mTOR in Human Diseases

The mechanistic target of rapamycin (mTOR) is a major signaling intermediary that coordinates favorable environmental conditions with cell growth. Indeed, as part of two functionally distinct protein complexes, named mTORC1 and mTORC2, mTOR regulates a variety of cellular processes, including protei...

Description complète

Enregistré dans:
Détails bibliographiques
Auteur principal: Dormond, Olivier
Format: Online
Langue:anglais
Publié: MDPI - Multidisciplinary Digital Publishing Institute 2021
Sujets:
Accès en ligne:33689
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
_version_ 1869518000459087872
author Dormond, Olivier
author_browse Dormond, Olivier
author_facet Dormond, Olivier
author_sort Dormond, Olivier
collection Directory of Open Access Books
description The mechanistic target of rapamycin (mTOR) is a major signaling intermediary that coordinates favorable environmental conditions with cell growth. Indeed, as part of two functionally distinct protein complexes, named mTORC1 and mTORC2, mTOR regulates a variety of cellular processes, including protein, lipid, and nucleotide synthesis, as well as autophagy. Over the last two decades, major molecular advances have been made in mTOR signaling and have revealed the complexity of the events implicated in mTOR function and regulation. In parallel, the role of mTOR in diverse pathological conditions has also been identified, including in cancer, hamartoma, neurological, and metabolic diseases. Through a series of articles, this book focuses on the role played by mTOR in cellular processes, metabolism in particular, and highlights a panel of human diseases for which mTOR inhibition provides or might provide benefits. It also addresses future studies needed to further characterize the role of mTOR in selected disorders, which will help design novel therapeutic approaches. It is therefore intended for everyone who has an interest in mTOR biology and its application in human pathologies.
format Online
id doab-20.500.12854ir-54029
institution Directory of Open Access Books
language eng
publishDate 2021
publishDateRange 2021
publishDateSort 2021
publisher MDPI - Multidisciplinary Digital Publishing Institute
publisherStr MDPI - Multidisciplinary Digital Publishing Institute
record_format ojs
spelling doab-20.500.12854ir-540292024-03-30T23:22:13Z mTOR in Human Diseases Dormond, Olivier R5-920 n/a primary cilia neurodegeneration nutrient sensor PI3K transcriptomics phosphorylation metabolic reprogramming autophagy Alzheimer’s disease rapalogs liver angiogenesis mTOR complex MBSCs advanced biliary tract cancers Medulloblastoma epithelial to mesenchymal transition AMPK p70S6K lipid metabolism thyroid cancer sodium iodide symporter (NIS)/SLC5A5 male fertility anesthesia illumina mTOR inhibitor miRNA Hutchinson-Gilford progeria syndrome (HGPS) eIFs Emery-Dreifuss muscular dystrophy (EDMD) glucose AKT oral cavity squamous cell carcinoma (OSCC) glucose and lipid metabolism cellular signaling aging tumor microenvironment rapamycin leukemia chloral hydrate rapalogues schizophrenia T-cell acute lymphoblastic leukemia senescence lamin A/C neurotoxicity neurodevelopment inhibitor methamphetamine pulmonary fibrosis mTOR mTOR inhibitors combination therapy proteolysis fluid shear stress tumour cachexia biomarkers synapse gluconeogenesis mTOR signal pathway Sertoli cells immunosenescence miRNome protein aggregation senolytics metabolism NGS mTORC2 mTORC1 metabolic diseases IonTorrent apoptosis dopamine receptor nocodazole microenvironment everolimus acute myeloid leukemia immunotherapy spermatogenesis bone remodeling signalling targeted therapy ageing therapy NVP-BEZ235 fructose physical activity laminopathies MC3T3-E1 cells cell signaling microRNA cancer lipolysis melatonin Parkinson’s disease thema EDItEUR::M Medicine and Nursing The mechanistic target of rapamycin (mTOR) is a major signaling intermediary that coordinates favorable environmental conditions with cell growth. Indeed, as part of two functionally distinct protein complexes, named mTORC1 and mTORC2, mTOR regulates a variety of cellular processes, including protein, lipid, and nucleotide synthesis, as well as autophagy. Over the last two decades, major molecular advances have been made in mTOR signaling and have revealed the complexity of the events implicated in mTOR function and regulation. In parallel, the role of mTOR in diverse pathological conditions has also been identified, including in cancer, hamartoma, neurological, and metabolic diseases. Through a series of articles, this book focuses on the role played by mTOR in cellular processes, metabolism in particular, and highlights a panel of human diseases for which mTOR inhibition provides or might provide benefits. It also addresses future studies needed to further characterize the role of mTOR in selected disorders, which will help design novel therapeutic approaches. It is therefore intended for everyone who has an interest in mTOR biology and its application in human pathologies. 2021-02-11T20:17:42Z 2021-02-11T20:17:42Z 2019-06-26 08:44:06 2019 book 33689 9783039210619 9783039210602 https://directory.doabooks.org/handle/20.500.12854/54029 eng image/jpeg Attribution-NonCommercial-NoDerivatives 4.0 International https://mdpi.com/books/pdfview/book/1355 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-03921-061-9 10.3390/books978-3-03921-061-9 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783039210619 9783039210602 480 open access
