Combination of cadherin-17 and SATB homeobox 2 serves as potential optimal makers for the differential diagnosis of pulmonary enteric adenocarcinoma and metastatic colorectal adenocarcinoma

被引:37
作者
Bian, Tingting [1 ]
Zhao, Jinli [2 ]
Feng, Jia [1 ]
Zhang, Qing [1 ]
Qian, Li [1 ]
Liu, Jian [3 ]
Jiang, Daishan [4 ]
Liu, Yifei [1 ]
Zhang, Jianguo [1 ]
机构
[1] Nantong Univ, Dept Pathol, Affiliated Hosp, Nantong, Jiangsu, Peoples R China
[2] Nantong Univ, Dept Radiol, Affiliated Hosp, Nantong, Jiangsu, Peoples R China
[3] Nantong Univ, Dept Chemotherapy, Affiliated Hosp, Nantong, Jiangsu, Peoples R China
[4] Nantong Univ, Dept Emergency Med, Affiliated Hosp, Nantong, Jiangsu, Peoples R China
关键词
pulmonary enteric adenocarcinoma; metastatic colorectal adenocarcinoma; cadherin-17; SATB homeobox 2; immunohistochemistry; EXPRESSION; MARKER; CARCINOMA; ORIGIN;
D O I
10.18632/oncotarget.18828
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Pulmonary enteric adenocarcinoma (PEAC), a rare type of non-small cell lung cancer, has similar histological and immunohistochemical morphology to colorectal adenocarcinoma. Cadherin-17 (CDH17) and SATB homeobox 2 (SATB2) immunoexpression have recently been demonstrated in colorectal adenocarcinoma. In this study, we evaluated the value of CDH17 and SATB2 in the diagnosis of pulmonary enteric adenocarcinoma and metastatic colorectal adenocarcinoma. Methods: A total of 13 PEAC cases and 27 metastatic colorectal adenocarcinoma cases were enrolled in our cohort study. We analyzed the expressions of CK7, CK20, CDX-2, villin, cadherin-17 (CDH17), and SATB homeobox 2 (SATB2) using immunohistochemistry. Staining intensity and percentage of positive-staining cells were recorded. Sensitivity and specificity values for immunostains, individually and in combination, were computed and compared. Results: Combining CDH17 and SATB2 resulted in high sensitivity (76.92%) and specificity (100%). In our study, the use of CK7+, napsin A+,TTF-1+, napsin A+ TTF-1+ in combination with CDH17-/SATB2- had a higher area under the curve compared to the combination CDH17-/SATB2-. However, no significant differences were observed between the combination CDH17-/SATB2- and other combinations (P>0.05). Conclusions: In combination, CDH17 and SATB2 serve as potential optimal markers for the differential diagnosis of PEAC and metastatic colorectal adenocarcinoma.
引用
收藏
页码:63442 / 63452
页数:11
相关论文
共 33 条
[1]  
[Anonymous], APPL IMMUNOHISTOCHEM
[2]  
[Anonymous], CASE REP PULMONOL
[3]  
[Anonymous], AM J CLIN PATHOL
[4]   The value of CDX2 and cytokeratins 7 and 20 expression in differentiating colorectal adenocarcinomas from extraintestinal gastrointestinal adenocarcinomas: cytokeratin 7-/20+ phenotype is more specific than CDX2 antibody [J].
Bayrak, Reyhan ;
Haltas, Hacer ;
Yenidunya, Sibel .
DIAGNOSTIC PATHOLOGY, 2012, 7
[5]   Cytokeratin 7 and cytokeratin 20 expression in colorectal adenocarcinomas [J].
Bayrak, Reyhan ;
Yenidunya, Sibel ;
Haltas, Hacer .
PATHOLOGY RESEARCH AND PRACTICE, 2011, 207 (03) :156-160
[6]   Young investigator challenge: Cadherin-17 and SATB2 in cytology specimens: Do these new immunostains help in differentiating metastatic colorectal adenocarcinoma from adenocarcinomas of other origins? [J].
Brandler, Tamar C. ;
Jelloul, Fatima-Zahra ;
Soto, Daniel ;
Das, Kasturi ;
Rosen, Lisa ;
Bhuiya, Tawfiqul A. .
CANCER CYTOPATHOLOGY, 2015, 123 (12) :706-712
[7]   Cytokeratin 7 and cytokeratin 20 expression in epithelial neoplasms: A survey of 435 cases [J].
Chu, PG ;
Wu, E ;
Weiss, LM .
MODERN PATHOLOGY, 2000, 13 (09) :962-972
[8]   Metastatic Carcinoma of Unknown Primary: Diagnostic Approach Using Immunohistochemistry [J].
Conner, James R. ;
Hornick, Jason L. .
ADVANCES IN ANATOMIC PATHOLOGY, 2015, 22 (03) :149-167
[9]   COMPARING THE AREAS UNDER 2 OR MORE CORRELATED RECEIVER OPERATING CHARACTERISTIC CURVES - A NONPARAMETRIC APPROACH [J].
DELONG, ER ;
DELONG, DM ;
CLARKEPEARSON, DI .
BIOMETRICS, 1988, 44 (03) :837-845
[10]   Markers of adenocarcinoma characteristic of the site of origin: Development of a diagnostic algorithm [J].
Dennis, JL ;
Hvidsten, TR ;
Wit, EC ;
Komorowski, J ;
Bell, AK ;
Downie, I ;
Mooney, J ;
Verbeke, C ;
Bellamy, C ;
Keith, WN ;
Olien, KA .
CLINICAL CANCER RESEARCH, 2005, 11 (10) :3766-3772