Human Prostrate Cancer Hallmarks Map

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Prostrate Cancer Epithelial Mesenchymal Transition(EMT)

Intrinsic components of Prostrate Cancer Epithelial Mesenchymal Transition(EMT)

ProteinProtein NameMolecular TypeEvidenceReference
MYCV-myc avian myelocytomatosis viral oncogene homologTranscription Factorc-MYC is involved in prostate cancer epithelial mesenchymal transition upon phosphorylation by ERK2.Reference
TP53Tumor protein p53Transcription FactorTP53 loss in prostate epithelial cell results in epithelial mesenchymal transition in prostate cancer.Reference
SMAD4SMAD family member 4Transcription FactorSMAD4 is involved in prostate cancer epithelial mesenchymal transition through TGFbeta/BMP-SMAD4 signaling pathway.Reference
WT1Wilms tumor 1Transcription FactorWilm's tumour gene (WT1) play an important role in the epithelial mesenchymal transition in PC-3 prostate cancer cell.Reference
TGFBR2Transforming growth factor, beta receptor IIReceptor Serine/threonine KinaseIncreased production of TGF beta causes epithelial mesenchymal transitionReference
TGFBR2Transforming growth factor, beta receptor IIReceptor Serine/threonine KinaseIncreased production of TGF beta causes epithelial mesenchymal transitionReference
AXLAXL receptor tyrosine kinaseReceptor Tyrosine KinaseAXL regulates epithelial mesenchymal (EMT) marker expression in prostate cancer, supported by experiments on PC3 and DU145 prostate cancer cells.Reference
EGFREpidermal growth factor receptorReceptor Tyrosine KinaseEGFR is involved in prostate cancer epithelial mesenchymal transition in a LIV-1 induced and ERK mediated signaling.Reference
FGFR1Fibroblast growth factor receptor 1Receptor Tyrosine KinaseFGFR1 activation results in epithelial mesenchymal transition in the epithelial compartment during prostate cancer progression.Reference
ARAndrogen receptorNuclear ReceptorAndrogen receptor mediated signaling is responsible for epithelial mesenchymal transition in prostate epithelial cellsReference
ARAndrogen receptorNuclear ReceptorAndrogen receptor mediated signaling is responsible for epithelial mesenchymal transition in prostate epithelial cellsReference
CTNNB1Catenin (cadherin-associated protein), beta 1, 88kDaAdhesion MoleculeBeta catenine is associated with epithelial mesenchymal transition in prostate cancer development mediated by SOX2.Reference
CTNNB1Catenin (cadherin-associated protein), beta 1, 88kDaAdhesion MoleculeBeta catenine is involved in the epithelial mesenchymal transition of prostate cancer stem cell through HIF-1alpha/beta-catenin-dependent signaling pathway.Reference
EGFREpidermal growth factor receptorReceptor Tyrosine KinaseSPINK1, which is overexpressed in prostate cancer promotes EMT through EGFR signaling.Reference
ARAndrogen receptorNuclear ReceptorIt promotes prostate cancer metastasis by regulating EMT.Reference
ARAndrogen receptorNuclear ReceptorAndrogen deprivation therapy mediates prostate cancer EMT through a feed back loop involving AR and Zeb1 transcription factor.Reference
TP53Tumor protein p53Transcription FactorLoss of TP53 enhances EMT and stemness of prostate cancer cells through partially through repressing miR-145.Reference
CTNNB1Catenin (cadherin-associated protein), beta 1, 88kDaAdhesion MoleculeEPLIN downregulation in metastatic prostate cancer results in the activation of beta catenine mediated pro-EMT gene expression.Reference
JAK2Janus kinase 2Tyrosine KinaseJAK2-STAT5a/b mediated signaling plays a role in prostate cancer epithelial mesenchymal transition.Reference
DAB2IPDAB2 interacting proteinRas GTPase-activating proteinLoss of DAB2IP is associated with prostate cancer epithelial mesenchymal transition , supported by experiments on human prostate xenograft-mouse model.Reference
PMLPromyelocytic leukemiaTranscription Regulatory ProteinCytoplasmic promyelocytic leukaemia (cPML) plays a very critical role in the induction of prostate cancer associated epithelial mesenchymal transition (EMT) through activation of TGF beta mediated signaling.Reference
TWIST1Twist family bHLH transcription factor 1Transcription FactorTWIST1 transcription factor plays a vital role in human prostate cancer associated epithelial mesenchymal transition through interaction with androgen receptor(AR) and there by promotes castration resistance.Reference
POSTNPeriostin, osteoblast specific factorAdhesion MoleculePeriostin(POSTN), which is upregulated in human prostate cancer plays a role in prostate cancer related epithelial mesenchymal transition (EMT) in a TGF beta dependent manner.Reference
CFDComplement factor D (adipsin)EnzymeAdiponectin (CFD), a hormone secreted by adipose tissue and frequently inactivated in human prostate cancer, plays a tumour suppressive role in the context of prostate cancer associated epithelial mesenchymal transition.Reference
PAK1p21 protein (Cdc42/Rac)-activated kinase 1Serine/Threonine KinaseP21-activated kinase1 (PAK1) plays a role in prostate cancer epithelial mesenchymal transition through a TGF-Beta deependent signaling pathway.Reference
PARP1Poly(ADP-ribose) polymerase 1EnzymePoly (ADP-ribose) polymerase (PARP) is involved in the promotion of prostate cancer associated epithelial mesenchymal transition (EMT) ina TGF beta responsive manner.Reference
FGF19Fibroblast growth factor 19Growth FactorFGF19, highly expressed in human prostate cancer, plays a role in prostate cancer associated epithelial mesenchymal transition (EMT).Reference
PIWIL2Piwi-like RNA-mediated gene silencing 2Transcription Regulatory ProteinPiwi-like RNA-mediated gene silencing 2 (Piwil2), an oncogene which is upregulated in human prostate cancer, plays a significant role in modulation of prostate cancer associated epithelial mesenchymal transition (EMT) through regulation of MMP9 expression.Reference
EPLINLIM domain and actin binding 1Cytoskeletal ProteinEPLIN, an actin associated molecule, plays a pivotal role in regulation of prostate cancer associated epithelial mesenchymal transition (EMT).Reference
LCN2Lipocalin 2Transport/Cargo ProteinLipocalin 2 (LCN2), a member of the lipocalin family, is highly expressed in human prostate cancer and is involved in the induction of prostate cancer associated epithelial mesenchymal transition (EMT) through regulation of SLUG expression via ERK pathway activation.Reference