期刊
MOLECULAR AND CELLULAR BIOLOGY
卷 20, 期 24, 页码 9236-9246出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.20.24.9236-9246.2000
关键词
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The r-PTP eta gene encodes a rat receptor-type protein tyrosine phosphatase whose expression is negatively regulated by neoplastic cell transformation, Here we first demonstrate a dramatic reduction in DEP-1/HPTP eta (the human homolog of r-PTP eta) expression in a panel of human thyroid carcinomas. Subsequently, we show that the reexpression of the r-PTP eta gene in highly malignant rat thyroid cells transformed by retroviruses carrying the v-mos and v-ms-Ki oncogenes suppresses their malignant phenotype. Cell cycle analysis demonstrated that r-PTP eta caused G(1) growth arrest and increased the cyclin-dependent kinase inhibitor p27(Kip1) protein level by reducing the proteasome-dependent degradation rate. We propose that the r-PTP eta tumor suppressor activity is mediated by p27(Kip1) protein stabilization, because suppression of p27(Kip1) protein synthesis using p27-specific antisense oligonucleotides blocked the growth-inhibitory effect induced by r-PTP eta, Furthermore, we provide evidence that in v-mos- or v-ras-Ki-transformed thyroid cells, the p27(Kip1) protein level was regulated by the mitogen-activated protein (MAP) kinase pathway and that r-PTP eta regulated p27(Kip1) stability by preventing v-mos- or v-ras-Ki-induced MAP kinase activation.
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