• https://theoejwilson.com/
  • santuy4d
  • mariatogel
  • santuy4d
  • garuda slot
  • garudaslot
  • https://edujournals.net/
  • nadimtogel
  • https://mitrasehatjurnal.com/
  • slot gacor hari ini
  • g200m
  • https://perpustakaan.stpreinha.ac.id/mahasiswa/
  • https://www.lml.stpreinha.ac.id/lab/
  • https://cursosvirtuales.icip.edu.pe/nice/
  • slot resmi
  • HUBUNGAN TINGKAT EKSPRESI P15 TERHADAP NEVUS MELANOSITIK DAN MELANOMA MALIGNA | Nasution | Jurnal Kedokteran dan Kesehatan : Publikasi Ilmiah Fakultas Kedokteran Universitas Sriwijaya

    HUBUNGAN TINGKAT EKSPRESI P15 TERHADAP NEVUS MELANOSITIK DAN MELANOMA MALIGNA

    Renny Apliza Nasution, Ika Kartika, Theodorus Theodorus

    Abstract


     Lesi melanositik memiliki gambaran morfologi dan sitomorfologi yang luas mencakup lesi jinak yaitu nevus melanositik dan lesi ganas yaitu melanoma maligna. Beberapa gambaran nevus melanositik menyerupai melanoma. p15 merupakan gen penekan tumor dan biomarker yang kuat sehingga dapat digunakan untuk membedakan antara nevus dan melanoma. Tujuan penelitian ini adalah mengetahui hubungan tingkat ekspresi p15 pada nevus dan melanoma.  Penelitian ini merupakan penelitian deskriptif observasional dengan desain serial kasus sejak 1 Januari 2015 sampai 30 Desember 2019. Sebanyak 60 sampel dilakukan pemeriksaan imunohistokimia menggunakan antibodi p15. Ekspresi p15 dinilai berdasarkan proporsi sel tumor yang terpulas dan intensitas pulasan. Analisis statistik menggunakan SPSS versi 23.0. Hasil penelitian menunjukkan bahwa nevus melanositik paling bnayk dijumpai pada perempuan (76,7%), pada kelompok usia <55 tahun (90%), lokasi tumor pada kepala dan leher (83,3) dan pada tipe histopatologi dermal naevus (53,3%). Melanoma maligna paling banyak ditemukan pada jenis kelamin laki-laki (53,6%), pada kelompok usia <55 tahun (57,1%), lokasi tumor pada kepala dan leher (35,7%) dan pada tipe histopatologi nodular melanoma (42,9%). Terdapat hubungan bermakna antara tingkat ekspresi p15 dengan lesi melanositik (nevus melanositik dan melanoma maligna) (r=0,9666; p=0,000). Ekspresi p15 tinggi dijumpai pada nevus melanositik dan rendah pada melanoma maligna. Terdapat hubungan bermakna antara tingkat ekspresi p15 dengan lesi melanositik (nevus melanositik dan melanoma maligna). Semakin rendah ekspresi p15 maka semakin besar kemungkinan terjadi melanoma maligna.

     

    Background. Melanocytic lesions have a broad morphological and cytomorphological picture including benign conditions or melanocytic naevus and malignant melanoma. Some features of a melanocytic nevus mimicking melanoma. p15 is a tumor suppressor gene and is a robust biomarker that can be used to differentiate between nevus and melanoma. This study aims to determine the correlation between p15 expression in melanocytic naevus and malignant melanoma. Methods. This research is an observational descriptive study with a case series design, conducted from January 1st, 2015 to December 30th 2019. A total of 60 samples were subjected to immunohistochemical examinations using antibody p15. The expression p15 is based on tumor cell proportion and intensity. Statistical analysis using SPSS version 23. Result. Melanocytic nevus was predominantly female (76.7%), age group <55 years (90%), location of tumors on the head and neck (83.3), histopathological type of dermal naevus (53.3%). Malignant melanoma was mostly found in men (15, 53.6%), age group <55 years (57.1%), the location of tumors on the head and neck (35.7%), type histopathology of nodular melanoma (42.9%). The correlation between p15 level expression and melanocytic lesions (melanocytic nevus and malignant melanoma) (r = 0.9666; p = 0.000). Conclusion. High expression of p15 was found in melanocytic nevus and low in malignant melanoma. There was correlation between p15 level expression and melanocytic lesions (melanocytic nevus and malignant melanoma). The lower the p15 expression, the more likely malignant melanoma will occur.


