Large-scale analysis ofBAP1expression reveals novel associations with clinical and molecular features of malignant pleural mesothelioma

被引:29
作者
De Rienzo, Assunta [1 ,2 ,3 ,4 ]
Chirieac, Lucian R. [4 ,5 ]
Hung, Yin P. [4 ,6 ]
Severson, David T. [1 ,2 ,3 ,4 ]
Freyaldenhoven, Samuel [1 ,2 ,3 ,4 ,9 ]
Gustafson, Corinne E. [1 ,2 ,3 ,4 ]
Dao, Nhien T. [1 ,2 ,3 ,4 ,10 ]
Meyerovitz, Claire, V [1 ,2 ,3 ,4 ]
Oster, Michela E. [1 ,2 ,3 ,4 ]
Jensen, Roderick, V [7 ]
Yeap, Beow Y. [4 ,8 ]
Bueno, Raphael [1 ,2 ,3 ,4 ]
Richards, William G. [1 ,2 ,3 ,4 ]
机构
[1] Brigham & Womens Hosp, Thorac Surg Oncol Lab, 75 Francis St, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Int Mesothelioma Program Www Impmeso Org, Div Thorac Surg, 75 Francis St, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Lung Ctr, 75 Francis St, Boston, MA 02115 USA
[4] Harvard Med Sch, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
[6] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[7] Virginia Tech, Dept Biol Sci, Blacksburg, VA USA
[8] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[9] USF Hlth South, Dept Surg, 2 Tampa Gen Circle, Tampa, FL 33606 USA
[10] Takeda, 300 Massachusetts Ave, Cambridge, MA 02139 USA
关键词
mesothelioma; BAP1; immunohistochemistry; tumor suppressor gene; intra-tumor heterogeneity; epithelial-to-mesenchymal transition; gene expression; prognostic biomarker; BRCA1-ASSOCIATED PROTEIN-1; BAP1; IMMUNOHISTOCHEMISTRY; TUMOR-SUPPRESSOR; P16; FISH; EXPRESSION; DIAGNOSIS; GENE; MUTATIONS; ACCURACY; CANCER;
D O I
10.1002/path.5551
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BRCA1-associated protein-1(BAP1) expression is commonly lost in several tumors including malignant pleural mesothelioma (MPM). Presence or absence of immunohistochemical BAP1 nuclear staining in tumor cells is currently used for differential diagnosis of MPM. In this study, a large cohort of 596 MPM tumors with available clinical data was analyzed to examine associations of BAP1 staining pattern with clinical and molecular features that may reflect the impact ofBAP1mutation on MPM biology. Cases were classified according to the BAP1 staining pattern of tumor cells. Exome and RNA-sequencing data were available for subsets of cases. Levels of mRNA encoding claudin 15 (CLDN15) and vimentin (VIM) were determined using RT-qPCR on 483 cases to estimate the relative proportions of epithelial-like and mesenchymal-like components in each tumor. Four BAP1 staining patterns were observed: single-pattern nuclear staining (36%), single-pattern cytoplasmic staining (25%), single-pattern absent staining (12%), and combinations of these staining patterns (27%). This study confirmed prior reports that nuclear BAP1 is more frequently associated with wild-typeBAP1and sarcomatoid histology. However, no associations between BAP1 staining pattern(s) and mutations in specific protein domains and/or mutation type were observed. BAP1 staining patterns were significantly associated (p < 0.001) withBAP1gene expression, MPM histologic subtypes, molecular clusters, and markers of epithelial-to-mesenchymal transition. Frequent observation of combinations of BAP1 staining patterns in MPM tumors indicated intra-tumoral heterogeneity ofBAP1status. Cytoplasmic BAP1 staining was identified as a putative indicator of favorable prognosis in non-epithelioid MPM. In conclusion, novel significant associations among different BAP1 staining patterns and subgroups of MPM tumors were observed, suggesting that the role ofBAP1in tumor progression may be more complex than its presumed tumor suppressor function. Cytoplasmic staining was identified as a putative indicator of favorable prognosis in non-epithelioid MPM, potentially addressing a critical need in clinical decision-making in this disease. (c) 2020 The Authors.The Journal of Pathologypublished by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland.
引用
收藏
页码:68 / 79
页数:12
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