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VSTM2A Overexpression Is a Sensitive and Specific Biomarker for Mucinous Tubular and Spindle Cell Carcinoma (MTSCC) of the Kidney
Author(s) -
Lisha Wang,
Yuping Zhang,
Ying-Bei Chen,
Stephanie L. Skala,
Hikmat AlAhmadie,
Xiaoming Wang,
Xuhong Cao,
Brendan Veeneman,
Jin Chen,
Marcin Cieślik,
Yuanyuan Qiao,
Fengyun Su,
Pankaj Vats,
Javed Siddiqui,
Hong Xiao,
Evita Sadimin,
Jonathan I. Epstein,
Ming Zhou,
Ankur R. Sangoi,
Kiril Trpkov,
Adeboye O. Osunkoya,
Giovanna Giannico,
Jesse K. McKenney,
Pedram Argani,
Satish K. Tickoo,
Victor E. Reuter,
Arul M. Chinnaiyan,
Saravana M. Dhanasekaran,
Rohit Mehra
Publication year - 2018
Publication title -
the american journal of surgical pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.625
H-Index - 210
eISSN - 1532-0979
pISSN - 0147-5185
DOI - 10.1097/pas.0000000000001150
Subject(s) - biomarker , biology , cancer , pathology , renal cell carcinoma , in situ hybridization , cancer research , medicine , gene expression , gene , genetics
Our recent study revealed recurrent chromosomal losses and somatic mutations of genes in the Hippo pathway in mucinous tubular and spindle cell carcinoma (MTSCC). Here, we performed an integrative analysis of 907 renal cell carcinoma (RCC) samples (combined from The Cancer Genome Atlas and in-house studies) and the Knepper data set of microdissected rat nephrons. We identified VSTM2A and IRX5 as novel cancer-specific and lineage-specific biomarkers in MTSCC. We then assessed their expression by RNA in situ hybridization (ISH) in 113 tumors, including 33 MTSCC, 40 type 1 papillary RCC, 8 type 2 papillary RCC, 2 unclassified RCC, 15 clear cell RCC, and 15 chromophobe RCC. Sensitivity and specificity were calculated as the area under the receiver operating characteristics curve (AUC). All MTSCC tumors demonstrated moderate to high expression of VSTM2A (mean ISH score=255). VSTM2A gene expression assessed by RNA sequencing strongly correlated with VSTM2A ISH score (r(2)=0.81, P=0.00016). The majority of non-MTSCC tumors demonstrated negative or low expression of VSTM2A. IRX5, nominated as a lineage-specific biomarker, showed moderate to high expression in MTSCC tumors (mean ISH score=140). IRX5 gene expression assessed by RNA sequencing strongly correlated with IRX5 ISH score (r(2)=0.69, P=0.00291). VSTM2A (AUC: 99.2%) demonstrated better diagnostic efficacy than IRX5 (AUC: 87.5%), and may thus serve as a potential diagnostic marker to distinguish tumors with overlapping histology. Furthermore, our results suggest MTSCC displays an overlapping phenotypic expression pattern with the loop of Henle region of normal nephrons.

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