Up-regulation of PTEN at the transcriptional level is an adverse prognostic factor in female lung adenocarcinomas

被引:19
作者
Inamura, Kentaro
Togashi, Yuki
Nomura, Kimie
Ninomiya, Hironori
Hiramatsu, Miyako
Okui, Michiyo
Satoh, Yukitoshi
Okumura, Sakae
Nakagawa, Ken
Tsuchiya, Eiju
Ishikawa, Yuichi
机构
[1] Japanese Fdn Canc Res, Dept Pathol, Koto Ku, Tokyo 1358550, Japan
[2] Japanese Fdn Canc Res, Dept Chest Surg, Koto Ku, Tokyo 1358550, Japan
[3] Kanagawa Canc Ctr, Res Inst, Asahi Ku, Yokohama, Kanagawa 2410815, Japan
基金
日本学术振兴会;
关键词
lung adenocarcinoma; PTEN; real time RT-PCR; prognostic factor;
D O I
10.1016/j.lungcan.2007.03.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In lung adenocarcinomas, genetic alterations of PTEN are relatively rare and Little has been reported concerning the relationship between PTEN transcriptional level and clinicopathologic features or genetic changes. This study was conducted to gain insight into clinicopathologic correlations. The transcriptional levels of PTEN were examined using real time RT-PCR and analyzed for correlations with clinicopathologic features and the mutation status of EGFR and KRAS. After confirming significant correlation for PTEN levels between macrodissected and microdissected materials (p < 0.01), macrodissected samples from 115 lung adenocarcinomas were examined. There were no significant difference between the PTEN levels, divided into three ranges, and the mutation status of EGFR or KRAS. Noteworthy clinicopathologic correlations between PTEN transcriptional up/down-regulation and young age (p=0.0081, 61.7 +/- 8.7 years versus 66.1 +/- 8.1 years), smoking (p = 0.032) and less differentiated adenocarcinomas (p = 0.013) were identified. Whereas male patients demonstrated no prognostic association with PTEN levels, female cases with up-regulated PTEN expression had significantly worse survival compared with those with normal PTEN levels (p = 0.0027). This study revealed distinct clinicopathologic correlations with PTEN transcriptional up/down-regulation. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:201 / 206
页数:6
相关论文
共 26 条
[1]  
[Anonymous], GEN RUL CLIN PATH RE
[2]   RRM1 and PTEN as prognostic parameters for overall and disease-free survival in patients with non-small-cell lung cancer [J].
Bepler, G ;
Sharma, S ;
Cantor, A ;
Gautam, A ;
Haura, E ;
Simon, G ;
Sharma, A ;
Sommers, E ;
Robinson, L .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (10) :1878-1885
[3]  
Cairns P, 1997, CANCER RES, V57, P4997
[4]   PTEN mutations in gliomas and glioneuronal tumors [J].
Duerr, EM ;
Rollbrocker, B ;
Hayashi, Y ;
Peters, N ;
Meyer-Puttlitz, B ;
Louis, DN ;
Schramm, J ;
Wiestler, OD ;
Parsons, R ;
Eng, C ;
von Deimling, A .
ONCOGENE, 1998, 16 (17) :2259-2264
[5]   Mutation analysis of the PTEN/MMAC1 gene in lung cancer [J].
Forgacs, E ;
Biesterveld, EJ ;
Sekido, Y ;
Fong, K ;
Muneer, S ;
Wistuba, II ;
Milchgrub, S ;
Brezinschek, R ;
Virmani, A ;
Gazdar, AF ;
Minna, JD .
ONCOGENE, 1998, 17 (12) :1557-1565
[6]   A metastatic signature in entire lung adenocarcinomas irrespective of morphological heterogeneity [J].
Inamura, Kentaro ;
Shimoji, Takashi ;
Ninomiya, Hironori ;
Hiramatsu, Miyako ;
Okui, Michiyo ;
Satoh, Yukitoshi ;
Okumura, Sakae ;
Nakagawa, Ken ;
Noda, Tetsuo ;
Fukayama, Masashi ;
Ishikawa, Yuichi .
HUMAN PATHOLOGY, 2007, 38 (05) :702-709
[7]   Loss of heterozygosity and the smoking index increase with decrease in differentiation of lung adenocarcinomas: etiologic implications [J].
Ishikawa, Y ;
Furuta, R ;
Miyoshi, T ;
Satoh, Y ;
Okumura, S ;
Nakagawa, K ;
Tsuchiya, E .
CANCER LETTERS, 2002, 187 (1-2) :47-51
[8]  
Kohno T, 1998, GENE CHROMOSOME CANC, V22, P152, DOI 10.1002/(SICI)1098-2264(199806)22:2<152::AID-GCC10>3.0.CO
[9]  
2-S
[10]  
Kondo K, 2001, INT J CANCER, V91, P219, DOI 10.1002/1097-0215(200002)9999:9999<::AID-IJC1034>3.0.CO