疾病领域 | 数量 |
---|---|
感染 | 1 |
排名前五的药物类型 | 数量 |
---|---|
预防性疫苗 | 1 |
排名前五的靶点 | 数量 |
---|---|
SARS-CoV-2 antigen(新冠病毒抗原) | 1 |
作用机制 新冠病毒抗原抑制剂 |
在研适应症 |
非在研适应症- |
最高研发阶段临床3期 |
首次获批国家/地区- |
首次获批日期- |
靶点- |
作用机制- |
在研机构- |
在研适应症- |
非在研适应症 |
最高研发阶段无进展 |
首次获批国家/地区- |
首次获批日期- |
开始日期2024-10-25 |
申办/合作机构 |
开始日期2024-09-15 |
申办/合作机构 Selcuk University [+1] |
开始日期2024-01-01 |
申办/合作机构 |
Malignant pleural mesothelioma (MPM) is a rare type of cancer, and its main risk factor is exposure to asbestos. Accordingly, our knowledge of the genomic structure of an MPM tumor is limited when compared to other cancers. In this study, we aimed to characterize complex genomic rearrangement patterns and variations to better understand the genomics of MPM tumors. We comparatively scanned 3 MPM tumor genomes by Whole-Genome Sequencing and High-Resolution SNP array. We also used various computational algorithms to detect both CNAs and complex chromosomal rearrangements. Genomic data obtained from each bioinformatics tool are interpreted comparatively to better understand CNAs and cancer-related Nucleotide variations in MPM tumors. In patients 1 and 2, we found pathogenic nucleotide variants of <i>BAP1, RB1,</i> and <i>TP53</i>. These two MPM genomes exhibited a highly rearranged chromosomal rearrangement pattern resembling Chromomanagesis particularly in the form of Chromoanasynthesis. In patient 3, we found nucleotide variants of important cancer-related genes, including <i>TGFBR1, KMT2C,</i> and <i>PALLD</i>, to have lower chromosomal rearrangement complexity compared with patients 1 and 2. We also detected several actionable nucleotide variants including XR<i>CC1, ERCC2</i>. We also discovered the <i>SKA3-DDX10</i> fusion in two MPM genomes, which is a novel finding for MPM. We found that MPM genomes are very complex, suggesting that this highly rearranged pattern is strongly related to driver mutational status like <i>BAP1, TP53</i> and <i>RB1</i>.