Differential expression patterns of metastasis suppressor proteins in basal cell carcinoma
Date
2015Source Title
International Journal of Dermatology
Print ISSN
0011-9059
Publisher
Wiley-Blackwell Publishing Ltd.
Volume
54
Issue
8
Pages
905 - 915
Language
English
Type
ArticleItem Usage Stats
203
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views
305
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Abstract
Background: Basal cell carcinomas (BCCs) are common malignant skin tumors. Despite having a significant invasion capacity, they metastasize only rarely. Our aim in this study was to detect the expression patterns of the NM23-H1, NDRG1, E-cadherin, RHOGDI2, CD82/KAI1, MKK4, and AKAP12 metastasis suppressor proteins in BCCs. Methods: A total of 96 BCC and 10 normal skin samples were included for the immunohistochemical study. Eleven frozen BCC samples were also studied by quantitative real time polymerase chain reaction (qRT-PCR) to detect the gene expression profile. Results: NM23-H1 was strongly and diffusely expressed in all types of BCC. Significant cytoplasmic expression of NDRG1 and E-cadherin was also detected. However, AKAP12 and CD82/KAI1 expression was significantly decreased. The expressions of the other proteins were somewhere between the two extremes. Similarly, qRT-PCR analysis showed down-regulation of AKAP12 and up-regulation of NM23-H1 and NDRG1 in BCC. Morphologically aggressive BCCs showed significantly higher cytoplasmic NDRG1 expression scores and lower CD82/KAI1 scores than non-aggressive BCCs. Conclusion: The relatively preserved levels of NM23-H1, NDRG1, and E-cadherin proteins may have a positive effect on the non-metastasizing features of these tumors.
Keywords
AKAP12 proteinCD82 antigen
Metastasis suppressor protein
Mitogen activated protein kinase kinase 4
N myc downstream regulated I protein
Nucleoside diphosphate kinase A
Protein
Rho guanine nucleotide dissociation inhibitor 2
Unclassified drug
Uvomorulin
Aged
Article
Basal cell carcinoma
Controlled study
Down regulation
Female
Gene expression profiling
Human
Human tissue
Immunohistochemistry
Major clinical study
Male
Protein expression
Reverse transcription polymerase chain reaction
Upregulation
Permalink
http://hdl.handle.net/11693/22891Published Version (Please cite this version)
http://dx.doi.org/10.1111/ijd.12581Collections
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