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犬乳腺肿瘤患者 PALB2 基因 WD40 结构域的遗传分析。

Genetic analysis of PALB2 gene WD40 domain in canine mammary tumour patients.

机构信息

Department of Genetics, Faculty of Veterinary Medicine, Kafkas University, Kars, Türkiye.

Department of Genetics, Faculty of Veterinary Medicine, Ankara University, Ankara, Türkiye.

出版信息

Vet Med Sci. 2024 May;10(3):e1366. doi: 10.1002/vms3.1366.

Abstract

BACKGROUND

DNA repair mechanisms are essential for tumorigenesis and disruption of HR mechanism is an important predisposing factor of human breast cancers (BC). PALB2 is an important part of the HR. There are similarities between canine mammary tumours (CMT) and BCs. As its human counterpart, PALB2 mutations could be a predisposing factor of CMT.

OBJECTIVES

In this study, we aimed to investigate the impacts of PALB2 variants on tumorigenesis and canine mammary tumor (CMT) malignancy.

METHODS

We performed Sanger sequencing to detect germline mutations in the WD40 domain of the canine PALB2 gene in CMT patients. We conducted in silico analysis to investigate the variants, and compared the germline PALB2 mutations in humans that cause breast cancer (BC) with the variants detected in dogs with CMT.

RESULTS

We identified an intronic (c.3096+8C>G) variant, two exonic (p.A1050V and p.R1354R) variants, and a 3' UTR variant (c.4071T>C). Of these, p.R1354R and c.4071T>C novel variants were identified for the first time in this study. We found that the p.A1050V mutation had a significant effect. However, we could not determine sufficient similarity due to the differences in nucleotide/amino acid sequences between two species. Nonetheless, possible variants of human sequences in the exact location as their dog counterparts are associated with several cancer types, implying that the variants could be crucial for tumorigenesis in dogs. Our results did not show any effect of the variants on tumor malignancy.

CONCLUSIONS

The current project is the first study investigating the relationship between the PALB2 gene WD40 domain and CMTs. Our findings will contribute to a better understanding of the pathogenic mechanism of the PALB2 gene in CMTs. In humans, variant positions in canines have been linked to cancer-related phenotypes such as familial BC, endometrial tumor, and hereditary cancer predisposition syndrome. The results of bioinformatics analyses should be investigated through functional tests or case-control studies.

摘要

背景

DNA 修复机制对于肿瘤发生至关重要,而 HR 机制的破坏是人类乳腺癌(BC)的一个重要诱发因素。PALB2 是 HR 的重要组成部分。犬乳腺肿瘤(CMT)与 BC 有相似之处。与人类相对应,PALB2 突变可能是 CMT 的一个诱发因素。

目的

本研究旨在探讨 PALB2 变异对肿瘤发生和犬乳腺肿瘤(CMT)恶性程度的影响。

方法

我们对 CMT 患者的 PALB2 基因 WD40 结构域的种系突变进行了 Sanger 测序。我们进行了计算机分析来研究这些变异,并比较了导致人类乳腺癌(BC)的 PALB2 基因突变与在患有 CMT 的犬中检测到的变异。

结果

我们鉴定出一个内含子(c.3096+8C>G)变异、两个外显子(p.A1050V 和 p.R1354R)变异和一个 3'UTR 变异(c.4071T>C)。其中,p.R1354R 和 c.4071T>C 是本研究首次发现的新变异。我们发现 p.A1050V 突变具有显著影响。然而,由于两个物种核苷酸/氨基酸序列的差异,我们无法确定足够的相似性。尽管如此,与人类序列在确切位置的可能变异与几种癌症类型相关,这表明这些变异可能对犬的肿瘤发生至关重要。我们的研究结果并未显示这些变异对肿瘤恶性程度的影响。

结论

本研究首次探讨了 PALB2 基因 WD40 结构域与 CMT 之间的关系。我们的研究结果将有助于更好地理解 PALB2 基因在 CMT 中的致病机制。在人类中,犬种中的变异位置与癌症相关表型相关,如家族性 BC、子宫内膜肿瘤和遗传性癌症易感性综合征。应该通过功能测试或病例对照研究来研究生物信息学分析的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/617c/10962921/3c62ab2a9725/VMS3-10-e1366-g002.jpg

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