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1.
Biochim Biophys Acta Gene Regul Mech ; 1862(6): 657-669, 2019 06.
Article in English | MEDLINE | ID: mdl-31075539

ABSTRACT

Variation in Disrupted-in-Schizophrenia 1 (DISC1) increases the risk for neurodegenerative diseases, schizophrenia, and other mental disorders. However, the functions of DISC1 associated with the development of these diseases remain unclear. DISC1 has been reported to inhibit Akt/mTORC1 signaling, a major regulator of translation, and recent studies indicate that DISC1 could exert a direct role in translational regulation. Here, we present evidence of a novel role of DISC1 in the maintenance of protein synthesis during oxidative stress. In order to investigate DISC1 function independently of Akt/mTORC1, we used Tsc2-/- cells, where mTORC1 activation is independent of Akt. DISC1 knockdown enhanced inhibition of protein synthesis in cells treated with sodium arsenite (SA), an oxidative agent used for studying stress granules (SGs) dynamics and translational control. N-acetyl-cysteine inhibited the effect of DISC1, suggesting that DISC1 affects translation in response to oxidative stress. DISC1 decreased SGs number in SA-treated cells, but resided outside SGs and maintained protein synthesis independently of a proper SG nucleation. DISC1-dependent stimulation of translation in SA-treated cells was supported by its interaction with eIF3h, a component of the canonical translation initiation machinery. Consistent with a role in the homeostatic maintenance of translation, DISC1 knockdown or overexpression decreased cell viability after SA exposure. Our data suggest that DISC1 is a relevant component of the cellular response to stress, maintaining certain levels of translation and preserving cell integrity. This novel function of DISC1 might be involved in its association with pathologies affecting tissues frequently exposed to oxidative stress.


Subject(s)
Arsenites/pharmacology , Nerve Tissue Proteins/metabolism , Oxidative Stress/drug effects , Sodium Compounds/pharmacology , Animals , Cell Survival/drug effects , Cytoplasmic Granules/metabolism , DNA Helicases/metabolism , Eukaryotic Initiation Factor-3/metabolism , Gene Expression Regulation , Gene Knockdown Techniques , HEK293 Cells , Humans , Mechanistic Target of Rapamycin Complex 1 , Mice , Nerve Tissue Proteins/genetics , Oncogene Protein v-akt , Poly-ADP-Ribose Binding Proteins/metabolism , RNA Helicases/metabolism , RNA Recognition Motif Proteins/metabolism , Transcriptome , Tuberous Sclerosis Complex 2 Protein/genetics
2.
Int J Cancer ; 138(8): 1815-23, 2016 Apr 15.
Article in English | MEDLINE | ID: mdl-26234902

ABSTRACT

Rheb is a conserved small GTPase that belongs to the Ras superfamily, and is mainly involved in activation of cell growth through stimulation of mTORC1 activity. Because deregulation of the Rheb/mTORC1 signaling is associated with proliferative disorders and cancer, inhibition of mTORC1 has been therapeutically approached. Although this therapy has proven antitumor activity, its efficacy is not as expected. Here, we will review the main work on the identification of the role of Rheb in cell growth, and on the relevance of Rheb in proliferative disorders, including cancer. We will also review the Rheb functions that could explain tumor resistance to therapies with mTORC1 inhibitors, and will mainly focus our discussion on mTORC1-independent Rheb functions that could also be implicated in cancer cell survival and tumorigenesis. The current progress on the understanding of the noncanonical Rheb functions prompts future studies to establish their relevance in cancer and in the context of current cancer therapies.


Subject(s)
Carcinogenesis/metabolism , Monomeric GTP-Binding Proteins/physiology , Multiprotein Complexes/physiology , Neuropeptides/physiology , Signal Transduction/physiology , TOR Serine-Threonine Kinases/physiology , Animals , Humans , Mechanistic Target of Rapamycin Complex 1 , Ras Homolog Enriched in Brain Protein
3.
J Cell Biochem ; 113(4): 1253-64, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22121046

ABSTRACT

Constitutive activation of M-Ras has previously been reported to cause morphologic and growth transformation of murine cells, suggesting that M-Ras plays a role in tumorigenesis. Cell transformation by M-Ras correlated with weak activation of the Raf/MEK/ERK pathway, although contributions from other downstream effectors were suggested. Recent studies indicate that signaling events distinct from the Raf/MEK/ERK cascade are critical for human tumorigenesis. However, it is unknown what signaling events M-Ras triggers in human cells. Using constitutively active M-Ras (Q71L) containing additional mutations within its effector-binding loop, we found that M-Ras induces MEK/ERK-dependent and -independent Elk1 activation as well as phosphatidylinositol 3 kinase (PI3K)/Akt and JNK/cJun activation in human MCF-7 breast cancer cells. Among several human cell lines examined, M-Ras-induced MEK/ERK-independent Elk1 activation was only detected in MCF-7 cells, and correlated with Rlf/M-Ras interaction and Ral/JNK activation. Supporting a role for M-Ras signaling in breast cancer, EGF activated M-Ras and promoted its interaction with endogenous Rlf. In addition, constitutive activation of M-Ras induced estrogen-independent growth of MCF-7 cells that was dependent on PI3K/Akt, MEK/ERK, and JNK activation. Thus, our studies demonstrate that M-Ras signaling activity differs between human cells, highlighting the importance of defining Ras protein signaling within each cell type, especially when designing treatments for Ras-induced cancer. These findings also demonstrate that M-Ras activity may be important for progression of EGFR-dependent tumors.


Subject(s)
Gene Expression Regulation, Enzymologic , MAP Kinase Kinase 4/metabolism , Mitogen-Activated Protein Kinases/metabolism , Monomeric GTP-Binding Proteins/physiology , ral GTP-Binding Proteins/metabolism , Cell Line, Tumor , Enzyme Activation , Female , Humans , Immunoprecipitation , Signal Transduction
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