Results 111 to 120 of about 20,458 (226)
Assessment of the effects of the TSC1 Y948N, I954K and L963S variants on TORC1 signaling.
The TSC1 variants were coexpressed in transfected HEK 293T cells with TSC2 and S6K. TSC2, TSC1, S6K and T389-phosphorylated S6K (T389) signals were estimated by immunoblotting.
Marianne Hoogeveen-Westerveld (549062) +7 more
core +1 more source
Flies lacking Akt phosphorylation sites on Tsc1 and Tsc2 are viable and normal in size.
(A) Expression levels of myc-Tsc1 in fly lines homozygous for the Tsc129 mutation, rescued by ubiquitous expression of Tsc1WT, Tsc1S533A or Tsc1S533D, or flies homozygous for both the Tsc129 and Tsc2192 mutations rescued to viability by ubiquitous ...
Aurelio A. Teleman (187510) +1 more
core +1 more source
E. faecalis is enriched in HCC tissue and can promote liver tumourigenesis by activating mTOR signalling pathway. Obg derived from E. faecalis extracellular vesicles (EVs) is a GTPase physically interacts with mTOR, and acts as an interkingdom activator of mTOR. EF‐Obg expression level in HCC tissue correlates with poor prognosis in HCC patients.
Ning Ma +18 more
wiley +1 more source
A 3D bioprinted breast cancer model was created to more accurately reproduce in vivo tumor characteristics compared to conventional 2D cultures. Distinct cell adhesion patterns, reduced mTOR signaling, and altered drug responses were observed under 3D conditions.
Dorottya Moldvai +10 more
wiley +1 more source
Flies lacking Akt phosphorylation sites on both Tsc1 and Tsc2 are slightly lean.
Triglyceride levels normalized to total body protein for Tsc129 homozygotes rescued by ubiquitous expression of Tsc1WT (“WT”), Tsc1S533A (“S533A”) or Tsc1S533D(“S533D”), or flies homozygous for both the Tsc129 and Tsc2192 mutations rescued to viability ...
Aurelio A. Teleman (187510) +1 more
core +1 more source
The role of TSC1 and TSC2 proteins in neuronal axons
Tuberous Sclerosis Complex 1 and 2 proteins, TSC1 and TSC2 respectively, participate in a multiprotein complex with a crucial role for the proper development and function of the nervous system. This complex primarily acts as an inhibitor of the mechanistic target of rapamycin (mTOR) kinase, and mutations in either TSC1 or TSC2 cause a ...
Vasiliki Karalis +3 more
openaire +2 more sources
The Dual Role of Autophagy in Cancer: Mechanisms and Therapeutic Strategies
Autophagy is a conserved cellular process degrading dysfunctional organelles and protein aggregates to maintain cell homeostasis, and it exhibits context‐dependent duality in cancer. Autophagy functions as a critical tumor‐suppressive mechanism by preventing DNA damage and mutation during tumor initiation.
Xiang‐Zheng Gao +4 more
wiley +1 more source
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutations in the TSC1 or TSC2 genes. The TSC1 and TSC2 gene products, TSC1 and TSC2, form a complex that inhibits the mammalian target of rapamycin (mTOR) complex 1 (TORC1 ...
Ekong, Rosemary +67 more
core +1 more source
Background Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem disorder, caused by a loss‐of‐function of either TSC1 or TSC2 gene. However, in 10%–15% TSC patients there is no pathogenic variant identified in either TSC1 or TSC2 genes ...
Seung Woo Ryu +8 more
doaj +1 more source
Oxidative Stress in the Tumor Immune Microenvironment: Mechanisms and Therapeutic Perspectives
Oxidative stress is involved in several key processes in cancer, including redox regulation, DNA damage, post‐translational modifications, transcriptional regulation, epigenetic modifications, metabolic reprogramming, cell death, and immune modulation. These mechanisms collectively influence tumor progression, immune evasion, and therapeutic responses,
Zhen Wang +14 more
wiley +1 more source

