Abstract

Mapping of homozygous deletions on human chromosome 10q23 has led to the isolation of a candidate tumor suppressor gene, PTEN , that appears to be mutated at considerable frequency in human cancers. In preliminary screens, mutations of PTEN were detected in 31% (13/42) of glioblastoma cell lines and xenografts, 100% (4/4) of prostate cancer cell lines, 6% (4/65) of breast cancer cell lines and xenografts, and 17% (3/18) of primary glioblastomas. The predicted PTEN product has a protein tyrosine phosphatase domain and extensive homology to tensin, a protein that interacts with actin filaments at focal adhesions. These homologies suggest that PTEN may suppress tumor cell growth by antagonizing protein tyrosine kinases and may regulate tumor cell invasion and metastasis through interactions at focal adhesions.

Keywords

PTENTensinCancer researchProtein tyrosine phosphataseBiologyTumor suppressor geneMetastasisProstate cancerPTPN11Gene productCancerGeneMutationCarcinogenesisKinaseSignal transductionPI3K/AKT/mTOR pathwayCell biologyGeneticsGene expression

MeSH Terms

Amino Acid SequenceBrain NeoplasmsBreast NeoplasmsChromosome MappingChromosomesHumanPair 10FemaleFrameshift MutationGenesTumor SuppressorGlioblastomaHumansMaleMicrofilament ProteinsMolecular Sequence DataMutationNeoplasm TransplantationNeoplasmsPTEN PhosphohydrolasePhosphoric Monoester HydrolasesPhosphotyrosineProstatic NeoplasmsProtein Tyrosine PhosphatasesProtein-Tyrosine KinasesSequence DeletionSequence HomologyAmino AcidTensinsTransplantationHeterologousTumor CellsCulturedTumor Suppressor Proteins

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Publication Info

Year
1997
Type
article
Volume
275
Issue
5308
Pages
1943-1947
Citations
4788
Access
Closed

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Citation Metrics

4788
OpenAlex
196
Influential
3858
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Cite This

Jing Li, Clifford Yen, Danny Liaw et al. (1997). <i>PTEN</i> , a Putative Protein Tyrosine Phosphatase Gene Mutated in Human Brain, Breast, and Prostate Cancer. Science , 275 (5308) , 1943-1947. https://doi.org/10.1126/science.275.5308.1943

Identifiers

DOI
10.1126/science.275.5308.1943
PMID
9072974

Data Quality

Data completeness: 81%