Literature DB >> 11179477

Mutation of the PTEN gene in advanced cervical cancer correlated with tumor progression and poor outcome after radiotherapy.

Y Harima1, S Sawada, K Nagata, M Sougawa, V Ostapenko, T Ohnishi.   

Abstract

Improvement in management of advanced cervical cancer after radiotherapy requires a better understanding of its biological behavior. PTEN/MMAC/TEP(PTEN), a candidate tumor suppressor gene located at chromosome 10q23.3, was recently identified and found to be frequently mutated in several different types of human tumors. In contrast, rare mutations of the PTEN gene have been reported in cervical cancer. The aim of this study was to determine whether mutation of PTEN leads to increased genomic alteration in advanced cervical carcinoma, and to identify the correlation between mutation of PTEN and patient outcome after radiotherapy. We examined 50 primary advanced cervical carcinomas (37 patients of Stage IIIB, 13 patients of Stage IVA) treated with definitive radiotherapy using a PCR-based assay followed by SSCP and direct sequencing. The PTEN gene was mutated in 8 of the 50 (16%) patients (2 of Stage III, and 6 of Stage IV). There was a significant difference in Stage III versus IV between the wild-type PTEN patients and mutant PTEN patients (P=0.002). The tumor size was 6+/-2.1 cm in the wild-type PTEN tumors versus 8.5+/-2 cm in the mutant PTEN tumors (P=0.009). In addition, there was a significant difference in survival between the wild-type PTEN patients and mutant PTEN patients (P=0.009). The results of this study suggest that the PTEN gene mutation rate increases with tumor progression, and that the PTEN gene may play a role in both progression of cervical carcinoma and treatment outcome.

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Year:  2001        PMID: 11179477     DOI: 10.3892/ijo.18.3.493

Source DB:  PubMed          Journal:  Int J Oncol        ISSN: 1019-6439            Impact factor:   5.650


  16 in total

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Authors:  Lizhi He; Alistair Ingram; Adrian P Rybak; Damu Tang
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Review 3.  PI3K/PTEN signaling in angiogenesis and tumorigenesis.

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Journal:  Adv Cancer Res       Date:  2009       Impact factor: 6.242

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Journal:  Virchows Arch       Date:  2003-04-15       Impact factor: 4.064

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Authors:  Mei Ming; Yu-Ying He
Journal:  J Invest Dermatol       Date:  2009-04-02       Impact factor: 8.551

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Journal:  World J Gastroenterol       Date:  2003-03       Impact factor: 5.742

7.  Methylation of the PTEN promoter defines low-grade gliomas and secondary glioblastoma.

Authors:  John K Wiencke; Shichun Zheng; Nanette Jelluma; Tarik Tihan; Scott Vandenberg; Tanja Tamgüney; Rachel Baumber; Ramon Parsons; Kathleen R Lamborn; Mitchel S Berger; Margaret R Wrensch; Daphne Adele Haas-Kogan; David Stokoe
Journal:  Neuro Oncol       Date:  2007-05-15       Impact factor: 12.300

8.  PRDM4 inhibits cell proliferation and tumorigenesis by inactivating the PI3K/AKT signaling pathway through targeting of PTEN in cervical carcinoma.

Authors:  Wen-Ting Yang; Mei Chen; Rui Xu; Peng-Sheng Zheng
Journal:  Oncogene       Date:  2021-04-12       Impact factor: 9.867

9.  The drug-resistance to gefitinib in PTEN low expression cancer cells is reversed by irradiation in vitro.

Authors:  Hong-Qing Zhuang; Jun Wang; Zhi-Yong Yuan; Lu-Jun Zhao; Ping Wang; Chang-Li Wang
Journal:  J Exp Clin Cancer Res       Date:  2009-09-01

10.  UVB-induced ERK/AKT-dependent PTEN suppression promotes survival of epidermal keratinocytes.

Authors:  M Ming; W Han; J Maddox; K Soltani; C R Shea; D M Freeman; Y-Y He
Journal:  Oncogene       Date:  2009-11-02       Impact factor: 9.867

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