Actionable Mutation Profile of Sun-Protected Melanomas in South America
Nenhuma Miniatura disponível
Citações na Scopus
0
Tipo de produção
article
Data de publicação
2022
Título da Revista
ISSN da Revista
Título do Volume
Editora
LIPPINCOTT WILLIAMS & WILKINS
Autores
CAMILLO, Claudia M. C.
OLIVEIRA, Katia K.
CARRARO, Dirce M.
SANGUEZA, Martin
Citação
AMERICAN JOURNAL OF DERMATOPATHOLOGY, v.44, n.10, p.741-747, 2022
Resumo
Melanomas that arise in sun-protected sites, including acral and oral mucosal melanomas, are likely under the control of unique, specific mechanisms that lead to mutagenesis through various pathways. In this study, we examined somatic mutations in tumors by targeted sequencing using a custom Ion Ampliseq Panel, comprising hotspots of 14 genes that are frequently mutated in solid tumors. Tumor DNA was extracted from 9 formalin fixation, paraffin-embedded sun-protected melanomas (4 primary oral mucosal melanomas and 5 acral lentiginous melanomas), and we identified mutations in the NRAS, PIK3CA, EGFR, HRAS, ERBB2, and ROSI genes. This study reveals new actionable mutations that are potential targets in the treatment of photo-protected melanomas. Additional studies on more of these melanoma subtypes could confirm our findings and identify new mutations.
Palavras-chave
acral lentiginous melanoma, primary oral mucosal melanoma, mutation, sun-protected, next-generation sequencing
Referências
- Aguas SC, 2009, MED ORAL PATOL ORAL, V14, pE265
- Akslen LA, 2008, MELANOMA RES, V18, P29, DOI 10.1097/CMR.0b013e3282f32517
- [Anonymous], 2020, COSMIC CATALOGUE SOM
- Berra CM, 2019, APPL CANC RES, V39, P1, DOI 10.1186/s41241-019-0075-2
- Boone B, 2011, J CUTAN PATHOL, V38, P492, DOI 10.1111/j.1600-0560.2011.01673.x
- Borkowska Aneta, 2020, Oncotarget, V11, P2404, DOI 10.18632/oncotarget.27642
- Bustos BD, 2017, SCI REP-UK, V7, DOI 10.1038/s41598-017-00606-w
- Couts KL, 2018, MOL CANCER THER, V17, P222, DOI 10.1158/1535-7163.MCT-17-0472
- Davies KD, 2013, CLIN CANCER RES, V19, P4040, DOI 10.1158/1078-0432.CCR-12-2851
- de Biase D, 2020, DIAGNOSTICS, V10, DOI 10.3390/diagnostics10040250
- Desai A, 2017, CLIN EXP DERMATOL, V42, P845, DOI 10.1111/ced.13243
- Dietel M, 2015, CANCER GENE THER, V22, P417, DOI 10.1038/cgt.2015.39
- Dika E, 2020, AM J CLIN PATHOL, V153, P664, DOI 10.1093/ajcp/aqz209
- El-Deeb IM, 2011, MED RES REV, V31, P794, DOI 10.1002/med.20206
- Garzino-Demo P, 2004, J CRANIO MAXILL SURG, V32, P251, DOI 10.1016/j.jcms.2003.12.007
- Goswami RS, 2015, CLIN CANCER RES, V21, P2644, DOI 10.1158/1078-0432.CCR-14-2391
- Gottesdiener LS, 2018, CLIN CANCER RES, V24, P5815, DOI 10.1158/1078-0432.CCR-18-1397
- Haugh AM, 2018, J INVEST DERMATOL, V138, P384, DOI 10.1016/j.jid.2017.08.022
- Hsieh R, 2017, AM J DERMATOPATH, V39, P104, DOI 10.1097/DAD.0000000000000605
- Hsieh R, 2013, AM J DERMATOPATH, V35, P167, DOI 10.1097/DAD.0b013e31825fa1f6
- Janku F, 2011, PLOS ONE, V6, DOI 10.1371/journal.pone.0022769
- Kosmidou V, 2014, HUM MUTAT, V35, P329, DOI 10.1002/humu.22496
- Kuchelmeister C, 2000, BRIT J DERMATOL, V143, P275, DOI 10.1046/j.1365-2133.2000.03651.x
- Lee SH, 2016, CANCER RES TREAT, V48, P853, DOI 10.4143/crt.2014.356
- Lourenco SV, 2009, AM J DERMATOPATH, V31, P323, DOI 10.1097/DAD.0b013e3181a0d37c
- Lv JJ, 2016, SCI REP-UK, V6, DOI 10.1038/srep31432
- Manca A, 2015, J TRANSL MED, V13, DOI 10.1186/s12967-015-0401-8
- Merkel EA, 2017, LAB INVEST, V97, P630, DOI 10.1038/labinvest.2016.147
- Mikkelsen LH, 2016, APMIS, V124, P475, DOI 10.1111/apm.12529
- Nogueira C, 2010, ONCOGENE, V29, P6222, DOI 10.1038/onc.2010.349
- Olbryt M, 2020, TARGET ONCOL, V15, P101, DOI 10.1007/s11523-020-00695-0
- Omholt K, 2006, MELANOMA RES, V16, P197, DOI 10.1097/01.cmr.0000200488.77970.e3
- Rakosy Z, 2007, INT J CANCER, V121, P1729, DOI 10.1002/ijc.22928
- Schaefer T, 2017, MEDICINE, V96, DOI 10.1097/MD.0000000000005753
- Serrati S, 2016, ONCOTARGETS THER, V9, P7355, DOI 10.2147/OTT.S99807
- Shayanfar Nasrin, 2015, Asian Pac J Cancer Prev, V16, P421
- Shi Katherine, 2019, J Am Acad Dermatol, DOI 10.1016/j.jaad.2019.07.017
- Shim JH, 2017, EXP DERMATOL, V26, P883, DOI 10.1111/exd.13321
- Silva JM, 2017, PIGM CELL MELANOMA R, V30, P353, DOI 10.1111/pcmr.12586
- Sini MC, 2018, ONCOTARGET, V9, P8531, DOI 10.18632/ONCOTARGET.23989
- Sortino-Rachou AM, 2009, ORAL ONCOL, V45, P254, DOI 10.1016/j.oraloncology.2008.04.015
- Tamirat MZ, 2020, J VIS EXP, V2020, P1
- Thomas NE, 2015, JAMA ONCOL, V1, P359, DOI 10.1001/jamaoncol.2015.0493
- Turner J, 2017, PIGM CELL MELANOMA R, V30, P53, DOI 10.1111/pcmr.12560
- Uguen A, 2016, FUTURE ONCOL, V12, P1911, DOI 10.2217/fon-2016-0050
- Ulivieri Alessandra, 2015, Oncotarget, V6, P19868
- Wei XT, 2020, ANN SURG ONCOL, V27, P3478, DOI 10.1245/s10434-020-08418-5
- Whitwam T, 2007, ONCOGENE, V26, P4563, DOI 10.1038/sj.onc.1210239
- Xu YC, 2020, J COMPUT BIOL, V27, P9, DOI 10.1089/cmb.2019.0197
- Zaremba A, 2019, EUR J CANCER, V119, P66, DOI 10.1016/j.ejca.2019.07.008
- Zebary A, 2013, J DERMATOL SCI, V72, P284, DOI 10.1016/j.jdermsci.2013.07.013