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Nuclear to non-nuclear Pmel17/gp100 expression (HMB45 staining) as a discriminator between benign and malignant melanocytic lesions

机译:核到非核的Pmel17 / gp100表达(HMB45染色)可作为良性和恶性黑素细胞病变的鉴别指标

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摘要

HMB45 is a mouse monoclonal antibody raised against Pmel17/gp100, a melanoma-specific marker, which is routinely used in the diagnosis of primary cutaneous malignant melanoma. The standard expression pattern for a positive HMB45 staining result on immunohistochemistry is based upon the results of chromogenic-based methods. We re-evaluated patterns of HMB45 staining across the 480-core “SPORE melanoma progression array” containing lesions representing the spectrum of melanocytic lesions ranging from thin nevus to visceral metastasis using the fluorescence-based staining technique and Automated Quantitative Analysis (AQUA) of the obtained digital images. The methods validated the expected cytoplasmic HMB45 staining pattern in 70/108 malignant lesions and in the epithelial components of nevus specimens. However, the fluorescence-based approach revealed a nuclear HMB45 localization present in the dermal component of all nevi that was not seen before. This nuclear localization could not be observed on routine chromogenic stains because the standard hematoxylin nuclear counterstain overwhelms the weak nuclear HMB45 stain. The thin (0.450±0.253) and thick (0.513±0.227) nevi had strongly positive mean ln(nuclearon-nuclear AQUA score ratios), which are significantly higher than those from the group of malignant lesions (p<0.0001). This finding was reproduced on a smaller but independent progression array composed of nevi and melanomas from the Yale Pathology archives (p<0.01). The odds ratio associated with a sample being a nevus was 2.24 (95% CI: 1.87-2.69, p<0.0001) for each 0.1 unit increase of the ln(nuclearon-nuclear AQUA score ratio) to yield an ROC curve with 0.93 units of area and a simultaneously maximized sensitivity of 0.92 and specificity of 0.80 for distinguishing benign nevi from malignant melanomas. Based on this preliminary study, we propose that the ratio of nuclear to non-nuclear HMB45 staining may be useful for diagnostic challenges in melanocytic lesions.
机译:HMB45是针对Pmel17 / gp100(一种黑色素瘤特异性标志物)产生的小鼠单克隆抗体,通常用于诊断原发性皮肤恶性黑色素瘤。免疫组化显示HMB45染色阳性的标准表达模式基于基于生色方法的结果。我们使用基于荧光的染色技术和自动定量分析(AQUA),对480核“ SPORE黑色素瘤进展阵列”上的HMB45染色模式进行了重新评估,该阵列包含代表从薄痣到内脏转移的黑素细胞病变范围的病变。获得数字图像。该方法验证了在70/108个恶性病变和痣标本的上皮成分中预期的细胞质HMB45染色模式。然而,基于荧光的方法揭示了在所有痣的真皮成分中均存在的核HMB45定位,这是以前从未见过的。在常规发色染料上无法观察到这种核定位,因为标准的苏木精核复染压倒了弱核HMB45染料。薄的(0.450±0.253)和厚的(0.513±0.227)痣平均ln(核/非核AQUA评分比)强烈阳性,显着高于恶性病变组(p <0.0001)。该发现在耶鲁病理学档案中由痣和黑色素瘤组成的较小但独立的进展阵列上再现(p <0.01)。 ln的每增加0.1个单位(核/非核AQUA得分比),与痣相关的比值比为2.24(95%CI:1.87-2.69,p <0.0001),得出ROC曲线为0.93单位面积,同时最大灵敏度为0.92,特异度为0.80,用于区分良性痣和恶性黑色素瘤。基于此初步研究,我们建议核与非核HMB45染色的比例可能有助于诊断黑素细胞病变。

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