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犬传染性性病肿瘤中MYC基因的不同DNA甲基化模式和基因表达

Divergent DNA methylation patterns and gene expression in MYC and in canine transmissible venereal tumors.

作者信息

Keopaseuth Soukkangna, Pringproa Kidsadagon, Patchanee Prapas, Setthawongsin Chanokchon, Techangamsuwan Somporn, Chuammitri Phongsakorn

机构信息

Graduate Program in Veterinary Medicine, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai, 50100 Thailand.

Veterinary Bioscience Unit, Veterinary Academic Office, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai, 50100 Thailand.

出版信息

Vet World. 2024 Jul;17(7):1581-1590. doi: 10.14202/vetworld.2024.1581-1590. Epub 2024 Jul 24.

Abstract

BACKGROUND AND AIM

Canine transmissible venereal tumor (CTVT), a unique transmissible cancer in dogs, affects the external genitalia and potentially spreads to other parts of the body. While somatic mutations in oncogenic and tumor-suppressing genes are linked to CTVT development, the impact of DNA methylation, which affects gene expression, remains unclear. This study explored whether DNA methylation in the promoter regions of the MYC oncogene and tumor suppressor genes in CTVTs is associated with their expression, both at the gene and protein levels.

MATERIALS AND METHODS

To investigate promoter DNA methylation of MYC and in CTVTs, we analyzed frozen tissue samples from genital CTVT (GTVTs) and extragenital CTVT (ETVTs). Genomic DNA was extracted, bisulfite-treated, and analyzed using bisulfite polymerase chain reaction (PCR) and sequencing. The messenger RNA and protein of MYC and were also extracted and assessed by real-time PCR and Western blotting. Matching formalin-fixed, paraffin-embedded blocks were used for immunohistochemical staining to visualize protein distribution in GTVT and ETVT tissues.

RESULTS

Although both GTVT and ETVT samples showed MYC promoter methylation, the extent of methylation differed significantly. GTVTs displayed a much higher degree of methylation, potentially explaining the more pronounced downregulation of MYC gene expression and reduction in c-MYC protein levels observed in GTVTs compared with ETVTs. Our data revealed a prevalent hypermethylation pattern in the promoter across both sample types. However, DNA methylation, which was expected to have a suppressive effect, did not correlate with gene/protein expression. GTVTs displayed high protein levels despite significantly reduced expression. Conversely, ETVTs maintained regular expression but exhibited reduced protein production, suggesting a complex interplay between methylation and expression in these tumors.

CONCLUSION

MYC demonstrated a clear association between its promoter methylation status, gene expression, and protein levels; however, lacked this correlation, implying the involvement of methylation-independent regulatory mechanisms and highlighting the need for further investigation.

摘要

背景与目的

犬传染性性病肿瘤(CTVT)是犬类一种独特的传染性癌症,影响外生殖器,并有可能扩散至身体其他部位。虽然致癌基因和抑癌基因的体细胞突变与CTVT的发生发展有关,但影响基因表达的DNA甲基化的作用仍不清楚。本研究探讨了CTVT中MYC癌基因和抑癌基因启动子区域的DNA甲基化是否与其在基因和蛋白质水平的表达相关。

材料与方法

为研究CTVT中MYC和的启动子DNA甲基化情况,我们分析了来自生殖器CTVT(GTVT)和生殖器外CTVT(ETVT)的冷冻组织样本。提取基因组DNA,进行亚硫酸氢盐处理,并使用亚硫酸氢盐聚合酶链反应(PCR)和测序进行分析。还提取了MYC和的信使RNA和蛋白质,并通过实时PCR和蛋白质印迹法进行评估。使用匹配的福尔马林固定、石蜡包埋块进行免疫组织化学染色,以观察GTVT和ETVT组织中蛋白质的分布。

结果

虽然GTVT和ETVT样本均显示MYC启动子甲基化,但甲基化程度差异显著。GTVT显示出更高程度的甲基化,这可能解释了与ETVT相比,GTVT中观察到的MYC基因表达更明显下调和c-MYC蛋白水平降低的原因。我们的数据显示,两种样本类型的启动子中均存在普遍的高甲基化模式。然而,预期具有抑制作用的DNA甲基化与基因/蛋白质表达无关。尽管表达显著降低,但GTVT仍显示出高蛋白水平。相反,ETVT维持正常表达,但蛋白质产生减少,表明这些肿瘤中甲基化与表达之间存在复杂的相互作用。

结论

MYC在其启动子甲基化状态、基因表达和蛋白质水平之间表现出明显的关联;然而,缺乏这种相关性,这意味着存在甲基化非依赖性调节机制,并突出了进一步研究的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e95/11344115/dd929388be7f/Vetworld-17-1581-g001.jpg

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