    Full Text:

    PDF

    References


    Ghosh A, Ghartimagar D, Thapa S, Sathian B, Shrestha B, Talwar OP. Benign melanocytic nevi- A histomorphological analysis. J Pathol Nep 2018; 8(2): 1384-88.

    Bastian BC. The molecular pathology of melanoma: an integrated taxonomy of melanocytic neoplasia. Annu Rev Pathol Mech Dis 2014; 9: 239-71.

    Damsky WE, Bosenberg M. Melanocytic nevi and melanoma: unraveling a complex relationship. Onc 2017; 36(42): 5771-92.

    Shaughnessy M, Klebanov N, Tsao H. Clinical and therapeutic implications of melanoma genomics. J Transl Genet Genom 2018; 2(14): 1-13.

    Mulenga M, Montgomery ND, Chagomerana M, Mzumala T, Tomoka T, Kampani C et al. Epidemiological and histopathological profile of malignant melanoma in Malawi. BMC Clin Pathol 2019; 19(5): 1-6.

    Syaputri NA, Musa Z, Septadina IS. Karakteristik Histopatologi Melanoma Maligna di Bagian Patologi Anatomi RSUP Dr. Moh. Hoesin Palembang Tahun 2009-2013. Biomedical Journal of Indonesia: Jurnal Biomedik Fakultas Kedokteran Universitas Sriwijaya 2018; 4(1): 26-32.

    Bogenrieder T, Herlyn M. The molecular pathology of cutaneous melanoma. Cancer Biomark 2010; 9(1-6): 267-86.

    Bsirini C, Somller BR. Histologic mimics of malignant melanoma. Singapore Med J 2018; 59(11): 602-7.

    Hale CS. Nevoid melanoma. PathologyOutlines.com website. http://www.pathologyoutlines.com/topic/skintumormelanocyticnevoidmelanoma.html. Last updated: 31 May 2020.

    Theodosiou G, Johansson I, Hamnerius L, Svensson A. Naevoid malignant melanoma: a diagnosis of a naevus that you later regret. Acta Derm Venereol 2017;97:745-6.

    Costa S, Byrne M, Pissaloux D, Haddad V, Paindavoine S, Thomas L et al. Melanomas associated with blue nevi or mimicking cellular blue nevi clinical, pathologic and molecular study of 11 cases displaying a high frequency of GNA11 mutations, BAP1 expression loss and a predilection for the scalp. Am J Surg Pathol 2016; 40(3): 368-77.

    Stephen S, Cassarino DS. Immunohistochemical expression of p16 in melanocytic lesion. an updated review and meta-analysis. Arch Pathol Lab Med 2018;142(7): 815-28.

    Feuerer L, Lamm S, Henz I, Kappelmann-Fenzl M, HaferkampS, Meierjohann S, Hellerbrand C, et al. Role of melanoma inhibitory activity in melanocyte senescence. Pigment Cell Melanoma Res. 2019;00:1-15

    El-Deiry WS. p21 (WAF1) mediates cell-cycle inhibition, relevant to cancer suppression and therapy. Cancer Res 2016;76(18):5189-91.

    Taylor LA, O’Day C, Dentchev T, Hood K, Chu EY, Ridky TW, Seykora JT. p15 expression differentiated nevus from melanoma. Amjpathol 2016; 186(12): 3094-99.

    Chicorek M, Wachulska M, Stasiewicz A, Tyminska A. Skin melanocytes: biology and development. Postep Derm Alergol 2013; 30(1): 30-41.

    D’Mello SAN, Finlay GJ, Baguley BC, Askarian-Amiri ME. Signaling pathways in melanogenesis. Int J Mol Sci. 2016;17:1-18.

    Kirkham N, Aljefri K. Tumors and cysts of the epidermis. In: Elder DE, Elenitsas R, Johnson BL, editors. Lever’s histopathology of the skin. 11th ed. Philadelphia: Wolters Kluwer. 2016. p699-705.

