4.5 Article Retracted Publication

被撤回的出版物: Rat protein tyrosine phosphatase η suppresses the neoplastic phenotype of retrovirally transformed thyroid cells through the stabilization of p27Kip1 (Retracted article. See vol. 38, 2018)

Journal

MOLECULAR AND CELLULAR BIOLOGY
Volume 20, Issue 24, Pages 9236-9246

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.20.24.9236-9246.2000

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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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