Clinical applications of (epi)genetics in gastroenteropancreatic neuroendocrine neoplasms: Moving towards liquid biopsies

被引:12
|
作者
Boons, Gitta [1 ,2 ,3 ,4 ]
Vandamme, Timon [1 ,2 ,3 ,4 ,5 ]
Peeters, Marc [1 ,2 ]
Van Camp, Guy [1 ,2 ,3 ,4 ]
Op de Beeck, Ken [1 ,2 ,3 ,4 ]
机构
[1] Univ Antwerp, Ctr Oncol Res CORE, Univ Pl 1, B-2610 Antwerp, Belgium
[2] Antwerp Univ Hosp, Univ Pl 1, B-2610 Antwerp, Belgium
[3] Univ Antwerp, Ctr Med Genet, Prins Boudewijnlaan 43, B-2650 Edegem, Belgium
[4] Antwerp Univ Hosp, Prins Boudewijnlaan 43, B-2650 Edegem, Belgium
[5] Erasmus MC, Div Endocrinol, Dept Internal Med, Dr Molewaterpl 50, NL-3015 GE Rotterdam, Netherlands
来源
关键词
Gastroenteropancreatic Neuroendocrine Neoplasms; Genetics; Epigenetics; Biomarkers; Liquid Biopsies; PANCREATIC ENDOCRINE TUMORS; CELL LINES BON-1; YIN-YANG; CARCINOID-TUMORS; DNA METHYLATION; MICRORNA EXPRESSION; CLINICOPATHOLOGICAL FEATURES; MOLECULAR CHARACTERISTICS; EPIGENETIC DYSREGULATION; PROGNOSTIC RELEVANCE;
D O I
10.1007/s11154-019-09508-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
High-throughput analysis, including next-generation sequencing and microarrays, have strongly improved our understanding of cancer biology. However, genomic data on rare cancer types, such as neuroendocrine neoplasms, has been lagging behind. Neuroendocrine neoplasms (NENs) develop from endocrine cells spread throughout the body and are highly heterogeneous in biological behavior. In this challenging disease, there is an urgent need for new therapies and new diagnostic, prognostic, follow-up and predictive biomarkers to aid patient management. The last decade, molecular data on neuroendocrine neoplasms of the gastrointestinal tract and pancreas, termed gastroenteropancreatic NENs (GEP-NENs), has strongly expanded. The aim of this review is to give an overview of the recent advances on (epi)genetic level and highlight their clinical applications to address the current needs in GEP-NENs. We illustrate how molecular alterations can be and are being used as therapeutic targets, how mutations in DAXX/ATRX and copy number variations could be used as prognostic biomarkers, how far we are in identifying predictive biomarkers and how genetics can contribute to GEP-NEN classification. Finally, we discuss recent studies on liquid biopsies in the field of GEP-NENs and illustrate how liquid biopsies can play a role in patient management. In conclusion, molecular studies have suggested multiple potential biomarkers, but further validation is ongoing.
引用
收藏
页码:333 / 351
页数:19
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