评估恶性黑色素瘤、发育不良痣和普通痣中 MMP-9、MMP-13、MMP-21 和 TIMP-1 的表达。

Northern clinics of Istanbul Pub Date : 2024-04-25 eCollection Date: 2024-01-01 DOI:10.14744/nci.2023.69009
Meryem Yuvruk, Rabia Burcin Girgin, Ebru Zemheri
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引用次数: 0

摘要

研究目的虽然MMPs在黑色素瘤发病机制中的作用已众所周知,但很少有研究调查它们在痣和发育不良痣的发病中的作用。本研究旨在探讨 MMP-9、MMP-13、MMP-21 和 TIMP-1 在恶性黑色素瘤(MM)、皮内痣(IDN)和发育不良痣(DN)中的表达差异:方法:对2013年至2014年间本院病理门诊档案中的60例病例的MMP-9、MMP-13、MMP-21和TIMP-1抗体进行免疫组化研究:MM组的MMP-9表达比例和强度最高(P0.05)。与 IDN 相比,DN 和 MM 组的 MMP-21 病变染色强度有统计学意义(分别为 p=0.001 和 p=0.011)。就 TIMP-1 而言,IDN 组和 MM 组病变细胞的染色比例差异显著(p 结论:当病变无法区分时,以下标记物可能会有所帮助;在 MM 和 IDN 无法区分的病例中,病变细胞和基质细胞中 MMP-9 染色比例和强度的增加有利于 MM。在病理学家无法区分DN和MM的病例中,病变细胞中MMP-13染色比例的增加有利于DN。在 DN 和 IDN 无法区分的情况下,病变细胞强烈表达的 MMP-21 可作为评估病变的潜在标志物,有利于 DN。如果病变细胞中 TIMP-1 的表达强度较高,则在 DN 和 MM 难以区分的病例中会更倾向于 DN。在无法区分 MM 和 DN 的病例中,TIMP-1 在基质细胞中的高表达比例和高表达强度可能有利于 MM。
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Evaluation of MMP-9, MMP-13, MMP-21, and TIMP-1 expressions in malign melanom, dysplastic nevi, and banal nevi.

Objective: Although the role of MMPs in the pathogenesis of melanoma is known, few studies have investigated their role in the development of nevi and dysplastic nevi. This study aims to search the expression differences of MMP-9, MMP-13, MMP-21, and TIMP-1 between malignant melanoma (MM), intradermal nevi (IDN), and dysplastic nevi (DN).

Methods: MMP-9, MMP-13, MMP-21, and TIMP-1 antibodies were studied immunohistochemically for 60 cases in our pathology clinic archive between 2013 and 2014.

Results: The MM group had the highest expression percentage and intensity for MMP-9 (p<0.001). There was no statistical significance between MMP-13 expression intensities of lesion cells and stromal cells and stromal expression intensities (p>0.05). MMP-21 lesion staining intensities in DN and MM compared to IDN were statistically significant (p=0.001, p=0.011, respectively). For TIMP-1, there was a significant difference between the IDN and the MM group regarding the staining proportion of lesion cells (p<0.01). There was a statistically significant difference in all groups according to lesion cells' expression intensity. (IDN-DN p<0.001, IDN-MM p=0.044, DN-MM p<0.001).

Conclusion: The following markers can be helpful when lesions cannot be differentiated; increased staining proportions and intensity of MMP-9 in both lesion and stromal cells favor MM in cases where MM and IDN cannot be differentiated. The increased MMP-13 staining proportion of lesion cells can favor DN in cases where the pathologist cannot differentiate DN and MM. Intense expression of MMP-21 by lesion cells can be a potential marker for evaluating the lesion in favor of DN in cases where DN and IDN cannot be differentiated. The high expression intensity of TIMP-1 in lesion cells can favor DN in cases where there is ambiguity between DN and MM. High expression proportion and intensity of stromal cells of TIMP-1 can be useable in favor of MM in cases where MM and DN cannot be differentiated.

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