Effects of PTEN gene alteration in patients with gallbladder cancer

被引:15
作者
Ali, Asgar [1 ]
Mishra, Pramod Kumar [2 ]
Sharma, Sadhana [1 ]
Arora, Asit [2 ]
Saluja, Sundeep Singh [2 ]
机构
[1] All India Inst Med Sci, Dept Biochem, Patna, Bihar, India
[2] GB Pant Hosp, Dept Gastrointestinal Surg, New Delhi, India
关键词
PTEN; gallbladder cancer; mutation; immunohistochemistry; hypermethylation and single-strand conformation polymorphism; PROMOTER METHYLATION; TUMOR-SUPPRESSOR; PTEN/MMAC1; EXPRESSION; MUTATION; PROTEIN; PROGRESSION; CARCINOMA; PATHWAY; BREAST;
D O I
10.1016/j.cancergen.2015.09.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gallbladder cancer (GBC) is an aggressive malignancy usually diagnosed in an advanced stage. We investigated the effects of alterations of the phosphatase and tensin homologue (PTEN) gene on the occurrence and development of GBC, which has not been previously reported. A total 141 cases of GBC were analyzed for mutation, expression, and methylation across the nine exons of the PTEN gene. DNA sequencing methods were applied for mutation detection, whereas protein expression and methylation status were evaluated by immunohistochemical and methylationspecific PCR analysis, respectively. Novel PTEN mutations were observed in 6.3% of cases (9/141), and they included two silent mutations. In mutant cases, according to changes in codons, the respective amino acid sequences were also changed, which caused of proteins. A high percentage (72%) of loss of protein expression was observed more often in cases than in control samples. Interestingly, all nine cases with mutations showed loss of PTEN expression, whereas four of these nine cases showed positive promoter methylation. Hypermethylation was significantly more common in older patients than in younger ones (P < 0.02). These findings suggest that PTEN mutations and inactivation may play an important role in the development and progression of gallbladder carcinoma.
引用
收藏
页码:587 / 594
页数:8
相关论文
共 26 条
[1]   Mutational and Expressional Analyses of PTEN Gene in Colorectal Cancer From Northern India [J].
Ali, Asgar ;
Saluja, Sundeep S. ;
Hajela, Krishnan ;
Mishra, Pramod K. ;
Rizvi, Moshahid A. .
MOLECULAR CARCINOGENESIS, 2014, 53 :E45-E52
[2]   PTEN/MMAC1/TEP1 in signal transduction and tumorigenesis [J].
Besson, A ;
Robbins, SM ;
Yong, VW .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 263 (03) :605-611
[3]   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
[4]   PTEN and the PI3-Kinase Pathway in Cancer [J].
Chalhoub, Nader ;
Baker, Suzanne J. .
ANNUAL REVIEW OF PATHOLOGY-MECHANISMS OF DISEASE, 2009, 4 :127-150
[5]   Epigenetic and genetic alternation of PTEN in cervical neoplasm [J].
Cheung, TH ;
Lo, KWK ;
Yim, SF ;
Chan, LKY ;
Heung, MS ;
Chan, CS ;
Cheung, AYK ;
Chung, TKH ;
Wong, YF .
GYNECOLOGIC ONCOLOGY, 2004, 93 (03) :621-627
[6]   Expression of MMP-2,TIMP-2 protein and the ratio of MMP-2/TIMP-2 in gallbladder carcinoma and their significance [J].
Fan, YZ ;
Zhang, JT ;
Yang, HC ;
Yang, YQ .
WORLD JOURNAL OF GASTROENTEROLOGY, 2002, 8 (06) :1138-1143
[7]   p16INK4a is a prognostic marker in resected ductal pancreatic cancer -: An analysis of p16INK4a, p53, MDM2, an Rb [J].
Gerdes, B ;
Ramaswamy, A ;
Ziegler, A ;
Lang, SA ;
Kersting, M ;
Baumann, R ;
Wild, A ;
Moll, R ;
Rothmund, M ;
Bartsch, DK .
ANNALS OF SURGERY, 2002, 235 (01) :51-59
[8]   PCR-SSCP-DNA sequencing method in detecting PTEN gene mutation and its significance in human gastric cancer [J].
Guo, Chuan-Yong ;
Xu, Xuan-Fu ;
Wu, Lian-Ye ;
Liu, Shu-Fang .
WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (24) :3804-3811
[9]   Promoter methylation and silencing of PTEN in gastric carcinoma [J].
Kang, YH ;
Lee, HS ;
Kim, WH .
LABORATORY INVESTIGATION, 2002, 82 (03) :285-291
[10]   Understanding PTEN regulation:: PIP2, polarity and protein stability [J].
Leslie, N. R. ;
Batty, I. H. ;
Maccario, H. ;
Davidson, L. ;
Downes, C. P. .
ONCOGENE, 2008, 27 (41) :5464-5476