克雷布斯循环酶基因富马酸氢化酶的种系突变导致两年内四次原发性恶性肿瘤。

Case Reports in Genetics Pub Date : 2024-06-06 eCollection Date: 2024-01-01 DOI:10.1155/2024/5591237
Solaleh Aminian, Fawaz Al-Alloosh, Fatemeh Yadegari, Shiva Zarinfam, Haider Hamza Al-Abedi, Keivan Majidzadeh-A
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引用次数: 0

摘要

多发性原发性癌症(MPCs)是指一个人身上出现一种以上的癌症,但不是因为复发、转移或局部扩散。共同致病基因突变、环境因素、生活方式和首次癌症治疗等不同因素会增加后续恶性肿瘤发生的可能性。近年来,由于治疗方法的改进,发生多发性肺癌的风险有所增加;然而,四重原发性恶性肿瘤仍然罕见,需要进一步调查和治疗其根本原因。在此,我们介绍了一名有 40 年吸烟史的 64 岁男性,他患上了会厌、肾、胰腺和肺的四重原发性恶性肿瘤。为了研究可能的遗传原因,我们进行了 WES 检测,结果在克雷布斯循环酶基因富马酸氢化酶(FH)的第 5 号外显子中发现了一个 c.580G > A (Ala194Thr) 的变异。该变异在 Clinvar 中被归类为 VUS,在 Varsome 和 Franklin 软件中被归类为可能致病。结构分析表明,发现的变异位于富马酸水合酶铰链区附近的 D2 结构域中高度保守的 alpha 螺旋上(见图 2)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quadruple Primary Malignancies over 2 Years with Germline Mutation in Krebs Cycle Enzyme Gene Fumarate Hydratase.

Multiple primary cancers (MPCs) are defined as the presence of more than one cancer in an individual that is not due to recurrence, metastasis, or local spread. Different factors such as copathogenic genetic mutations, environmental factors, lifestyle, and first cancer treatment increase the possible occurrence of subsequent malignancies. In recent years, the risk of MPCs has increased due to improved treatment; however, quadruple primary malignancies are still rare and require further investigation and treatment of the underlying cause. Here, we present a 64-year-old man with a 40-year history of cigarette smoking who developed quadruple primary malignancies of the epiglottis, kidney, pancreas, and lung. To investigate the possible genetic cause, we performed WES, and a variant of c.580G > A (Ala194Thr) was discovered in exon 5 of the Krebs cycle enzyme gene, fumarate hydratase (FH). This substitution was classified as VUS in Clinvar and likely pathogenic by Varsome and Franklin software. The structural analysis showed that the variation found was localized in a highly conserved alpha helix in the D2 domain near the FH hinge region (<6 Å), suggesting that enzyme activity was affected by a perturbation in protein quaternary structure. Because of the well-established role of FH mutations in renal cancer risk, it was possible that the FH mutation could have led to the development of renal cell carcinoma in this case. The biological mechanisms of MPCs suggest that subsequent primary malignancies are triggered by the combined effects of environmental factors, such as smoking and genetics.

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