Minna Emanuela, Romeo Paola, Dugo Matteo, De Cecco Loris, Aiello Antonella, Pistore Federico, Carenzo Andrea, Greco Angela, Borrello Maria Grazia
Molecular Mechanisms Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.
Department of Medical Oncology, IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
Cancers (Basel). 2022 Apr 13;14(8):1951. doi: 10.3390/cancers14081951.
Medullary thyroid carcinoma (MTC) is a rare but aggressive tumor. Although and genes are recognized drivers in MTC, associated downstream signaling pathways are largely unknown. In this study, we report 17 sporadic MTCs, collected at our institution, comprising patient-matched primary and lymph node metastatic tumors investigated for mutational and transcriptional profiles. As we identified two uncommon deletions (D898_E901del and E632_L633del), we also performed a literature review and meta-analysis to assess the occurrence of unconventional alterations in MTC, focusing on next-generation sequencing studies. We found that new gene alterations are emerging, along with the known drivers, involving not only by multiple concurrent mutations or deletions but also other previously underestimated cancer-related genes, especially in sporadic MTCs. In our MTC gene profiles, we found transcriptome similarity between patient-matched tissues and expression of immune genes only by a few samples. Furthermore, we defined a gene signature able to stratify samples into two distinct signaling types, termed MEN2B-like and MEN2A-like. We provide an updated overview of the MTC mutational spectrum and describe how transcriptional profiles can be used to define distinct MTC signaling subtypes that appear to be shared by various gene drivers, including the unconventional ones.
甲状腺髓样癌(MTC)是一种罕见但侵袭性强的肿瘤。尽管 和 基因被认为是MTC的驱动基因,但其相关的下游信号通路在很大程度上尚不清楚。在本研究中,我们报告了在我们机构收集的17例散发性MTC,包括患者匹配的原发性和淋巴结转移性肿瘤,对其进行了突变和转录谱研究。由于我们鉴定出两个罕见的 缺失(D898_E901del和E632_L633del),我们还进行了文献综述和荟萃分析,以评估MTC中非常规改变的发生率,重点关注下一代测序研究。我们发现,除了已知的 驱动基因外,新的基因改变正在出现,不仅涉及 因多个同时发生的突变或缺失,还涉及其他先前被低估的癌症相关基因,尤其是在散发性MTC中。在我们的MTC基因谱中,我们发现患者匹配组织之间的转录组相似性,并且只有少数样本表达免疫基因。此外,我们定义了一种基因特征,能够将样本分为两种不同的信号类型,称为MEN2B样和MEN2A样。我们提供了MTC突变谱的最新概述,并描述了转录谱如何用于定义不同的MTC信号亚型,这些亚型似乎由各种基因驱动因素共享,包括非常规的驱动因素。