    Garza L. Developmental biology nof the skin. In: Kang S, Amagai M, Bruckner AL, Enk AH, Margolis DJ, McMichael AJ, Orringer JS, editors. Fitzpatrick’s Dermatology. New York: Mc Graw Hill Education. 2019. p49-61.

    Mescher AL. Junquiera’s Basic Histology Text and Atlas. 14th ed. New York: Mc Graw Hill Education; 2016. p371-92.

    Ross MH, Pawlina W. Histology a Text and Atlas. 6th ed. Philadelphia: Wolters Kluwer. 2011. p488-525.

    Tsaniah R, Aspitriani, Fatmawati. Prevalensi dan gambaran histopatologi nevus pigmentosus di bagian patologi anatomi Rumah Sakit Dr. Mohammad Hoesin Palembang Periode 1 Januari 2009-31 Desember. MKS 2015; 47( 2 ): p 2-5.

    Mufti ST, Falemban A, Rizwan Z. Clinicopathological features of melanocytic nevi and their correlation to cutaneous melanoma among patients attending King Abdulaziz University Hospital, Jeddah, Saudi Arabia. Sudan J Med Sci 2018; 13(2): 98-113.

    Ghosh A, Ghartimagar D, Thapa S, Sathian B, Shrestha Bm Talwar OP. Benign melanocytic lesions with emphasis on melanocytic nevi- A histomorphological analysis. J Pathol Nep 2018; 8: 1384-88.

    Alendar T, Kittler H. Morphologic characteristics of nevi associated with melanoma: a clinical, dermatoscopic and histopathologic analysis. Dermatol Pract Concept 2018; 8(2): 7.

    Barnhill R. Pathology of melanocytic nevi and melanoma 3rd Edition. USA: Springer; 2014. p 78-81.

    Gundalli S, Kadadavar S, Singhania S, Kolekar R. Histopathological spectrum of benign melanocytic nevi - our experience in a tertiary care. Our Dermato Online 2016; 7(1): 21-5.

    Elder DE, Barnhill RL, Bastian BC, Cook MG, Fouchardiere DL, Gerami P, et al. In: Elder DE, Massi D, Scolyer RA, Willemze R, editors. WHO Classification of tumours. IARC: Lyon; 2017. p 65-151.

    Elder DE, Elenitsas R, Murphy GF, Xu XO. Benign pigmented lesions and malignant melanoma. In: Elder DE, Elenitsas R, Johnson BL, editors. Lever’s histopathology of the skin. 11th ed. Philadelphia: Wolters Kluwer. 2016. P.235-40.

    Maghari A. Dysplastic (or atypical) nevis showing moderate or severe atypia with clear margins on the shave removal specimens are most likely completely excised. J Cutan Med Surg 2016; 21(1): 1-6.

    Salim S, Karima S, Kaoutar Z, Hassam B. Meyerson phenomenon simulating a halo nevus. Clin Med Img Lib 2018; 4(5):1-3.

    Flores AF. Eponyms, morphology, and pathogenesis of some less mentioned types of melanocytic nevi. Am J Dermatopathol 2012 ;34(6): 607–18.

    Castagna RD, Chemello RML, Stramari JM. The recurrent nevus phenomenon. An Bras Dermatol. 2017; 92(4): 531-33.

    King R, Hayzen BA, Page RN, Googe PB, Zeagler D, Mihm MC. Recurrent nevus phenomenon: a clinicopathologic study of 357 cases and histologic comparison with melanoma with regression. Mod Pathol 2009; 22: 611–17.

    Weedon D. Lentigines, nevi, and melanomas. In: Weedon D. Weedon’s skin pathology. 10th ed. Churchill Livingstone Elsevier: China; 2010. p 713-34.

    Dika E, Ravaioli GM, Fanti PA, Neri I, Patrizi A. Spitz nevi and other spitzoid neoplasms in children: Overview of incidence data and diagnostic criteria. Pediatr Dermatol 2017; 34(1): 25–32.

    Bloom & Fawcett. Buku ajar histologi. Edisi Ke-12. Jakarta: Penerbit Buku Kedokteran EGC; 1994. p 536-46.

    Ward WH, Lambreton F, Goel N, Yu JQ, Farma JM. Clinical presentation and staging of melanoma. In: Ward WH, Farma JM editors. Cutaneous melanoma etiology and therapy. 1th ed. Philadelphia: USA; 2017. p 79-88.

