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[I型干扰素在黑色素瘤基因进展中的潜在作用]

[Potential role of type I interferon in the genetic progression of melanoma].

作者信息

Vízkeleti Laura, Ladányi Andrea, Papp Orsolya, Doma Viktória, Kárpáti Sarolta, Rásó Erzsébet, Barbai Tamás, Tímár József

机构信息

Patológiai, Igazságügyi és Biztosítási Orvostani Intézet, Semmelweis Egyetem, Budapest, Hungary.

Sebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Nemzeti Tumorbiológiai Laboratórium, Budapest, Hungary.

出版信息

Magy Onkol. 2023 Sep 28;67(3):215-221. Epub 2023 Aug 18.

Abstract

We have followed the genomic progression of cutaneous melanoma in visceral metastases using genome-wide copy number analysis. We have detected an increased chromosomal instability due to the loss of several DNA repair genes. Furthermore, we found co-amplifications of HGF and MET genes in metastases. The most interesting finding was gene amplifications of several, mostly IFN-regulated immune cell genes in lung metastases. Next we have defined a type I IFN resistance gene expression signature (GES) using human cell lines, several elements of which were proved to be stable in vitro and in vivo as well. The components of this GES have been detected in TCGA as well as in publicly available datasets of immunotherapy-treated melanoma cases. In case of samples from previously IFN-treated melanoma cases we have identified treatment-specific genomic alterations (predominantly amplifications) which were most characteristic for brain metastases.

摘要

我们通过全基因组拷贝数分析追踪了皮肤黑色素瘤内脏转移中的基因组进展。我们检测到由于多个DNA修复基因的缺失导致染色体不稳定性增加。此外,我们在转移灶中发现了HGF和MET基因的共扩增。最有趣的发现是在肺转移灶中几个主要受IFN调节的免疫细胞基因的扩增。接下来,我们利用人类细胞系定义了一种I型干扰素抗性基因表达特征(GES),其中几个元件在体外和体内均被证明是稳定的。这种GES的组成成分在TCGA以及免疫治疗的黑色素瘤病例的公开可用数据集中也被检测到。对于先前接受过IFN治疗的黑色素瘤病例的样本,我们鉴定出了治疗特异性的基因组改变(主要是扩增),这些改变在脑转移中最为典型。

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