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. 2020 Jul 18;9(7):1725. doi: 10.3390/cells9071725

Table 1.

List of PTEN alteration, observable effects, and experimental models.

Type of Cancer PTEN Alteration Observable Effects Models References
Thyroid PTEN loss Down-regulation of Krebs cycle and OXPHOS gene expression, defective mitochondria, reduced respiration and compensatory glycolysis. PTEN-deficient mouse model [18]
Liver PTEN Knockdown Increased oxidative stress levels, increase of reactive oxygen species (ROS), elevated genomic damage PTEN deficient mice maintained with a high fat diet [19]
Glioblastoma Ectopic expression of WT PTEN and mutants Effects on autophagic flux and lysosomal mass. U87MG human glioma cells [20]
Hepatocellular carcinoma PTEN loss Suppression of autophagy at the formation and maturation steps of autophagosomes Hepatocyte-specific PTEN-deficient mice [21]
Breast cancer Up-regulation of PTEN Induction of autophagy and reduction of breast cancer cell growth Hormone dependent breast cancer cells [15]
Melanoma PTEN loss Induction of immunosuppressive cytokines, reduction of T-cells infiltration in tumor tissue, inhibition of autophagy and T cell–mediated cell death PTEN- deficient melanoma mouse models [22]
Melanoma Cre-inactivated allele of PTEN Repression of a protective immune response in the tumor microenvironment, increase in tumor growth and metastasis BRAF V600E/PTEN loss murine melanoma models [23]
Prostate PTEN Knockdown Induction of tumor microenvironment remodeling, associated with immunosuppressive infrastructure PTEN conditional knockout mice [24]
Glioblastoma PTEN Knockdown or PTEN mutation Infiltration of macrophage that secrete factors promoting glioma cell survival and angiogenesis. PTEN null glioma mouse models [25]
Liver PTEN Knockdown Spontaneous development and progression of liver tumors from progenitor cells. Induction of hepatic microenvironment remodeling. PTEN-null liver mouse models [9]
Lung PTEN silencing targeting human PTEN Reduction of IFN—induced inflammatory response, cell growth inhibition, and cytotoxicity A549 and PC14PE6/AS2 human lung adenocarcinoma cells [26]