» Articles » PMID: 24587914

P16 Expression Is Lost in Severely Atypical Cellular Blue Nevi and Melanoma Compared to Conventional, Mildly, and Moderately Atypical Cellular Blue Nevi

Overview
Journal ISRN Dermatol
Specialty Dermatology
Date 2014 Mar 4
PMID 24587914
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Background. Significant decreases in p16 expression have been shown to occur in melanoma compared to Spitz tumors, and loss of p16 staining has been found to correlate with melanoma tumor progression. However, comparison of p16 between atypical cellular blue nevi (CBN) and melanoma has not been reported previously. Methods. p16 immunohistochemical staining was evaluated in 14 atypical CBN, 8 conventional and atypical melanocytic nevi, and 16 melanomas, including 4 malignant CBN. p16 staining intensity was graded on a scale of 0-3 and the percentage of melanocytes stained with p16 was determined. Results. p16 staining was significantly higher in all CBN as a group when compared to melanomas (P = 0.001) and malignant CBN (P = 0.00008). Higher p16 expression was also seen in mildly (P = 0.0002) and moderately atypical (P = 0.02), but not severely atypical, CBN compared to melanomas. Conclusions. p16 immunohistochemical expression is higher in mildly and moderately atypical CBN compared to severely atypical CBN and melanomas. In conjunction with additional markers and histology, p16 staining may be useful in confirming the benign nature of these tumors, but is not useful in distinguishing severely atypical CBN from malignant cases, consistent with the overlapping histologic features between these tumors.

Citing Articles

Cellular Blue Nevus Diagnosed following Excision of Melanoma: A Challenge in Diagnosis.

Jonjic N, Dekanic A, Glavan N, Prpic-Massari L, Grahovac B Case Rep Pathol. 2016; 2016:8107671.

PMID: 27313934 PMC: 4899595. DOI: 10.1155/2016/8107671.


Immune-phenotypical markers for the differential diagnosis of melanocytic lesions.

Botti G, Marra L, Anniciello A, Scognamiglio G, Gigantino V, Cantile M Int J Clin Exp Pathol. 2015; 8(9):9742-51.

PMID: 26617684 PMC: 4637769.


A p16-Ki-67-HMB45 immunohistochemistry scoring system as an ancillary diagnostic tool in the diagnosis of melanoma.

Uguen A, Talagas M, Costa S, Duigou S, Bouvier S, De Braekeleer M Diagn Pathol. 2015; 10:195.

PMID: 26503349 PMC: 4623282. DOI: 10.1186/s13000-015-0431-9.


Epigenetic effects of cadmium in cancer: focus on melanoma.

Venza M, Visalli M, Biondo C, Oteri R, Agliano F, Morabito S Curr Genomics. 2015; 15(6):420-35.

PMID: 25646071 PMC: 4311387. DOI: 10.2174/138920291506150106145932.

References
1.
Soares de Sa B, Fugimori M, Ribeiro K, Duprat Neto J, Neves R, Landman G . Proteins involved in pRb and p53 pathways are differentially expressed in thin and thick superficial spreading melanomas. Melanoma Res. 2009; 19(3):135-41. DOI: 10.1097/CMR.0b013e32831993f3. View

2.
Talve L, Sauroja I, Collan Y, Punnonen K, Ekfors T . Loss of expression of the p16INK4/CDKN2 gene in cutaneous malignant melanoma correlates with tumor cell proliferation and invasive stage. Int J Cancer. 1997; 74(3):255-9. DOI: 10.1002/(sici)1097-0215(19970620)74:3<255::aid-ijc4>3.0.co;2-y. View

3.
Al Dhaybi R, Agoumi M, Gagne I, McCuaig C, Powell J, Kokta V . p16 expression: a marker of differentiation between childhood malignant melanomas and Spitz nevi. J Am Acad Dermatol. 2011; 65(2):357-363. DOI: 10.1016/j.jaad.2010.07.031. View

4.
Ruiter D, van Dijk M, Ferrier C . Current diagnostic problems in melanoma pathology. Semin Cutan Med Surg. 2003; 22(1):33-41. DOI: 10.1053/sder.2003.50003. View

5.
Stefanaki C, Stefanaki K, Antoniou C, Argyrakos T, Stratigos A, Patereli A . G1 cell cycle regulators in congenital melanocytic nevi. Comparison with acquired nevi and melanomas. J Cutan Pathol. 2008; 35(9):799-808. DOI: 10.1111/j.1600-0560.2007.00912.x. View