    Grichnik JM, Rhodes AR, Sober AJ. Benign neoplasia and hyperplasia of melanocytes. In: Goldsmith LA, Katz SI Gilchrest BA, Paller AS, Leffell DJ, Wolff K (eds). Fitzpatrick’s dermatology in general medicine. 8th ed. The McGraw-Hill Companies: USA; 2012. p 1377-416.

    Kumari M, Kaushik ML. Comprehensive study to decline the burden of skin cancer. Int J Pharm Sci Drugs Res 2018; 10(3): 111-17

    Lazar AJ, Murphy GF. The Skin. In: Kumar V, Abbas AK, Aster JC, editors. Robbins and Cotran pathology basis of disease. 9th ed. Philadelphia: Elsevier Saunders; 2015. p 1147-49.

    Pizzichetta MA, Massi D, Mandala M, Queirolo P, StanganelliI, Giorgi VD, et al. Clinicopathological predictors of recurrence in nodular and superficial spreading cutaneous melanoma: a multivariate analysis of 214 cases. J Transl Med 2017; 15(1): 227.

    Mar V, Roberts H, Wolfe R, English DR, Kelly JW. Nodular Melanoma: A distinct clinical entity and the largest contributor to melanoma deaths in Victoria, Australia. J Am Achad dermatol 2013; 68(4): 568-75.

    Leonardi GC, Falzone L, Salemi R, Zanghi A, Spandidos DA, McCubrey JA et al. Cutaneous melanoma: From pathogenesis to therapy (review). Int J Oncol 2018; 52(4): 1071-80.

    Mar V, Roberts H, Wolfe R, English DR, Kelly JW. Nodular Melanoma: A distinct clinical entity and the largest contributor to melanoma deaths in Victoria, Australia. J Am Achad dermatol 2013; 68(4): 568-75.

    Joanna F, Linda W, Juraj B. CDKN2B (cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)). Atlas of Genetics and Cytogenetics in Oncology and Haematology. 2011; 15(8): 652-57

    Vermeulen K, Berneman, ZN, Van Bockstaele DR. Cell cy gulation K. Vermeulen et al. The cell cycle: a review of regulation, deregulation and therapeutic targets in cancercle and apoptosis. Cell Prolif 2003; 36(3): 131-49.

    Furney SJ, Turajilic S, Stamp G, Nohadani M, Carlisle A, Thomas M et al. Genome sequencing of mucosal melanomas reveals that they are driven by distinct mechanisms from cutaneous melanoma. J Pathol 2013; 230(3): 261–69.

    Lynda C, Glenn M, Ronald A. Malignant melanoma: modern black plague and genetic black box. Genes dev 2018; 12(22): 3467-81.

    Yasuhiro M, Chikako N, Takashi Y. Mutations of p16 and p15 tumor suppressor genes and replication errors contribute independently to the pathogenesis of sporadic malignant melanoma. Arch Dermatol Res 1998; 290(4): 175–80.

    Gregory JH, David B. p15INK4B is a potential effector of TGF-?- induced cell cycle arrest. Nature 1994; 371(6494): 258-60.

    Frank H, Raymond B. Loss of the p16ink4a And p15ink4b genes, as well as neighboring 9p21 markers, in sporadic melanoma. Cancer Res 1996; 56(21): 5023-32.

    Yamaguchi Y, Hearing VJ. Melanocyte distribution and function in human skin-effects of ultraviolet radiation. In: Hearing VJ, Leong SPL, editors. From melanocyte to melanoma: The progression to malignancy. Humana Press: New Jersey; 2006: p 101-12.

    Ma SA, O’Day CP, Dentchev T, Takeshita J, Ridky TW, Seykora JT et al. Expression of p15 in a spectrum of spitzoid melanocytic neoplasms. J Cutan Pathol 2019; 46(5): 310-16.

    Shaghaghian E, Namazi MR, Shaghaghian A. Epidemiological Study of Cutaneous Malignant Melanoma in Shiraz, Southwest of Iran between 2011 and 2016; Journal of Molecular Biology Research 2019; 9(1): 106-110.

