Expression of Tissue Markers in Malignant and Benign Melanocytic Proliferations - a Comparative Study

被引:0
作者
Ungureanu, Loredana [1 ]
Grigore, Lavinia [1 ]
Balacescu, Loredana [2 ]
Berindan-Neagoe, Ioana [2 ]
Cosgarea, Rodica M. [1 ]
Balacescu, Ovidiu [2 ]
机构
[1] Iuliu Hatieganu Univ Med & Pharm, Dept Dermatol, Cluj Napoca, Romania
[2] Oncol Inst Prof Dr Ion Chiricuta, Dept Funct Gen Prote & Expt Pathol, 34-36 Republicii St, Cluj Napoca 400015, Romania
来源
ROMANIAN BIOTECHNOLOGICAL LETTERS | 2016年 / 21卷 / 02期
关键词
melanocytic lesions; CYR61; GDF15; KRT18; BCL2; DIFFERENTIATION FACTOR 15; MELANOMA; CANCER; GENES; IDENTIFICATION; CCN1;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background The most efficient treatment for cutaneous melanoma is surgical excision in its early stage, which involves an accurate differentiation between melanoma and atypical nevi. Objectives The aim of this study was to investigate the expression of GDF15, CYR61, KRT18 and BCL-2 in cutaneous melanoma, atypical nevi and common nevi and to assess their possible role in differentiating malignant and benign lesions. Material and Methods Tissues samples from 13 invasive cutaneous melanomas, 11 dysplastic nevi and 14 common nevi as well as ten normal skin tissue samples were used for gene expression analysis. Light Cycler 480 (Roche Technologies) and Delta Delta Ct methodwas used to evaluate the expression of genes of interest. Results Gene CYR 61 proved to be down-regulated in cutaneous melanoma and common melanocytic nevi and up-regulated in dysplastic melanocytic nevi. GDF15 expression is progressively up-regulated from common nevi to dysplastic nevi and melanoma. KRT18 is down-regulated in common nevi and melanoma, and is slightly up-regulated in dysplastic nevi. BCL2 expression is progressively down-regulated from common nevi to dysplastic nevi and melanoma. Conclusions GDF15 could represent an important factor for melanoma progression and for differential diagnosis. CYR61 seems to be an early marker of neoplasia, but its capacity to distinguish benign lesions from early malignant ones has to be tested on larger studies that also include in situ lesions. BCL2 does not seem to specifically contribute to differentiating benign lesions from malignant ones. KRT 18 could play a role in cell proliferation and distinguishing typical lesions from dysplastic ones.
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页码:11365 / 11371
页数:7
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