BAP1型
黑色素瘤
ARID1A型
SMARCA4型
脑转移
基因
转移
医学
癌症研究
突变
生物
肿瘤科
癌症
内科学
遗传学
染色质重塑
表观遗传学
作者
Renáta Váraljai,Susanne Horn,Antje Sucker,Daniela Piercianek,Verena Schmitt,Alexander Carpinteiro,Katrin Anne Becker,J. Reifenberger,Alexander Roesch,Jörg Felsberg,Guido Reifenberger,Ulrich Sure,Dirk Schadendorf,Iris Helfrich
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2021-02-10
卷期号:13 (4): 731-731
被引量:19
标识
DOI:10.3390/cancers13040731
摘要
Background: Development of brain metastases in advanced melanoma patients is a frequent event that limits patients’ quality of life and survival. Despite recent insights into melanoma genetics, systematic analyses of genetic alterations in melanoma brain metastasis formation are lacking. Moreover, whether brain metastases harbor distinct genetic alterations beyond those observed at different anatomic sites of the same patient remains unknown. Experimental Design and Results: In our study, 54 intracranial and 18 corresponding extracranial melanoma metastases were analyzed for mutations using targeted next generation sequencing of 29 recurrently mutated driver genes in melanoma. In 11 of 16 paired samples, we detected nucleotide modifications in brain metastases that were absent in matched metastases at extracranial sites. Moreover, we identified novel genetic variants in ARID1A, ARID2, SMARCA4 and BAP1, genes that have not been linked to brain metastases before; albeit most frequent mutations were found in ARID1A, ARID2 and BRAF. Conclusion: Our data provide new insights into the genetic landscape of intracranial melanoma metastases supporting a branched evolution model of metastasis formation.
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