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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Human high molecular weight-melanoma-associated antigen: utility for detection of metastatic melanoma in sentinel lymph nodes.
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Human high molecular weight-melanoma-associated antigen: utility for detection of metastatic melanoma in sentinel lymph nodes.

机译:人高分子量黑素瘤相关抗原:用于检测前哨淋巴结中转移性黑素瘤的实用程序。

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PURPOSE: Detection of micrometastasis in melanoma-draining lymph nodes is important for staging and prognosis. Immunohistochemical staining (IHC) using S-100p-HMB-45-, and MART-1-specfic antibodies is used for detecting metastases in sentinel lymph nodes (SLN). However, improvement in IHC is needed for melanoma micrometastasis detection. EXPERIMENTAL DESIGN: Paraffin-embedded archival tissue (PEAT) specimens were obtained from 42 non-SLN macrometastases, 42 SLN metastases, and 16 tumor-negative SLNs of 100 melanoma patients who underwent SLN biopsy. PEAT specimens were assessed by IHC with high molecular weight-melanoma-associated antigen (HMW-MAA)-specific monoclonal antibodies (mAb) and with S-100p-, HMB-45-, and MART-1-specific antibodies. Quantitative real-time reverse-transcriptase PCR assay was used for HMW-MAA and MART-1 mRNA detection. RESULTS: Expression frequency and immunostaining intensity were higher for HMW-MAA than MART-1 in nodal macrometastases (P < 0.0001 and P < 0.0001, respectively)and micrometastases (P < 0.0001 and P = 0.004, respectively). All 52 (100%) macrometastases were positive with HMW-MAA-specific mAbs, whereas 43 (83%) were positive with MART-1-specific mAbs. In a comparison analysis, 23 of 23 (100%) micrometastases were HMW-MAA-positive, whereas 21 (91%) and 18 (78%) specimens were S-100p- and HMB-45-positive, respectively. Quantitative real-time reverse-transcriptase PCR analysis of 48 nodal metastases showed HMW-MAA mRNA detection in SLNs with metastases. CONCLUSIONS: HMW-MAA is more sensitive and specific than MART-1, S-100p, and HMB-45 for IHC-based detection of SLN micrometastases. SLN PEAT-based detection specificity of melanoma micrometastases can be improved by IHC with HMW-MAA-specific mAbs.
机译:目的:检测引流黑色素瘤的淋巴结中的微转移对于分期和预后至关重要。使用S-100p-HMB-45-和MART-1-特异性抗体的免疫组化染色(IHC)用于检测前哨淋巴结(SLN)中的转移。但是,黑色素瘤微转移检测需要改善IHC。实验设计:石蜡包埋的档案组织(PEAT)标本取自100例行SLN活检的黑色素瘤患者的42例非SLN宏观转移,42例SLN转移和16例肿瘤阴性的SLN。通过IHC用高分子量黑素瘤相关抗原(HMW-MAA)特异性单克隆抗体(mAb)以及S-100p,HMB-45-和MART-1特异性抗体评估PEAT标本。实时定量逆转录酶PCR法用于HMW-MAA和MART-1 mRNA检测。结果:HMW-MAA在淋巴结大转移(分别为P <0.0001和P <0.0001)和微小转移(分别为P <0.0001和P = 0.004)中的表达频率和免疫染色强度均高于MART-1。 HMW-MAA特异性mAb全部52(100%)个宏观转移阳性,而MART-1特异性mAb全部43(83%)阳性。在比较分析中,23个微转移中有23个(100%)HMW-MAA阳性,而S-100p和HMB-45阳性的标本分别为21个(91%)和18个(78%)。实时定量逆转录酶PCR分析48个淋巴结转移显示SLNs中有转移的HMW-MAA mRNA检测。结论:对于基于IHC的SLN微转移检测,HMW-MAA比MART-1,S-100p和HMB-45更为灵敏和特异。 IHC和HMW-MAA特异性mAb可以改善基于SLN PEAT的黑色素瘤微转移的检测特异性。

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