Center for Oncological Research (CORE), University of Antwerp and Antwerp University Hospital, Universiteitsplein 1, 2610, Wilrijk, Belgium.
Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Prins Boudewijnlaan 43, 2650, Edegem, Belgium.
Rev Endocr Metab Disord. 2019 Sep;20(3):333-351. doi: 10.1007/s11154-019-09508-w.
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.
高通量分析,包括下一代测序和微阵列,大大提高了我们对癌症生物学的理解。然而,包括神经内分泌肿瘤在内的罕见癌症类型的基因组数据却一直滞后。神经内分泌肿瘤(NENs)起源于遍布全身的内分泌细胞,其生物学行为具有高度异质性。在这种具有挑战性的疾病中,迫切需要新的治疗方法和新的诊断、预后、随访和预测性生物标志物来辅助患者管理。在过去的十年中,胃肠道和胰腺神经内分泌肿瘤(称为胃肠胰神经内分泌肿瘤(GEP-NENs))的分子数据已经大大扩展。本文的目的是概述(表观)遗传学水平的最新进展,并强调其在临床中的应用,以满足 GEP-NEN 的当前需求。我们举例说明了分子改变如何以及正在被用作治疗靶点,DAXX/ATRX 突变和拷贝数变异如何可以用作预后生物标志物,我们在确定预测生物标志物方面已经走了多远,以及遗传学如何有助于 GEP-NEN 的分类。最后,我们讨论了 GEP-NEN 领域的液体活检的最新研究,并说明了液体活检如何在患者管理中发挥作用。总之,分子研究已经提出了多种潜在的生物标志物,但仍在进行进一步的验证。