Potential diagnostic utility of PRAME and p16 immunohistochemistry in melanocytic nevi and malignant melanoma

被引:11
作者
Bahmad, Hisham F. [1 ]
Oh, Kei Shing [1 ]
Alexis, John [1 ,2 ]
机构
[1] Mt Sinai Med Ctr, Arkadi M Rywlin MD Dept Pathol & Lab Med, 4300 Alton Rd, Miami Beach, FL 33140 USA
[2] Florida Int Univ, Herbert Wertheim Coll Med, Dept Pathol, Miami Beach, FL USA
关键词
diagnostic biomarker; malignant melanoma; melanocytic nevus; p16; PRAME; GENE-EXPRESSION SIGNATURE; ANTIGEN PRAME; CANCER; MUTATIONS; PROGNOSIS; NY-ESO-1;
D O I
10.1111/cup.14438
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background PRAME (PReferentially expressed Antigen in MElanoma) is a tumor-associated antigen that has been studied in various cutaneous melanocytic lesions. p16, on the other hand, has been proposed to aid in distinguishing between benign and malignant melanocytic neoplasms. Studies on the diagnostic utility of PRAME and p16 in combination in differentiating nevi from melanoma are limited. We aimed to assess the diagnostic utility of PRAME and p16 in melanocytic tumors and their role in distinguishing between malignant melanomas and melanocytic nevi. Methods This is a single-center retrospective cohort analysis over a 4-year period (2017-2020). We used the pathological database of malignant melanomas (77 cases) and melanocytic nevi (51 cases) specimens from patients who underwent shave/punch biopsies or surgical excisions and evaluated immunohistochemical staining percentage positivity and intensity for PRAME and p16. Results Most malignant melanomas showed positive/diffuse PRAME expression (89.6%); on the other hand, 96.1% of nevi did not express PRAME diffusely. p16 was expressed consistently in nevi (98.0%). However, p16 expression in malignant melanoma was infrequent in our study. PRAME had a sensitivity and specificity of 89.6% and 96.1%, respectively, for melanomas versus nevi; on the other hand, p16 had a sensitivity and specificity of 98.0% and 28.6%, respectively, for nevi versus melanoma. Also, a PRAME+/p16- melanocytic lesion is unlikely to be a nevus where most nevi were PRAME-/p16+. Conclusion In conclusion, we confirm the potential utility of PRAME and p16 for distinguishing melanocytic nevi from malignant melanomas.
引用
收藏
页码:763 / 772
页数:10
相关论文
共 44 条
  • [1] Use of p16 immunohistochemical stain to help differentiate inflamed melanocytic nevi from metastatic melanoma in the setting of immunotherapy
    Adelman, Madeline
    Lyons, Alexis B.
    Seale, Lauren
    Friedman, Ben J.
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2020, 82 (04) : E117 - E119
  • [2] Cancer Testis Antigens and Immunotherapy: Expression of PRAME Is Associated with Prognosis in Soft Tissue Sarcoma
    Albertsmeier, Markus
    Altendorf-Hofmann, Annelore
    Lindner, Lars H.
    Issels, Rolf D.
    Kampmann, Eric
    Duerr, Hans-Roland
    Schubert-Fritschle, Gabriele
    Angele, Martin K.
    Kirchner, Thomas
    Jungbluth, Achim A.
    Knoesel, Thomas
    [J]. CANCERS, 2020, 12 (12) : 1 - 13
  • [3] Immunohistochemical expression of p16 in desmoplastic melanoma
    Blokhin, Elena
    Pulitzer, Melissa
    Busam, Klaus J.
    [J]. JOURNAL OF CUTANEOUS PATHOLOGY, 2013, 40 (09) : 796 - 800
  • [4] Gene Expression Profiling and PRAME Status Versus Tumor-Node-Metastasis Staging for Prognostication in Uveal Melanoma
    Cai, Louis
    Paez-Escamilla, Manuel
    Walter, Scott D.
    Tarlan, Bercin
    Decatur, Christina L.
    Perez, Barbara M.
    Harbour, J. William
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 2018, 195 : 154 - 160
  • [5] PRAME Immunoexpression in 275 Cutaneous Melanocytic Lesions: A Double Institutional Experience
    Cazzato, Gerardo
    Cascardi, Eliano
    Colagrande, Anna
    Belsito, Vincenzo
    Lospalluti, Lucia
    Foti, Caterina
    Arezzo, Francesca
    Dellino, Miriam
    Casatta, Nadia
    Lupo, Carmelo
    Buongiorno, Luigi
    Stellacci, Alessandra
    Marrone, Maricla
    Ingravallo, Giuseppe
    Maiorano, Eugenio
    Resta, Leonardo
    [J]. DIAGNOSTICS, 2022, 12 (09)
  • [6] Chang L. M., 2014, ISRN DERMATOL, V2014
  • [7] Melanoma genetics and the development of rational therapeutics
    Chudnovsky, Y
    Khavari, PA
    Adams, AE
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (04) : 813 - 824
  • [8] An Independent Validation of a Gene Expression Signature to Differentiate Malignant Melanoma From Benign Melanocytic Nevi
    Clarke, Loren E.
    Flake, Darl D., II
    Busam, Klaus
    Cockerell, Clay
    Helm, Klaus
    McNiff, Jennifer
    Reed, Jon
    Tschen, Jaime
    Kim, Jinah
    Barnhill, Raymond
    Elenitsas, Rosalie
    Prieto, Victor G.
    Nelson, Jonathan
    Kimbrell, Hillary
    Kolquist, Kathryn A.
    Brown, Krystal L.
    Warf, M. Bryan
    Roa, Benjamin B.
    Wenstrup, Richard J.
    [J]. CANCER, 2017, 123 (04) : 617 - 628
  • [9] Towards diagnostic criteria for malignant deep penetrating melanocytic tumors using single nucleotide polymorphism array and next-generation sequencing
    Ebbelaar, Chiel F.
    Schrader, Anne M. R.
    van Dijk, Marijke
    Meijers, Ruud W. J.
    de Leng, Wendy W. J.
    Bloem, Lourens T.
    Jansen, Anne M. L.
    Blokx, Willeke A. M.
    [J]. MODERN PATHOLOGY, 2022, 35 (08) : 1110 - 1120
  • [10] Immunotype and Immunohistologic Characteristics of Tumor-Infiltrating Immune Cells Are Associated with Clinical Outcome in Metastatic Melanoma
    Erdag, Gulsun
    Schaefer, Jochen T.
    Smolkin, Mark E.
    Deacon, Donna H.
    Shea, Sofia M.
    Dengel, Lynn T.
    Patterson, James W.
    Slingluff, Craig L., Jr.
    [J]. CANCER RESEARCH, 2012, 72 (05) : 1070 - 1080