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dc.contributor.author Takács, Tamás
dc.contributor.author Kudlik, Gyöngyi
dc.contributor.author Kurilla, Anita
dc.contributor.author Szeder, Bálint
dc.contributor.author Buday, László
dc.contributor.author Vas, V.irág
dc.date.accessioned 2021-09-07T11:22:11Z
dc.date.available 2021-09-07T11:22:11Z
dc.date.issued 2020
dc.identifier 85087695741
dc.identifier.citation journalVolume=39;journalIssueNumber=4;journalTitle=CANCER AND METASTASIS REVIEWS;pagerange=1051-1065;journalAbbreviatedTitle=CANCER METAST REV;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8505
dc.identifier.uri doi:10.1007/s10555-020-09912-8
dc.description.abstract The genetic alterations in cancer cells are tightly linked to signaling pathway dysregulation. Ras is a key molecule that controls several tumorigenesis-related processes, and mutations in RAS genes often lead to unbiased intensification of signaling networks that fuel cancer progression. In this article, we review recent studies that describe mutant Ras-regulated signaling routes and their cross-talk. In addition to the two main Ras-driven signaling pathways, i.e., the RAF/MEK/ERK and PI3K/AKT/mTOR pathways, we have also collected emerging data showing the importance of Ras in other signaling pathways, including the RAC/PAK, RalGDS/Ral, and PKC/PLC signaling pathways. Moreover, microRNA-regulated Ras-associated signaling pathways are also discussed to highlight the importance of Ras regulation in cancer. Finally, emerging data show that the signal alterations in specific cell types, such as cancer stem cells, could promote cancer development. Therefore, we also cover the up-to-date findings related to Ras-regulated signal transduction in cancer stem cells. © 2020, The Author(s).
dc.relation.ispartof urn:issn:0167-7659
dc.title The effects of mutant Ras proteins on the cell signalome
dc.type Journal Article
dc.date.updated 2020-09-24T07:28:06Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 31400188
dc.identifier.wos 000546856300002
dc.contributor.department SE/AOK/I/Biokémiai és Molekuláris Biológiai Intézet
dc.contributor.institution Semmelweis Egyetem


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