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在患有多发性原发性结直肠癌的结直肠癌家族中寻找种系基因变异。

Search for germline gene variants in colorectal cancer families presenting with multiple primary colorectal cancers.

作者信息

Försti Asta, Ambrozkiewicz Filip, Marciniak Magdalena, Lubinski Jan, Hemminki Kari

机构信息

Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.

Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Heidelberg, Germany.

出版信息

Int J Cancer. 2025 Apr 1;156(7):1393-1403. doi: 10.1002/ijc.35283. Epub 2024 Dec 10.

Abstract

A double primary colorectal cancer (CRC) in a familial setting signals a high risk of CRC. In order to identify novel CRC susceptibility genes, we whole-exome sequenced germline DNA from nine persons with a double primary CRC and a family history of CRC. The detected variants were processed by bioinformatics filtering and prioritization, including STRING protein-protein interaction and pathway analysis. A total of 150 missense, 19 stop-gain, 22 frameshift and 13 canonical splice site variants fulfilled our filtering criteria. The STRING analysis identified 20 DNA repair/cell cycle proteins as the main cluster, related to genes CHEK2, EXO1, FAAP24, FANCI, MCPH1, POLL, PRC1, RECQL, RECQL5, RRM2, SHCBP1, SMC2, XRCC1, in addition to CDK18, ENDOV, ZW10 and the known mismatch repair genes. Another STRING network included extracellular matrix genes and TGFβ signaling genes. In the nine whole-exome sequenced patients, eight harbored at least two candidate DNA repair/cell cycle/TGFβ signaling gene variants. The number of families is too small to provide evidence for individual variants but, considering the known role of DNA repair/cell cycle genes in CRC, the clustering of multiple deleterious variants in the present families suggests that these, perhaps jointly, contributed to CRC development in these families.

摘要

家族性背景下的双原发性结直肠癌(CRC)预示着患CRC的高风险。为了鉴定新的CRC易感基因,我们对9名患有双原发性CRC且有CRC家族史的个体的生殖系DNA进行了全外显子测序。检测到的变异通过生物信息学过滤和优先级排序进行处理,包括STRING蛋白质-蛋白质相互作用和通路分析。共有150个错义变异、19个终止密码子获得变异、22个移码变异和13个经典剪接位点变异符合我们的过滤标准。STRING分析确定20种DNA修复/细胞周期蛋白为主要聚类,这些蛋白与CHEK2、EXO1、FAAP24、FANCI、MCPH1、POLL、PRC1、RECQL、RECQL5、RRM2、SHCBP1、SMC2、XRCC1等基因相关,此外还有CDK18、ENDOV、ZW10以及已知的错配修复基因。另一个STRING网络包括细胞外基质基因和TGFβ信号基因。在9名进行全外显子测序的患者中,8名至少携带两个候选DNA修复/细胞周期/TGFβ信号基因变异。家族数量过少,无法为单个变异提供证据,但是,考虑到DNA修复/细胞周期基因在CRC中的已知作用,本研究中家族中多个有害变异的聚集表明,这些变异可能共同促成了这些家族中CRC的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d0c/11789446/ae34c84f996f/IJC-156-1393-g002.jpg

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