞粘附和运动。最近,在黑色素瘤患者样本中发现了Rho家族GTPase Cdc42的激活突变。此前,我们的工作已经表明PI3K在具有突变活性的Cdc42的下游是重要的。我们目前的研究试图确定PI3K是否是具有BRAF突变的黑色素瘤细胞系中Cdc42的关键下游伴侣,BRAF突变是皮肤黑色素瘤中最常见的突变。在这项工作中,我们能够证明Cdc42有助于增殖、锚定非依赖性生长、细胞运动和侵袭。用pan-PI3K抑制剂治疗能够有效地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下游的一个重要靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Small GTPases
Small GTPases Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
6.10
自引率
0.00%
发文量
6
期刊最新文献
PI3K Functions Downstream of Cdc42 to Drive Cancer phenotypes in a Melanoma Cell Line. ACKnowledging the role of the Activated-Cdc42 associated kinase (ACK) in regulating protein stability in cancer. Serine phosphorylation of the RhoGEF Trio stabilizes endothelial cell-cell junctions. Rab6-mediated retrograde trafficking from the Golgi: the trouble with tubules. To stay in shape and keep moving: MLL emerges as a new transcriptional regulator of Rho GTPases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1