Positive nuclear BAP1 immunostaining helps differentiate non-small cell lung carcinomas from malignant mesothelioma

被引:46
作者
Carbone, Michele [1 ]
Shimizu, David [2 ]
Napolitano, Andrea [1 ]
Tanji, Mika [1 ]
Pass, Harvey I. [3 ]
Yang, Haining [1 ]
Pastorino, Sandra [1 ]
机构
[1] Univ Hawaii, Ctr Canc, Thorac Oncol Program, Honolulu, HI 96822 USA
[2] Queen Med Ctr, Dept Pathol, Honolulu, HI USA
[3] NYU, NYU Langone Med Ctr, Dept Cardiothorac Surg, New York, NY 10003 USA
关键词
mesothelioma; lung cancer; BAP1; differential diagnosis; immunohistochemistry; EXPRESSION; MUTATIONS; DIAGNOSIS; EXPOSURE; ASBESTOS; GENE;
D O I
10.18632/oncotarget.10653
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The differential diagnosis between pleural malignant mesothelioma (MM) and lung cancer is often challenging. Immunohistochemical (IHC) stains used to distinguish these malignancies include markers that are most often positive in MM and less frequently positive in carcinomas, and vice versa. However, in about 10-20% of the cases, the IHC results can be confusing and inconclusive, and novel markers are sought to increase the diagnostic accuracy. We stained 45 non-small cell lung cancer samples (32 adenocarcinomas and 13 squamous cell carcinomas) with a monoclonal antibody for BRCA1-associated protein 1 (BAP1) and also with an IHC panel we routinely use to help differentiate MM from carcinomas, which include, calretinin, Wilms Tumor 1, cytokeratin 5, podoplanin D240, pankeratin CAM5.2, thyroid transcription factor 1, Napsin-A, and p63. Nuclear BAP1 expression was also analyzed in 35 MM biopsies. All 45 non-small cell lung cancer biopsies stained positive for nuclear BAP1, whereas 22/35 (63%) MM biopsies lacked nuclear BAP1 staining, consistent with previous data. Lack of BAP1 nuclear staining was associated with MM (two-tailed Fisher's Exact Test, P = 5.4 x 10(-11)). Focal BAP1 staining was observed in a subset of samples, suggesting polyclonality. Diagnostic accuracy of other classical IHC markers was in agreement with previous studies. Our study indicated that absence of nuclear BAP1 stain helps differentiate MM from lung carcinomas. We suggest that BAP1 staining should be added to the IHC panel that is currently used to distinguish these malignancies.
引用
收藏
页码:59314 / 59321
页数:8
相关论文
共 42 条
[1]   Loss of expression of BAP1 is very rare in non-small cell lung carcinoma [J].
Andrici, Juliana ;
Parkhill, Thomas R. ;
Jung, Jason ;
Wardell, Kathryn L. ;
Verdonk, Brandon ;
Singh, Arjun ;
Sioson, Loretta ;
Clarkson, Adele ;
Watson, Nicole ;
Sheen, Amy ;
Farzin, Mahtab ;
Toon, Christopher W. ;
Gill, Anthony J. .
PATHOLOGY, 2016, 48 (04) :336-340
[2]   Loss of BAP1 expression is very rare in peritoneal and gynecologic serous adenocarcinomas and can be useful in the differential diagnosis with abdominal mesothelioma [J].
Andrici, Juliana ;
Jung, Jason ;
Sheen, Amy ;
D'Urso, Lisa ;
Sioson, Loretta ;
Pickett, Justine ;
Parkhill, Thomas R. ;
Verdonk, Brandon ;
Wardell, Kathryn L. ;
Singh, Arjun ;
Clarkson, Adele ;
Watson, Nicole ;
Toon, Christopher W. ;
Gill, Anthony J. .
HUMAN PATHOLOGY, 2016, 51 :9-15
[3]   Loss of expression of BAP1 is a useful adjunct, which strongly supports the diagnosis of mesothelioma in effusion cytology [J].
Andrici, Juliana ;
Sheen, Amy ;
Sioson, Loretta ;
Wardell, Kathryn ;
Clarkson, Adele ;
Watson, Nicole ;
Ahadi, Mahsa S. ;
Farzin, Mahtab ;
Toon, Christopher W. ;
Gill, Anthony J. .
MODERN PATHOLOGY, 2015, 28 (10) :1360-1368
[4]   BAP1 Protein is a Progression Factor in Malignant Pleural Mesothelioma [J].
Arzt, Lisa ;
Quehenberger, Franz ;
Halbwedl, Iris ;
Mairinger, Thomas ;
Popper, Helmut H. .
PATHOLOGY & ONCOLOGY RESEARCH, 2014, 20 (01) :145-151
[5]   The Presence of Asbestos in the Natural Environment is Likely Related to Mesothelioma in Young Individuals and Women from Southern Nevada [J].
Baumann, Francine ;
Buck, Brenda J. ;
Metcalf, Rodney V. ;
McLaurin, Brett T. ;
Merkler, Douglas J. ;
Carbone, Michele .
JOURNAL OF THORACIC ONCOLOGY, 2015, 10 (05) :731-737
[6]   The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma [J].
Bott, Matthew ;
Brevet, Marie ;
Taylor, Barry S. ;
Shimizu, Shigeki ;
Ito, Tatsuo ;
Wang, Lu ;
Creaney, Jenette ;
Lake, Richard A. ;
Zakowski, Maureen F. ;
Reva, Boris ;
Sander, Chris ;
Delsite, Robert ;
Powell, Simon ;
Zhou, Qin ;
Shen, Ronglai ;
Olshen, Adam ;
Rusch, Valerie ;
Ladanyi, Marc .
NATURE GENETICS, 2011, 43 (07) :668-U81
[7]   Comprehensive genomic analysis of malignant pleural mesothelioma identifies recurrent mutations, gene fusions and splicing alterations [J].
Bueno, Raphael ;
Stawiski, Eric W. ;
Goldstein, Leonard D. ;
Durinck, Steffen ;
De Rienzo, Assunta ;
Modrusan, Zora ;
Gnad, Florian ;
Nguyen, Thong T. ;
Jaiswal, Bijay S. ;
Chirieac, Lucian R. ;
Sciaranghella, Daniele ;
Dao, Nhien ;
Gustafson, Corinne E. ;
Munir, Kiara J. ;
Hackney, Jason A. ;
Chaudhuri, Amitabha ;
Gupta, Ravi ;
Guillory, Joseph ;
Toy, Karen ;
Ha, Connie ;
Chen, Ying-Jiun ;
Stinson, Jeremy ;
Chaudhuri, Subhra ;
Zhang, Na ;
Wu, Thomas D. ;
Sugarbaker, David J. ;
de Sauvage, Frederic J. ;
Richards, William G. ;
Seshagiri, Somasekar .
NATURE GENETICS, 2016, 48 (04) :407-+
[8]  
Carbone M, 2000, J CELL BIOCHEM, V76, P189, DOI 10.1002/(SICI)1097-4644(20000201)76:2<189::AID-JCB3>3.0.CO
[9]  
2-J
[10]   A mesothelioma epidemic in Cappadocia: scientific developments and unexpected social outcomes [J].
Carbone, Michele ;
Emri, Salih ;
Dogan, A. Umran ;
Steele, Ian ;
Tuncer, Murat ;
Pass, Harvey I. ;
Baris, Y. Izzettin .
NATURE REVIEWS CANCER, 2007, 7 (02) :147-154