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七种犬黑色素瘤细胞系及29例犬黑色素瘤回顾性病例中S100a、波形蛋白、神经元特异性烯醇化酶和黑色素A/MART-1的表达

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

作者信息

Koenig A, Wojcieszyn J, Weeks B R, Modiano J F

机构信息

Department of Small Animal Medicine and Surgery, College of Veterinary Medicine, Texas A&M University, College Station, USA.

出版信息

Vet Pathol. 2001 Jul;38(4):427-35. doi: 10.1354/vp.38-4-427.

Abstract

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. S 100a 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.

摘要

我们评估了波形蛋白、S100a和黑色素A/MART-1(T细胞识别的黑色素瘤抗原1)在从患有犬黑色素瘤的犬只中独立建立的7种细胞系中的表达情况。我们还将29例黑色素瘤病例临床标本中波形蛋白、S100a和神经元特异性烯醇化酶(NSE)的常规免疫染色与黑色素A/MART-1染色进行了比较,作为诊断指标的一部分。所有细胞系波形蛋白和S-100a表达均为阳性。黑色素A/MART-1表达仅在7种细胞系中的2种中持续可见。黑色素A/MART-1染色在黑色素沉着严重区域附近最为强烈。除1例临床标本外,所有标本波形蛋白染色均为阳性。S100a在大多数色素沉着性肿瘤(15/20,75%)和无色素性肿瘤(8/9,88.8%)中均有表达。29例肿瘤中有17例(58.6%)NSE染色为阳性。黑色素A/MART-1在18/29(62%)例肿瘤中表达,包括90%的色素沉着性肿瘤,但无色素性肿瘤均未表达。黑色素A/MART-1染色强度与生物学行为呈正相关,7例恶性肿瘤染色为阴性至弱阳性,10例良性肿瘤染色为中度至强阳性。3例恶性肿瘤黑色素A/MART-1染色为中度至强阳性。我们的结果表明,黑色素A/MART-1在培养细胞系中的表达可能不稳定。评估S100a和黑色素A/MART-1的表达有助于确诊犬黑色素瘤,黑色素A/MART-1可能对这些肿瘤的生物学行为具有特别的诊断价值。

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