Mutational profiling reveals PIK3CA mutations in gallbladder carcinoma

被引:74
作者
Deshpande, Vikram [1 ]
Nduaguba, Afamefuna [3 ]
Zimmerman, Stephanie M. [1 ]
Kehoe, Sarah M. [2 ]
MacConaill, Laura E. [2 ]
Lauwers, Gregory Y. [1 ]
Ferrone, Cristina [1 ]
Bardeesy, Nabeel [1 ]
Zhu, Andrew X. [1 ]
Hezel, Aram F. [3 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Ctr Canc Genome Discovery, Boston, MA 02115 USA
[3] Univ Rochester, Sch Med, James P Wilmot Canc Ctr, Rochester, NY 14642 USA
来源
BMC CANCER | 2011年 / 11卷
关键词
BILIARY-TRACT CANCERS; GROWTH-FACTOR-RECEPTOR; INTRAHEPATIC CHOLANGIOCELLULAR CARCINOMA; TUMOR-SUPPRESSOR GENE; K-RAS; BETA-CATENIN; MICROSATELLITE INSTABILITY; P53; OVEREXPRESSION; SOMATIC MUTATIONS; BILE-DUCT;
D O I
10.1186/1471-2407-11-60
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The genetics of advanced biliary tract cancers (BTC), which encompass intra- and extra-hepatic cholangiocarcinomas as well as gallbladder carcinomas, are heterogeneous and remain to be fully defined. Methods: To better characterize mutations in established known oncogenes and tumor suppressor genes we tested a mass spectrometric based platform to interrogate common cancer associated mutations across a panel of 77 formalin fixed paraffin embedded archived BTC cases. Results: Mutations among three genes, KRAS, NRAS and PIK3CA were confirmed in this cohort. Activating mutations in PIK3CA were identified exclusively in GBC (4/32, 12.5%). KRAS mutations were identified in 3 (13%) intra- hepatic cholangiocarcinomas and 1 (33%) perihillar cholangiocarcinoma but were not identified in gallbladder carcinomas and extra-hepatic cholangiocarcinoma. Conclusions: The presence of activating mutations in PIK3CA specifically in GBC has clinical implications in both the diagnosis of this cancer type, as well as the potential utility of targeted therapies such as PI3 kinase inhibitors.
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页数:7
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