    Ohsie SJ, Horst BA, Cochran A, Binder SW. Tissue-based protein biomarkers in melanoma: Immunohistochemistry. In: Murphy MJ editor. Diagnostic and prognostic biomarkers and therapeutic targets in melanoma. 1th ed. USA: Springer; 2012. p 159-62.

    Bilinski C, LaChance A, Murphy MJ. Clinical and histopathological parameters in melanoma. In: Murphy MJ (ed). Diagnostic and prognostic biomarkers and therapeutic targets in melanoma.1ed. USA: Springer; 2012. p49-63.

    Ramirez RA, Segovia CG, Rodriquez VG, Baez PG, Flores MG, Candiani JO. Dermoscopic features of acral melanocytic nevi in a series from Mexico. An Bras Dermatol 2018; 93(5): 665-70.

    Malagoli C, Malavolti M, Farnetani F, Longo C, Filippini T, Pellacani G et al. Food and beverage consumption and melanoma risk: A population –Based Case-Control Study in Northern Italy. Nutrients 2019; 11(2206): 1-19.

    Enninga EA, Moser JC, Weaver AL, Markovic SN, Brewer JD, Leontovich AA et al. Survival of cutaneous melanoma based on sex, age and stage in the United States, 1992-2011. Cancer Medicine 2017; 6(10): 2203-12.

    Mikoshiba Y, Minagawa A, Koga H, Yokokawa Y, Uhara H, Okuyama R. Clinical and histopathologic characteristics of melanocytic lesions on the volar skin without typical dermoscopic patterns. Jamadermatology 2019; 13: 2-7.

    Li QX, Swanson DL, Tu P, Yang SX, Li H. Clinical and dermoscopic features of surgically treated melanocytic nevi: a retrospective study of 1046 cases. Chinese Medical Journal 2019; 132(17): 2027-32.

    Ozgur E, Karakullukcu B, Eskiizmir G. Current treatment strategies in cutaneous malignant melanoma of the head and neck. ENT Updates 2019; 9(1): 25-33.

    Seebode C, Lehmann J, Emmert S. Photocarcinogenesis and skin cancer prevention strategis. Anticancer Res 2016; 36(3): 1371-8.

    Davis, LE, Shalin SC, Tackett AJ. Current state of melanoma diagnosis and treatment. Cancer Biology and Therapy 2019; 20(11): 1366-79.

    Tod BM, Schneider JW, Bowcock AM, Kotze MJ. The tumor genetics of acral melanoma: What should a dermatologist know. JAAD Int 2020;1(2):135-47.

    Merkel EA, Gerami P. Malignant melanoma of sun-protected sites: a review of clinical, histological and molecular features. Laboratory investigation 2017; 00: 1-5

    Mufti ST, Falemban A, Rizwan Z. Clinicopathological features of melanocytic nevi and their correlation to cutaneous melanoma among patiens attending King Abdul Aziz University Hospital, Jeddah, Saudi Arabia. Sudan J Med Sci. 2018;13(2):98-113.

    Lotz M, Budden T, Furney SJ, Viros A. Molecular subtype, biological sex and age shape melanoma tumour evolution. BJD 2020; 1-9

    Joshi K, Atwal D, Ravilla R, Pandey Y, Yarlagadda N, Kakadia S et al. Immunotherapy outcomes in advanced melanoma in relation to age. Perm J 2020; 24(19): 1-5.

    Guy GP, Thomas CC, Thompson T, Watson M, Massetti GM, Richardson LC. Vital Signs: Melanoma Incidence and Mortality Trends and Projections — United States, 1982–2030. MMWR 2015; 64(21);591-96.




    DOI: https://doi.org/10.32539/JKK.V8I3.12582

    Refbacks

    • There are currently no refbacks.


    ISSN (Print) : 2406-7431
    E-ISSN (Online) : 2614-0411
     
    Editorial Office
    Fakultas Kedokteran Universitas Sriwijaya
    Jl. Dr. Moehammad Ali Kompleks RSMH Palembang 30126, Indonesia
    Telp. 0711-352342, Fax.: 0711-373438
    email: jurnalfkunsri@gmail.com

     
    Creative Commons License
    Jurnal Kedokteran dan Kesehatan : Publikasi Ilmiah Fakultas Kedokteran Universitas Sriwijaya by https://ejournal.unsri.ac.id/index.php/jkk is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.