Phosphatidylinositol 3-kinase (PI3K) pathway activation in bladder cancer

被引:128
作者
Knowles, Margaret A. [1 ]
Platt, Fiona M. [1 ]
Ross, Rebecca L. [1 ]
Hurst, Carolyn D. [1 ]
机构
[1] St James Univ Hosp, Leeds Inst Mol Med, Canc Res UK Clin Ctr, Leeds LS9 7TF, W Yorkshire, England
基金
英国医学研究理事会;
关键词
Bladder cancer; PI3K pathway; PTEN; PIK3CA; AKT1; TSC1; TRANSITIONAL-CELL CARCINOMA; TUBEROUS SCLEROSIS COMPLEX; EPIDERMAL-GROWTH-FACTOR; TUMOR-SUPPRESSOR LOCI; INVASIVE UROTHELIAL CARCINOMA; PEUTZ-JEGHERS-SYNDROME; C-ERBB-2; GENE-PRODUCT; ERBB FAMILY RECEPTORS; URINARY-BLADDER; MISSENSE MUTATIONS;
D O I
10.1007/s10555-009-9198-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The phosphatidylinositol 3-kinase (PI3K) pathway is a critical signal transduction pathway that regulates multiple cellular functions. Aberrant activation of this pathway has been identified in a wide range of cancers. Several pathway components including AKT, PI3K and mTOR represent potential therapeutic targets and many small molecule inhibitors are in development or early clinical trials. The complex regulation of the pathway, together with the multiple mechanisms by which it can be activated, make this a highly challenging pathway to target. For successful inhibition, detailed molecular information on individual tumours will be required and it is already clear that different tumour types show distinct combinations of alterations. Recent results have identified alterations in pathway components PIK3CA, PTEN, AKT1 and TSC1 in bladder cancer, some of which are significantly related to tumour phenotype and clinical behaviour. Co-existence of alterations to several PI3K pathway genes in some bladder tumours indicates that these proteins may have functions that are not related solely to the known canonical pathway.
引用
收藏
页码:305 / 316
页数:12
相关论文
共 90 条
[1]   Human bladder tumors with 2-hit mutations of the tumor suppressor gene TSC1 and decreased expression of p27 [J].
Adachi, H ;
Igawa, M ;
Shiina, H ;
Urakami, S ;
Shigeno, K ;
Hino, O .
JOURNAL OF UROLOGY, 2003, 170 (02) :601-604
[2]  
Adley BP, 2006, ARCH PATHOL LAB MED, V130, P1865
[3]  
ASKHAM JM, 2009, ONCOGENE IN PRESS
[4]   Somatic mutation of PTEN in bladder carcinoma [J].
Aveyard, JS ;
Skilleter, A ;
Habuchi, T ;
Knowles, MA .
BRITISH JOURNAL OF CANCER, 1999, 80 (5-6) :904-908
[5]   Frequent FGFR3 mutations in papillary non-invasive bladder (pTa) tumors [J].
Billerey, C ;
Chopin, D ;
Aubriot-Lorton, MH ;
Ricol, D ;
de Medina, SGD ;
Van Rhijn, B ;
Bralet, MP ;
Lefrere-Belda, MA ;
Lahaye, JB ;
Abbou, CC ;
Bonaventure, J ;
Zafrani, ES ;
van der Kwast, T ;
Thiery, JP ;
Radvanyi, F .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (06) :1955-1959
[6]   PKBα/Akt1 acts downstream of DNA-PK in the DNA double-strand break response and promotes survival [J].
Bozulic, Lana ;
Surucu, Banu ;
Hynx, Debby ;
Hemmings, Brian A. .
MOLECULAR CELL, 2008, 30 (02) :203-213
[7]  
CAIRNS P, 1993, ONCOGENE, V8, P1083
[8]   Point mutation and homozygous deletion of PTEN/MMAC1 in primary bladder cancers [J].
Cairns, P ;
Evron, E ;
Okami, K ;
Halachmi, N ;
Esteller, M ;
Herman, JG ;
Bose, S ;
Wang, SI ;
Parsons, R ;
Sidransky, D .
ONCOGENE, 1998, 16 (24) :3215-3218
[9]   The phosphoinositide 3-kinase pathway [J].
Cantley, LC .
SCIENCE, 2002, 296 (5573) :1655-1657
[10]   Frequent loss of heterozygosity on chromosome 10q in muscle-invasive transitional cell carcinomas of the bladder [J].
Cappellen, D ;
deMedina, SGD ;
Chopin, D ;
Thiery, JP ;
Radvanyi, F .
ONCOGENE, 1997, 14 (25) :3059-3066