spellingShingle R5-920
n/a
primary cilia
neurodegeneration
nutrient sensor
PI3K
transcriptomics
phosphorylation
metabolic reprogramming
autophagy
Alzheimer’s disease
rapalogs
liver
angiogenesis
mTOR complex
MBSCs
advanced biliary tract cancers
Medulloblastoma
epithelial to mesenchymal transition
AMPK
p70S6K
lipid metabolism
thyroid cancer
sodium iodide symporter (NIS)/SLC5A5
male fertility
anesthesia
illumina
mTOR inhibitor
miRNA
Hutchinson-Gilford progeria syndrome (HGPS)
eIFs
Emery-Dreifuss muscular dystrophy (EDMD)
glucose
AKT
oral cavity squamous cell carcinoma (OSCC)
glucose and lipid metabolism
cellular signaling
aging
tumor microenvironment
rapamycin
leukemia
chloral hydrate
rapalogues
schizophrenia
T-cell acute lymphoblastic leukemia
senescence
lamin A/C
neurotoxicity
neurodevelopment
inhibitor
methamphetamine
pulmonary fibrosis
mTOR
mTOR inhibitors
combination therapy
proteolysis
fluid shear stress
tumour cachexia
biomarkers
synapse
gluconeogenesis
mTOR signal pathway
Sertoli cells
immunosenescence
miRNome
protein aggregation
senolytics
metabolism
NGS
mTORC2
mTORC1
metabolic diseases
IonTorrent
apoptosis
dopamine receptor
nocodazole
microenvironment
everolimus
acute myeloid leukemia
immunotherapy
spermatogenesis
bone remodeling
signalling
targeted therapy
ageing
therapy
NVP-BEZ235
fructose
physical activity
laminopathies
MC3T3-E1 cells
cell signaling
microRNA
cancer
lipolysis
melatonin
Parkinson’s disease
thema EDItEUR::M Medicine and Nursing
Dormond, Olivier
mTOR in Human Diseases
title mTOR in Human Diseases
title_full mTOR in Human Diseases
title_fullStr mTOR in Human Diseases
title_full_unstemmed mTOR in Human Diseases
title_short mTOR in Human Diseases
title_sort mtor in human diseases
topic R5-920
n/a
primary cilia
neurodegeneration
nutrient sensor
PI3K
transcriptomics
phosphorylation
metabolic reprogramming
autophagy
Alzheimer’s disease
rapalogs
liver
angiogenesis
mTOR complex
MBSCs
advanced biliary tract cancers
Medulloblastoma
epithelial to mesenchymal transition
AMPK
p70S6K
lipid metabolism
thyroid cancer
sodium iodide symporter (NIS)/SLC5A5
male fertility
anesthesia
illumina
mTOR inhibitor
miRNA
Hutchinson-Gilford progeria syndrome (HGPS)
eIFs
Emery-Dreifuss muscular dystrophy (EDMD)
glucose
AKT
oral cavity squamous cell carcinoma (OSCC)
glucose and lipid metabolism
cellular signaling
aging
tumor microenvironment
rapamycin
leukemia
chloral hydrate
rapalogues
schizophrenia
T-cell acute lymphoblastic leukemia
senescence
lamin A/C
neurotoxicity
neurodevelopment
inhibitor
methamphetamine
pulmonary fibrosis
mTOR
mTOR inhibitors
combination therapy
proteolysis
fluid shear stress
tumour cachexia
biomarkers
synapse
gluconeogenesis
mTOR signal pathway
Sertoli cells
immunosenescence
miRNome
protein aggregation
senolytics
metabolism
NGS
mTORC2
mTORC1
metabolic diseases
IonTorrent
apoptosis
dopamine receptor
nocodazole
microenvironment
everolimus
acute myeloid leukemia
immunotherapy
spermatogenesis
bone remodeling
signalling
targeted therapy
ageing
therapy
NVP-BEZ235
fructose
physical activity
laminopathies
MC3T3-E1 cells
cell signaling
microRNA
cancer
lipolysis
melatonin
Parkinson’s disease
thema EDItEUR::M Medicine and Nursing
topic_facet R5-920
n/a
primary cilia
neurodegeneration
nutrient sensor
PI3K
transcriptomics
phosphorylation
metabolic reprogramming
autophagy
Alzheimer’s disease
rapalogs
liver
angiogenesis
mTOR complex
MBSCs
advanced biliary tract cancers
Medulloblastoma
epithelial to mesenchymal transition
AMPK
p70S6K
lipid metabolism
thyroid cancer
sodium iodide symporter (NIS)/SLC5A5
male fertility
anesthesia
illumina
mTOR inhibitor
miRNA
Hutchinson-Gilford progeria syndrome (HGPS)
eIFs
Emery-Dreifuss muscular dystrophy (EDMD)
glucose
AKT
oral cavity squamous cell carcinoma (OSCC)
glucose and lipid metabolism
cellular signaling
aging
tumor microenvironment
rapamycin
leukemia
chloral hydrate
rapalogues
schizophrenia
T-cell acute lymphoblastic leukemia
senescence
lamin A/C
neurotoxicity
neurodevelopment
inhibitor
methamphetamine
pulmonary fibrosis
mTOR
mTOR inhibitors
combination therapy
proteolysis
fluid shear stress
tumour cachexia
biomarkers
synapse
gluconeogenesis
mTOR signal pathway
Sertoli cells
immunosenescence
miRNome
protein aggregation
senolytics
metabolism
NGS
mTORC2
mTORC1
metabolic diseases
IonTorrent
apoptosis
dopamine receptor
nocodazole
microenvironment
everolimus
acute myeloid leukemia
immunotherapy
spermatogenesis
bone remodeling
signalling
targeted therapy
ageing
therapy
NVP-BEZ235
fructose
physical activity
laminopathies
MC3T3-E1 cells
cell signaling
microRNA
cancer
lipolysis
melatonin
Parkinson’s disease
thema EDItEUR::M Medicine and Nursing
url 33689
work_keys_str_mv AT dormondolivier mtorinhumandiseases