Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, P.O. Box: 16635-148, Tehran, Iran.
School of Biomedical Engineering, University of Technology Sydney, Sydney, Australia.
Sci Rep. 2021 Jul 23;11(1):15112. doi: 10.1038/s41598-021-94678-4.
Carcinoma of Unknown Primary (CUP) is a heterogeneous and metastatic disease where the primary site of origin is undetectable. Currently, chemotherapy is the only state-of-art treatment option for CUP patients. The molecular profiling of the tumour, particularly mutation detection, offers a new treatment approach for CUP in a personalized fashion using targeted agents. We analyzed the mutation and copy number alterations profile of 1709 CUP samples deposited in the AACR Project Genomics Evidence Neoplasia Information Exchange (GENIE) cohort and explored potentially druggable mutations. We identified 52 significant mutated genes (SMGs) among CUP samples, in which 13 (25%) of SMGs were potentially targetable with either drugs are approved for the know primary tumour or undergoing clinical trials. The most variants detected were TP53 (43%), KRAS (19.90%), KMT2D (12.60%), and CDKN2A (10.30%). Additionally, using pan-cancer analysis, we found similar variants of TERT promoter in CUP and NSCLC samples, suggesting that these mutations may serve as a diagnostic marker for identifying the primary tumour in CUP. Taken together, the mutation profiling analysis of the CUP tumours may open a new way of identifying druggable targets and consequently administrating appropriate treatment in a personalized manner.
不明原发癌(CUP)是一种异质性和转移性疾病,其原发灶无法检测到。目前,化疗是 CUP 患者唯一的标准治疗选择。肿瘤的分子分析,特别是突变检测,为 CUP 患者提供了一种新的个性化治疗方法,使用靶向药物。我们分析了 1709 个 CUP 样本的突变和拷贝数改变图谱,这些样本存储在 AACR 项目基因组证据肿瘤信息交换(GENIE)队列中,并探索了潜在的可用药突变。我们在 CUP 样本中确定了 52 个显著突变基因(SMGs),其中 13 个(25%)SMGs 可以使用已批准用于已知原发性肿瘤或正在进行临床试验的药物进行靶向治疗。检测到的最多变体是 TP53(43%)、KRAS(19.90%)、KMT2D(12.60%)和 CDKN2A(10.30%)。此外,通过泛癌分析,我们在 CUP 和 NSCLC 样本中发现了 TERT 启动子的相似变体,这表明这些突变可能作为识别 CUP 中原发性肿瘤的诊断标志物。总之,CUP 肿瘤的突变分析可能为确定可用药靶标开辟新途径,并随后以个性化方式进行适当治疗。