BRAF V600E mutational status in bile duct adenomas and hamartomas

被引:24
作者
Pujals, Anais [1 ,2 ,3 ]
Bioulac-Sage, Paulette [4 ,5 ]
Castain, Claire [4 ,5 ]
Charpy, Cecile [1 ]
Zafrani, Elie Serge [1 ,2 ]
Calderaro, Julien [1 ,2 ,6 ]
机构
[1] CHU Henri Mondor, AP HP, Dept Pathol, F-94010 Creteil, France
[2] Univ Paris Est Creteil, Fac Med, Creteil, France
[3] Inst Mondor Rech Biomed, INSERM U955, Equipe 9, Creteil, France
[4] CHU Bordeaux, Pellegrin Hosp, Dept Pathol, Bordeaux, France
[5] Univ Bordeaux, INSERM, UMR 1053, Bordeaux, France
[6] Inst Mondor Rech Biomed, Inserm U955, Equipe 18, Cr eteil, France
关键词
bile duct adenoma; bile duct hamartoma; BRAF; cholangiocarcinoma; V600E; VON-MEYENBURG COMPLEXES; INTRAHEPATIC CHOLANGIOCARCINOMA; MONOCLONAL-ANTIBODY; IMMUNOHISTOCHEMISTRY; TRANSFORMATION; CARCINOMA; MELANOMA; CANCER; TUMORS;
D O I
10.1111/his.12674
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: Bile duct adenomas (BDA) and bile duct hamartomas (BDH) are benign bile duct lesions considered neoplastic or secondary to ductal plate malformation, respectively. We have reported previously a high prevalence of BRAF V600E mutations detected by allele-specific polymerase chain reaction assay in BDA, and suggested that BDA may be precursors to a subset of intrahepatic cholangiocarcinomas harbouring V600E mutations. The aim of the present study was to assess the existence of BRAF V600E mutations, using immunohistochemical methods, in additional BDA as well as in BDH. Methods and results: Fifteen BDA and 35 BDH were retrieved from the archives of the pathology departments of two French university hospitals. All cases were reviewed by two pathologists specialized in liver diseases. BRAF V600E mutational status was investigated by immunohistochemistry. Mutated BRAF mutant protein was detected in 53% of the BDA and in none of the cases of BDH. Conclusion: Our findings suggest that BDA and BDH are different processes, and that BDA represent true benign neoplasms. They also support the hypothesis that mutated BDA might precede the development of the subset of intrahepatic cholangiocarcinomas harbouring BRAF V600E mutations.
引用
收藏
页码:562 / 567
页数:6
相关论文
共 29 条
[1]   BILE-DUCT ADENOMA - A STUDY OF 152 CASES [J].
ALLAIRE, GS ;
RABIN, L ;
ISHAK, KG ;
SESTERHENN, IA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1988, 12 (09) :708-715
[2]  
[Anonymous], 2010, WHO CLASSIFICATION T
[3]   The serrated pathway to colorectal carcinoma: current concepts and challenges [J].
Bettington, Mark ;
Walker, Neal ;
Clouston, Andrew ;
Brown, Ian ;
Leggett, Barbara ;
Whitehall, Vicki .
HISTOPATHOLOGY, 2013, 62 (03) :367-386
[4]   The so-called bile duct adenoma is a peribiliary gland hamartoma [J].
Bhathal, PS ;
Hughes, NR ;
Goodman, ZD .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1996, 20 (07) :858-864
[5]   Detection of the BRAF V600E mutation in serous ovarian tumors: a comparative analysis of immunohistochemistry with a mutation-specific monoclonal antibody and allele-specific PCR [J].
Boesmueller, Hans ;
Fischer, Anna ;
Pham, Deborah L. ;
Fehm, Tanja ;
Capper, David ;
von Deimling, Andreas ;
Bonzheim, Irina ;
Staebler, Annette ;
Fend, Falko .
HUMAN PATHOLOGY, 2013, 44 (03) :329-335
[6]  
BURNS CD, 1990, ARCH PATHOL LAB MED, V114, P1287
[7]   Assessment of BRAF V600E mutation status by immunohistochemistry with a mutation-specific monoclonal antibody [J].
Capper, David ;
Preusser, Matthias ;
Habel, Antje ;
Sahm, Felix ;
Ackermann, Ulrike ;
Schindler, Genevieve ;
Pusch, Stefan ;
Mechtersheimer, Gunhild ;
Zentgraf, Hanswalter ;
von Deimling, Andreas .
ACTA NEUROPATHOLOGICA, 2011, 122 (01) :11-19
[8]  
Chan TL, 2003, CANCER RES, V63, P4878
[9]   BRAF mutation in papillary thyroid carcinoma [J].
Cohen, J ;
Xing, MZ ;
Mambo, E ;
Guo, ZM ;
Wu, GG ;
Trink, B ;
Beller, U ;
Westra, WH ;
Ladenson, PW ;
Sidransky, D .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (08) :625-627
[10]   Mutations of the BRAF gene in human cancer [J].
Davies, H ;
Bignell, GR ;
Cox, C ;
Stephens, P ;
Edkins, S ;
Clegg, S ;
Teague, J ;
Woffendin, H ;
Garnett, MJ ;
Bottomley, W ;
Davis, N ;
Dicks, N ;
Ewing, R ;
Floyd, Y ;
Gray, K ;
Hall, S ;
Hawes, R ;
Hughes, J ;
Kosmidou, V ;
Menzies, A ;
Mould, C ;
Parker, A ;
Stevens, C ;
Watt, S ;
Hooper, S ;
Wilson, R ;
Jayatilake, H ;
Gusterson, BA ;
Cooper, C ;
Shipley, J ;
Hargrave, D ;
Pritchard-Jones, K ;
Maitland, N ;
Chenevix-Trench, G ;
Riggins, GJ ;
Bigner, DD ;
Palmieri, G ;
Cossu, A ;
Flanagan, A ;
Nicholson, A ;
Ho, JWC ;
Leung, SY ;
Yuen, ST ;
Weber, BL ;
Siegler, HF ;
Darrow, TL ;
Paterson, H ;
Marais, R ;
Marshall, CJ ;
Wooster, R .
NATURE, 2002, 417 (6892) :949-954