In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS)
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Title
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS)
Authors
Keywords
PI3K/AKT/mTOR pathway, PI3K/AKT/mTOR inhibitors, PIK3CA mutations, Rapamycin, Wortmannin, Mosaic neurocutaneous disorders, PROS, Target therapy
Journal
NEUROGENETICS
Volume 19, Issue 2, Pages 77-91
Publisher
Springer Nature
Online
2018-03-16
DOI
10.1007/s10048-018-0540-1
References
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Related references
Note: Only part of the references are listed.- Phenotypic heterogeneity inPIK3CA-related overgrowth spectrum
- (2016) H. Vahidnezhad et al. BRITISH JOURNAL OF DERMATOLOGY
- CLOVES syndrome: review of a PIK3CA-related overgrowth spectrum (PROS)
- (2016) A. Martinez-Lopez et al. CLINICAL GENETICS
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- (2016) Hassan Vahidnezhad et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Somatic Activating PIK3CA Mutations Cause Venous Malformation
- (2015) Nisha Limaye et al. AMERICAN JOURNAL OF HUMAN GENETICS
- PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia
- (2015) Laura A. Jansen et al. BRAIN
- Klippel-Trenaunay syndrome belongs to thePIK3CA-related overgrowth spectrum (PROS)
- (2015) Hassan Vahidnezhad et al. EXPERIMENTAL DERMATOLOGY
- Akt inhibitors in cancer treatment: The long journey from drug discovery to clinical use (Review)
- (2015) GEORGE MIHAI NITULESCU et al. INTERNATIONAL JOURNAL OF ONCOLOGY
- Lymphatic and Other Vascular Malformative/Overgrowth Disorders Are Caused by Somatic Mutations in PIK3CA
- (2015) Valerie L. Luks et al. JOURNAL OF PEDIATRICS
- Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors
- (2015) Daria C. Loconte et al. PLoS One
- Mosaic Neurocutaneous Disorders and Their Causes
- (2015) Martino Ruggieri et al. Seminars in Pediatric Neurology
- Repression of AKT signaling by ARQ 092 in cells and tissues from patients with Proteus syndrome
- (2015) Marjorie J. Lindhurst et al. Scientific Reports
- Targeting AKT1-E17K and the PI3K/AKT Pathway with an Allosteric AKT Inhibitor, ARQ 092
- (2015) Yi Yu et al. PLoS One
- PIK3CA-related overgrowth spectrum (PROS): Diagnostic and testing eligibility criteria, differential diagnosis, and evaluation
- (2014) Kim M. Keppler-Noreuil et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Clinical delineation and natural history of thePIK3CA-related overgrowth spectrum
- (2014) Kim M. Keppler-Noreuil et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- PI3K and cancer: lessons, challenges and opportunities
- (2014) David A. Fruman et al. NATURE REVIEWS DRUG DISCOVERY
- PIK3CA Activating Mutations in Facial Infiltrating Lipomatosis
- (2013) Reid A. Maclellan et al. PLASTIC AND RECONSTRUCTIVE SURGERY
- Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome
- (2012) Kyle C. Kurek et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Germline PIK3CA and AKT1 Mutations in Cowden and Cowden-like Syndromes
- (2012) Mohammed S. Orloff et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Akt is efficiently activated by PIF-pocket- and PtdIns(3,4,5)P3-dependent mechanisms leading to resistance to PDK1 inhibitors
- (2012) Ayaz Najafov et al. BIOCHEMICAL JOURNAL
- Somatic gain-of-function mutations in PIK3CA in patients with macrodactyly
- (2012) Jonathan J. Rios et al. HUMAN MOLECULAR GENETICS
- Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA
- (2012) Marjorie J Lindhurst et al. NATURE GENETICS
- De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
- (2012) Jean-Baptiste Rivière et al. NATURE GENETICS
- De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly
- (2012) Jeong Ho Lee et al. NATURE GENETICS
- Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations
- (2012) Annapurna Poduri et al. NEURON
- A Mosaic Activating Mutation inAKT1Associated with the Proteus Syndrome
- (2011) Marjorie J. Lindhurst et al. NEW ENGLAND JOURNAL OF MEDICINE
- An Activating Mutation of AKT2 and Human Hypoglycemia
- (2011) K. Hussain et al. SCIENCE
- Targeting the phosphoinositide 3-kinase pathway in cancer
- (2009) Pixu Liu et al. NATURE REVIEWS DRUG DISCOVERY
- Molecular Mechanism of an Oncogenic Mutation That Alters Membrane Targeting: Glu17Lys Modifies the PIP Lipid Specificity of the AKT1 PH Domain†
- (2008) Kyle E. Landgraf et al. BIOCHEMISTRY
- PI3K pathway alterations in cancer: variations on a theme
- (2008) T L Yuan et al. ONCOGENE
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