Literature DB >> 28847905

PI3K: A Crucial Piece in the RAS Signaling Puzzle.

Agata Adelajda Krygowska1, Esther Castellano1.   

Abstract

RAS proteins are key signaling switches essential for control of proliferation, differentiation, and survival of eukaryotic cells. RAS proteins are mutated in 30% of human cancers. In addition, mutations in upstream or downstream signaling components also contribute to oncogenic activation of the pathway. RAS proteins exert their functions through activation of several signaling pathways and dissecting the contributions of these effectors in normal cells and in cancer is an ongoing challenge. In this review, we summarize our current knowledge about how RAS regulates type I phosphatidylinositol 3-kinase (PI3K), one of the main RAS effectors. RAS signaling through PI3K is necessary for normal lymphatic vasculature development and for RAS-induced transformation in vitro and in vivo, especially in lung cancer, where it is essential for tumor initiation and necessary for tumor maintenance.
Copyright © 2018 Cold Spring Harbor Laboratory Press; all rights reserved.

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Year:  2018        PMID: 28847905      PMCID: PMC5983164          DOI: 10.1101/cshperspect.a031450

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Med        ISSN: 2157-1422            Impact factor:   6.915


  201 in total

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Review 5.  Anoikis molecular pathways and its role in cancer progression.

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Review 6.  The Ras-ERK and PI3K-mTOR pathways: cross-talk and compensation.

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Review 7.  RAS oncogenes: weaving a tumorigenic web.

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  13 in total

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Review 7.  The effects of mutant Ras proteins on the cell signalome.

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