Results 41 to 50 of about 380,814 (333)

κB-Ras Proteins Regulate Both NF-κB-Dependent Inflammation and Ral-Dependent Proliferation

open access: yesCell Reports, 2014
The transformation of cells generally involves multiple genetic lesions that undermine control of both cell death and proliferation. We now report that κB-Ras proteins act as regulators of NF-κB and Ral pathways, which control inflammation/cell death and
Andrea Oeckinghaus   +9 more
doaj   +1 more source

Signal integration by lipid-mediated spatial cross talk between Ras nanoclusters [PDF]

open access: yes, 2013
Lipid-anchored Ras GTPases form transient, spatially segregated nanoclusters on the plasma membrane that are essential for high-fidelity signal transmission. The lipid composition of Ras nanoclusters however has not previously been investigated.
Abankwa   +65 more
core   +1 more source

The Ins and Outs of RAS Effector Complexes

open access: yesBiomolecules, 2021
RAS oncogenes are among the most commonly mutated proteins in human cancers. They regulate a wide range of effector pathways that control cell proliferation, survival, differentiation, migration and metabolic status.
Christina Kiel   +2 more
doaj   +1 more source

A role for the Ral guanine nucleotide dissociation stimulator in mediating Ras-induced transformation [PDF]

open access: yes, 1996
Oncogenic Ras transforms cells through the activation of multiple downstream pathways mediated by separate effector molecules, one of which is Raf. Here we report the identification of a second ras-binding protein that can induce cellular transformation ...
Camonis, J. H.   +4 more
core   +1 more source

A proteomic atlas of senescence-associated secretomes for aging biomarker development. [PDF]

open access: yes, 2020
The senescence-associated secretory phenotype (SASP) has recently emerged as a driver of and promising therapeutic target for multiple age-related conditions, ranging from neurodegeneration to cancer.
Basisty, Nathan   +11 more
core   +1 more source

PIK3CB and K-ras in oral squamous Cell carcinoma. A possible cross-talk!

open access: yesJournal of Orofacial Sciences, 2014
Background: PIK3 and K-ras are signal transducing proteins involved and mediating many responses related to cell cycle growth regulation. Until date, there has been only limited evidence about the expression of K-ras and PKI3CB in oral squamous cell ...
Natheer H Al-Rawi   +2 more
doaj   +1 more source

Lipid raft microdomain compartmentalization of TC10 is required for insulin signaling and GLUT4 translocation. [PDF]

open access: yes, 2001
Recent studies indicate that insulin stimulation of glucose transporter (GLUT)4 translocation requires at least two distinct insulin receptor-mediated signals: one leading to the activation of phosphatidylinositol 3 (PI-3) kinase and the other to the ...
Chiang, SH   +7 more
core   +3 more sources

Membrane interactions of the globular domain and the hypervariable region of KRAS4b define its unique diffusion behavior

open access: yeseLife, 2020
The RAS proteins are GTP-dependent switches that regulate signaling pathways and are frequently mutated in cancer. RAS proteins concentrate in the plasma membrane via lipid-tethers and hypervariable region side-chain interactions in distinct nano-domains.
Debanjan Goswami   +17 more
doaj   +1 more source

RAS-inhibiting biologics identify and probe druggable pockets including an SII-α3 allosteric site

open access: yesNature Communications, 2021
Oncogenic RAS mutants remain difficult to target with small molecules. Here, the authors show that RAS-binding Affimer proteins inhibit RAS signaling while binding diverse regions on the RAS surface, suggesting the potential to use Affimers as tools to ...
Katarzyna Z. Haza   +20 more
doaj   +1 more source

Analysis of Binding Site Hot Spots on the Surface of Ras GTPase [PDF]

open access: yes, 2011
We have recently discovered an allosteric switch in Ras, bringing an additional level of complexity to this GTPase whose mutants are involved in nearly 30% of cancers.
Buhrman, Greg   +9 more
core   +2 more sources

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