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男性乳腺癌:多基因检测在意大利患者队列中的应用结果

Male Breast Cancer: Results of the Application of Multigene Panel Testing to an Italian Cohort of Patients.

作者信息

Tedaldi Gianluca, Tebaldi Michela, Zampiga Valentina, Cangini Ilaria, Pirini Francesca, Ferracci Elisa, Danesi Rita, Arcangeli Valentina, Ravegnani Mila, Martinelli Giovanni, Falcini Fabio, Ulivi Paola, Calistri Daniele

机构信息

Biosciences Laboratory, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, 47014 Meldola, Italy.

Biostatistics and Clinical Trials Unit, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, 47014 Meldola, Italy.

出版信息

Diagnostics (Basel). 2020 Apr 30;10(5):269. doi: 10.3390/diagnostics10050269.

Abstract

Male breast cancer (MBC) is a rare tumor, accounting for less than 1% of all breast cancers. In MBC, genetic predisposition plays an important role; however, only a few studies have investigated in depth the role of genes other than and . We performed a Next-Generation Sequencing (NGS) analysis with a panel of 94 cancer predisposition genes on germline DNA from an Italian case series of 70 patients with MBC. Moreover, we searched for large deletions/duplications of genes through the Multiplex Ligation-dependent Probe Amplification (MLPA) technique. Through the combination of NGS and MLPA, we identified three pathogenic variants in the gene and six in the gene. Besides these alterations, we found six additional pathogenic/likely-pathogenic variants in , , , , and genes. From our study, and emerge as the main genes associated with MBC risk, but also other genes seem to be associated with the disease. Indeed, some of these genes have already been implicated in female breast cancer predisposition, but others are known to be involved in other types of cancer. Consequently, our results suggest that novel genes could be involved in MBC susceptibility, shedding new light on their role in cancer development.

摘要

男性乳腺癌(MBC)是一种罕见肿瘤,占所有乳腺癌的比例不到1%。在男性乳腺癌中,遗传易感性起着重要作用;然而,只有少数研究深入调查了除[基因名称1]和[基因名称2]之外的其他基因的作用。我们对来自意大利70例男性乳腺癌患者病例系列的种系DNA进行了下一代测序(NGS)分析,检测了一组94个癌症易感基因。此外,我们通过多重连接依赖探针扩增(MLPA)技术搜索了[相关基因名称]的大片段缺失/重复。通过将NGS和MLPA相结合,我们在[基因名称1]基因中鉴定出三个致病变异,在[基因名称2]基因中鉴定出六个致病变异。除了这些改变,我们还在[基因名称3]、[基因名称4]、[基因名称5]、[基因名称6]和[基因名称7]基因中发现了另外六个致病/可能致病的变异。从我们的研究中可以看出,[基因名称1]和[基因名称2]是与男性乳腺癌风险相关的主要基因,但其他一些基因似乎也与该疾病有关。事实上,其中一些基因已经被认为与女性乳腺癌易感性有关,但其他一些基因已知与其他类型的癌症有关。因此,我们的结果表明,新的基因可能参与男性乳腺癌的易感性,为它们在癌症发展中的作用提供了新的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3680/7277207/19d1cb5e996f/diagnostics-10-00269-g001.jpg

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