International Journal of Dermatology · 2014 · 13 citations · 37 references
MedicineDermatologyPathologyCutaneous OncologyMetastasisMolecular OncologyBasal Cell CarcinomaCancer BiomarkersCancer Molecular PathologySkin TumorsTumor MarkersTumor Suppressor GenesDifferential Transcript ExpressionImmunohistochemical BiomarkersImmunohistochemical DetectionImmunohistochemical MarkersImmunohistochemical StainingMarker Expression PatternsMetastatic Basal Cell CarcinomaSkin Tumor Immunohistochemistry
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.
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McCarty Ks, Éva Szabó, Flowers Jl et al. · PubMed · 1986 · 422 citations
Medicine, Endocrinology, Oncology +17
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Sucharita Bandyopadhyay, Sudha K. Pai, Shigeru Hirota et al. · Oncogene · 2004 · 197 citations