Loss of PTEN expression followed by Akt phosphorylation is a poor prognostic factor for patients with endometrial cancer

被引:123
作者
Terakawa, N [1 ]
Kanamori, Y [1 ]
Yoshida, S [1 ]
机构
[1] Tottori Univ, Sch Med, Dept Obstet & Gynecol, Yonago, Tottori 6838504, Japan
关键词
D O I
10.1677/erc.0.0100203
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To clarify whether and how PTEN and the phosphatidylinositol 3-kinase/Akt pathway relates to endometrial cancer we examined the expression of these pathway-related proteins in patients with endometrial cancer. Of 103 endometrial cancers, 37 (36%) showed negative immunohistochemical staining for PTEN. Western blotting revealed that the level of phosphorylated Akt expression in PTEN-negative cases was significantly higher compared with that in positive cases. We found a significant inverse correlation between PTEN and phosphorylated Akt. The present study indicates the phosphorylation of Akt accompanied by the loss of PTEN in clinical specimens of endometrial cancers. In order to investigate the relationship between PTEN expression and prognosis in endometrial cancer, 98 patients with advanced endometrial cancer were newly enrolled. The survival rate for PTEN-positive patients was significantly higher than that for PTEN-negative or -heterogeneous staining patients. Of the 98 patients, 25 underwent radiation therapy, 62 received chemotherapy after surgery, and the remaining 11 did not have any postoperative treatment. When patients underwent chemotherapy, the survival rate for PTEN-positive cases was clearly higher than that for PTEN-negative or -heterogeneous cases (62.4 vs 11.8%). Subsequent multivariate analysis revealed that PTEN staining was an independent prognostic factor for patients undergoing chemotherapy. The current study demonstrates that PTEN-positive staining is a significant prognostic indicator of favorable survival for patients with advanced endometrial cancer who undergo postoperative chemotherapy.
引用
收藏
页码:203 / 208
页数:6
相关论文
共 20 条
[1]  
BERCHUCK A, 1995, CANCER, V76, P2034, DOI 10.1002/1097-0142(19951115)76:10+<2034::AID-CNCR2820761321>3.0.CO
[2]  
2-U
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   The multiple roles of PTEN in tumor suppression [J].
Di Cristofano, A ;
Pandolfi, PP .
CELL, 2000, 100 (04) :387-390
[5]   Crystal structure of the PTEN tumor suppressor: Implications for its phosphoinositide phosphatase activity and membrane association [J].
Lee, JO ;
Yang, HJ ;
Georgescu, MM ;
Di Cristofano, A ;
Maehama, T ;
Shi, YG ;
Dixon, JE ;
Pandolfi, P ;
Pavletich, NP .
CELL, 1999, 99 (03) :323-334
[6]  
Levine RL, 1998, CANCER RES, V58, P3254
[7]   Genetic deletion of the Pten tumor suppressor gene promotes cell motility by activation of Rac1 and Cdc42 GTPases [J].
Liliental, J ;
Moon, SY ;
Lesche, R ;
Mamillapalli, R ;
Li, DM ;
Zheng, Y ;
Sun, H ;
Wu, H .
CURRENT BIOLOGY, 2000, 10 (07) :401-404
[8]   The tumor suppressor, PTEN/MMAC1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate [J].
Maehama, T ;
Dixon, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (22) :13375-13378
[9]   Molecular pathology of endometrial hyperplasia and carcinoma [J].
Matias-Guiu, X ;
Catasus, L ;
Bussaglia, E ;
Lagarda, H ;
Garcia, A ;
Pons, C ;
Muñoz, J ;
Argüelles, R ;
Machin, P ;
Prat, J .
HUMAN PATHOLOGY, 2001, 32 (06) :569-577
[10]  
Maxwell GL, 1998, CANCER RES, V58, P2500