Ran Is a Potential Therapeutic Target for Cancer Cells with Molecular Changes Associated with Activation of the PI3K/Akt/mTORC1 and Ras/MEK/ERK Pathways


Autoria(s): Yuen, Hin-Fung; Chan, Ka Kui; Grills, Claire; Murray, James T.; Platt-Higgins, Angela; Eldin, Osama Sharaf; O'Byrne, Ken; Janne, Pasi; Fennell, Dean A.; Johnston, Patrick G.; Rudland, Philip S.; El-Tanani, Mohamed
Data(s)

15/01/2012

Resumo

Purpose: Cancer cells have been shown to be more susceptible to Ran knockdown than normal cells. We nowinvestigate whether Ran is a potential therapeutic target of cancers with frequently found mutations that lead to higher Ras/MEK/ERK [mitogen-activated protein/extracellular signal-regulated kinase (ERK; MEK)] and phosphoinositide 3-kinase (PI3K)/Akt/mTORC1 activities.

Identificador

http://pure.qub.ac.uk/portal/en/publications/ran-is-a-potential-therapeutic-target-for-cancer-cells-with-molecular-changes-associated-with-activation-of-the-pi3kaktmtorc1-and-rasmekerk-pathways(51edc196-3a53-4266-bdd8-f0dd8302d319).html

http://dx.doi.org/10.1158/1078-0432.CCR-11-2035

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Yuen , H-F , Chan , K K , Grills , C , Murray , J T , Platt-Higgins , A , Eldin , O S , O'Byrne , K , Janne , P , Fennell , D A , Johnston , P G , Rudland , P S & El-Tanani , M 2012 , ' Ran Is a Potential Therapeutic Target for Cancer Cells with Molecular Changes Associated with Activation of the PI3K/Akt/mTORC1 and Ras/MEK/ERK Pathways ' Clinical Cancer Research , vol 18 , no. 2 , pp. 380-391 . DOI: 10.1158/1078-0432.CCR-11-2035

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1300/1306 #Cancer Research #/dk/atira/pure/subjectarea/asjc/2700/2730 #Oncology
Tipo

article