Basic information
Biomarker: PTEN
Histology type: endometrial carcinoma
Cohort characteristics
Country: China.
Region: Hubei
Followed up time :
Subgroup 1 name : Loss of PTEN expression in endometrial hyperplasia
Subgroup 1 number: 4
Subgroup 2 name: PTEN expression in endometrial hyperplasia
Subgroup 2 number: 67
Total number | Group I | Group I number | Group II | Group II number | Group III | Group III number | Group IV | Group IV number |
---|---|---|---|---|---|---|---|---|
200 | EC | 73 | endometrial atypical hyperplasia | 25 | endometrial hyperplasi | 71 | normal endometrium | 31 |
Sample information
Conclusion: Loss of PTEN expression is an early event in endometrial tumorigenesis. Detection of PTEN protein may be a diagnostic biomarker for the earliest endometrial precancers and adenocarcinoma.
Sample type : tissue
Sample method: immunohistochemistry
Expression pattern : Loss expression
Disease information
Related information
Funtion Uniprot: Tumor suppressor. Acts as a dual-specificity protein phosphatase, dephosphorylating tyrosine-, serine- and threonine-phosphorylated proteins. Also acts as a lipid phosphatase, removing the phosphate in the D3 position of the inositol ring from phosphatidylinositol 3,4,5-trisphosphate, phosphatidylinositol 3,4-diphosphate, phosphatidylinositol 3-phosphate and inositol 1,3,4,5-tetrakisphosphate with order of substrate preference in vitro PtdIns(3,4,5)P3 > PtdIns(3,4)P2 > PtdIns3P > Ins(1,3,4,5)P4 (PubMed:26504226, PubMed:16824732). The lipid phosphatase activity is critical for its tumor suppressor function. Antagonizes the PI3K-AKT/PKB signaling pathway by dephosphorylating phosphoinositides and thereby modulating cell cycle progression and cell survival. The unphosphorylated form cooperates with MAGI2 to suppress AKT1 activation. Dephosphorylates tyrosine-phosphorylated focal adhesion kinase and inhibits cell migration and integrin-mediated cell spreading and focal adhesion formation. Plays a role as a key modulator of the AKT-mTOR signaling pathway controlling the tempo of the process of newborn neurons integration during adult neurogenesis, including correct neuron positioning, dendritic development and synapse formation. May be a negative regulator of insulin signaling and glucose metabolism in adipose tissue. The nuclear monoubiquitinated form possesses greater apoptotic potential, whereas the cytoplasmic nonubiquitinated form induces less tumor suppressive ability. In motile cells, suppresses the formation of lateral pseudopods and thereby promotes cell polarization and directed movement.Isoform alpha Functional kinase, like isoform 1 it antagonizes the PI3K-AKT/PKB signaling pathway. Plays a role in mitochondrial energetic metabolism by promoting COX activity and ATP production, via collaboration with isoform 1 in increasing protein levels of PINK1.
UniProt ID: P60484
UniProt Link: https://www.uniprot.org/uniprotkb/P60484/entry
Biological function from UniProt: #Apoptosis #Lipid metabolism #Neurogenesis
Molecular function from UniProt:
Tissue specificity from UniProt: Expressed at a relatively high level in all adult tissues, including heart, brain, placenta, lung, liver, muscle, kidney and pancreas.
Subcellular UniProt: #Cytoplasm #Nucleus #Secreted
Alternative name from UniProt:
Catalytic activity: a 1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol-3,4,5-trisphosphate) + H2O = a 1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol-4,5-bisphosphate) + phosphate. $ H2O + O-phospho-L-seryl-[protein] = L-seryl-[protein] + phosphate$ H2O + O-phospho-L-threonyl-[protein] = L-threonyl-[protein] + phosphate $ H2O + O-phospho-L-tyrosyl-[protein] = L-tyrosyl-[protein] + phosphate $ 1,2-dioctanoyl-sn-glycero-3-phospho-(1D-myo-inositol-3,4,5-trisphosphate) + H2O = 1,2-dioctanoyl-sn-glycero-3-phospho-(1D-myo-inositol-4,5-bisphosphate) + phosphate $1,2-dihexadecanoyl-sn-glycero-3-phospho-(1D-myo-inositol-3,4,5-trisphosphate) + H2O = 1,2-dihexadecanoyl-sn-glycero-3-phospho-(1D-myo-inositol-4,5-bisphosphate) + phosphate
Activity regulation: Enzymatic activity is enhanced in the presence of phosphatidylserine.
Recommended name: Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN
Gene name from HGNC: PTEN (BZS, MHAM, MMAC1, PTEN1, TEP1)
HPA class: Cancer-related genes Disease related genes Enzymes Human disease related genes Metabolic proteins Potential drug targets Transcription factors
AlphaFold DB: P60484
AlphaFold Link: https://alphafold.ebi.ac.uk/entry/P60484
Induction: Down-regulated by TGFB1.
HPA link: https://www.proteinatlas.org/ENSG00000171862-PTEN
Tissue specificity RNA from HPA: Low tissue specificity
Tissue expression from HPA: Cytoplasmic expression in most tissues.
Single cell type specificity Low cell type specificity
Immune cell specificity: Immune cell enhanced (neutrophil)
Subcellular summary HPA Located in Nucleoplasm, Cytosol
Cancer prognostic summary HPA Prognostic marker in renal cancer (unfavorable)
Pathology link: https://www.proteinatlas.org/ENSG00000171862-PTEN/pathology
Pathology endo: https://www.proteinatlas.org/ENSG00000171862-PTEN/pathology/endometrial+cancer
Phenotype ID: 158350$ 158350$ 275355 $608089$ 613028$ 176807$ 605309
Disease: Cowden syndrome 1 (CWS1)$ Lhermitte-Duclos disease (LDD)$ Squamous cell carcinoma of the head and neck (HNSCC)$ Endometrial cancer (ENDMC)$ No disease ID$ Glioma 2 (GLM2)$Prostate cancer (PC) $Macrocephaly/autism syndrome (MCEPHAS)$ No disease ID$
Note1: The disease is caused by variants affecting the gene represented in this entry
OMIM: 601728
OMIM link1: https://www.omim.org/entry/158350$ https://www.omim.org/entry/158350$ https://www.omim.org/entry/275355$ https://www.omim.org/entry/608089$ $ https://www.omim.org/entry/613028$ https://www.omim.org/entry/176807$ https://www.omim.org/entry/605309 $
OMIM link2: https://www.omim.org/entry/601728
HGNC ID: HGNC:9588
HGNC link: https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:9588