Expression of S100a, vimentin, NSE, and Melan A/MART-1 in seven canine melanoma cell lines and twenty-nine retrospective cases of canine melanoma

被引:55
作者
Koenig, A
Wojcieszyn, J
Weeks, BR
Modiano, JF
机构
[1] AMC Canc Res Ctr, Ctr Canc Causat & Prevent, Denver, CO 80214 USA
[2] Texas A&M Univ, Coll Vet Med, Dept Small Anim Med & Surg, College Stn, TX 77843 USA
[3] Texas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USA
[4] IHC Serv, Smithville, TX USA
[5] Univ Colorado, Ctr Canc, Denver, CO 80262 USA
关键词
dogs; immunohistochemistry; lineage markers; melanoma;
D O I
10.1354/vp.38-4-427
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We evaluated the expression of vimentin, S100a, and Melan A/MART-1 (melanoma antigen recognized by T cells 1) in seven cell lines established independently from dogs with canine melanoma. We also compared routine immunostaining of 29 clinical specimens from melanoma cases using vimentin, S100a, and neuron-specific enolase (NSE) with staining for Melan A/MART-1 as part of a diagnostic panel. All the cell lines were positive for expression of vimentin and S-100a. MelanA/MART-1 expression was seen consistently in only two of the seven cell Lines. Staining for Melan A/MART-1 was most intense near areas of heavy melanin pigmentation. All except one of the clinical specimens were positive for vimentin. S100a was expressed in the majority of both pigmented (15/20, 75%) and amelanotic (8/9, 88.8%) tumors. Seventeen of 29 (58.6%) tumors were positive for NSE. Melan A/MART-1 was expressed in 18/29 (62%) tumors, including 90% of pigmented tumors, but in no amelanotic tumors. Intensity of Melan A/MART-1 staining correlated positively with biologic behavior, with seven malignant tumors showing negative to weak staining and 10 benign tumors showing moderate to strong staining. Three malignant tumors showed moderate to intense staining for Melan A/MART-1. Our results suggest that expression of Melan A/MART-1 may be unstable in cultured cell lines. Assessment of both S100a and Melan A/MART-1 expression is useful to confirm a diagnosis of canine melanoma, and Melan A/MART-1 may be especially informative regarding the biologic behavior of these tumors.
引用
收藏
页码:427 / 435
页数:9
相关论文
共 42 条
[1]   S-100 PROTEIN NEGATIVE MALIGNANT-MELANOMA - FACT OR FICTION - A LIGHT-MICROSCOPIC AND IMMUNOHISTOCHEMICAL STUDY [J].
ARGENYI, ZB ;
CAIN, C ;
BROMLEY, C ;
VANNGUYEN, A ;
ABRAHAM, AA ;
KERSCHMANN, R ;
LEBOIT, PE .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1994, 16 (03) :233-240
[2]  
ARONSOHN MG, 1990, J AM ANIM HOSP ASSOC, V26, P605
[3]   EPITHELIAL MARKERS IN MALIGNANT-MELANOMA - A STUDY OF PRIMARY LESIONS AND THEIR METASTASES [J].
BENIZHAK, O ;
STARK, P ;
LEVY, R ;
BERGMAN, R ;
LICHTIG, C .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1994, 16 (03) :241-246
[4]   A comparative immunohistochemical study of MART-1 expression in Spitz nevi, ordinary melanocytic nevi, and malignant melanomas [J].
Bergman, R ;
Azzam, H ;
Sprecher, E ;
Manov, L ;
Munichor, M ;
Friedman-Birnbaum, R ;
Ben-Itzhak, O .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 42 (03) :496-500
[5]  
Blessing K, 1998, HISTOPATHOLOGY, V32, P139
[6]   Melan-A, a new melanocytic differentiation marker [J].
Busam, KJ ;
Jungbluth, AA .
ADVANCES IN ANATOMIC PATHOLOGY, 1999, 6 (01) :12-18
[7]   Expression of Melan-A (MART1) in benign melanocytic nevi and primary cutaneous malignant melanoma [J].
Busam, KJ ;
Chen, YT ;
Old, LJ ;
Stockert, E ;
Iversen, K ;
Coplan, KA ;
Rosai, J ;
Barnhill, RL ;
Jungbluth, AA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1998, 22 (08) :976-982
[8]   Serological analysis of Melan-A(MART-1), a melanocyte-specific protein homogeneously expressed in human melanomas [J].
Chen, YT ;
Stockert, E ;
Jungbluth, A ;
Tsang, SL ;
Coplan, KA ;
Scanlan, MJ ;
Old, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :5915-5919
[9]   MART-1 is expressed less frequently on circulating melanoma cells in patients who develop distant compared with locoregional metastases [J].
Curry, BJ ;
Myers, K ;
Hersey, P .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (08) :2562-2571
[10]  
deVries TJ, 1997, CANCER RES, V57, P3223