Localization of mesothelin in epithelial ovarian cancer

被引:143
作者
Hassan, R
Kreitman, RJ
Pastan, I
Willingham, MC
机构
[1] NCI, Mol Biol Lab, NIH, Bethesda, MD 20892 USA
[2] Wake Forest Univ, Sch Med, Dept Pathol, Winston Salem, NC 27109 USA
来源
APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY | 2005年 / 13卷 / 03期
关键词
mesothelin; ovarian cancer; immunohistochemistry;
D O I
10.1097/01.pai.00000141545.36485.d6
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Mesothelin is a cell surface glycoprotein that is present on normal mesothelial cells and overexpressed in several cancers. On immunohistochemical examination of a limited number of ovarian tumors, increased mesothelin expression has been previously noted. The authors evaluated mesothelin expression in 48 patients with ovarian cancer who were screened for participation in phase I studies of a recombinant immunotoxin targeting mesothelin. Eligibility criteria for participation in the studies included mesothelin expression by more than 30% of accessible tumor cells. Sections of formalin-fixed paraffin-embedded tumor specimens were evaluated for mesothelin expression by immunohistochemistry using the anti-mesothelin monoclonal antibody K1. Between September 2000 and January 2003, 48 ovarian tumors were analyzed for mesothelin positivity. Mesothelin positivity was noted in 34 of the 48 cases evaluated (71%). These results show that mesothelin is expressed in most epithelial ovarian cancers and that mesothelin expression in ovarian cancers can be evaluated in archival material. Patients whose tumors express mesothelin could be eligible for participation in clinical trials of novel agents targeting mesothelin.
引用
收藏
页码:243 / 247
页数:5
相关论文
共 18 条
[1]  
Argani P, 2001, CLIN CANCER RES, V7, P3862
[2]   Mesothelin is not required for normal mouse development or reproduction [J].
Bera, TK ;
Pastan, I .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (08) :2902-2906
[3]   ISOLATION AND CHARACTERIZATION OF A MONOCLONAL-ANTIBODY, K1, REACTIVE WITH OVARIAN CANCERS AND NORMAL MESOTHELIUM [J].
CHANG, K ;
PASTAN, I ;
WILLINGHAM, MC .
INTERNATIONAL JOURNAL OF CANCER, 1992, 50 (03) :373-381
[4]   MONOCLONAL-ANTIBODY K1 REACTS WITH EPITHELIAL MESOTHELIOMA BUT NOT WITH LUNG ADENOCARCINOMA [J].
CHANG, K ;
PAI, LH ;
PASS, H ;
POGREBNIAK, HW ;
TSAO, MS ;
PASTAN, I ;
WILLINGHAM, MC .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1992, 16 (03) :259-268
[5]   Molecular cloning of mesothelin, a differentiation antigen present on mesothelium, mesotheliomas, and ovarian cancers [J].
Chang, K ;
Pastan, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :136-140
[6]   FREQUENT EXPRESSION OF THE TUMOR-ANTIGEN CAK1 IN SQUAMOUS-CELL CARCINOMAS [J].
CHANG, K ;
PASTAN, I ;
WILLINGHAM, MC .
INTERNATIONAL JOURNAL OF CANCER, 1992, 51 (04) :548-554
[7]   Improving antibody affinity by mimicking somatic hypermutation in vitro [J].
Chowdhury, PS ;
Pastan, I .
NATURE BIOTECHNOLOGY, 1999, 17 (06) :568-572
[8]   Isolation of a high-affinity stable single-chain Fv specific for mesothelin from DNA-immunized mice by phage display and construction of a recombinant immunotoxin with anti-tumor activity [J].
Chowdhury, PS ;
Viner, JL ;
Beers, R ;
Pastan, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (02) :669-674
[9]   Large-scale molecular and tissue microarray analysis of mesothelin expression in common human carcinomas [J].
Frierson, HF ;
Moskaluk, CA ;
Powell, SM ;
Zhang, H ;
Cerilli, LA ;
Stoler, MH ;
Cathro, H ;
Hampton, GM .
HUMAN PATHOLOGY, 2003, 34 (06) :605-609
[10]  
Hassan R, 2002, CLIN CANCER RES, V8, P3520