Department of Internal Medicine, Vali-e-Asr Hospital, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.
Zanjan Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran.
Asian Pac J Cancer Prev. 2024 May 1;25(5):1547-1558. doi: 10.31557/APJCP.2024.25.5.1547.
Several recent studies suggest that chromodomain-helicase -DNA-binding domains (CHDs) are linked with cancers. We explored the association between chromodomain-Helicase-DNA-binding domain proteins and breast cancer (BrCa) and introduced potential prognostic markers using various databases.
We analyzed the expression of the CHD family and their prognostic value in BrCa by mining UALCAN, TIMER, and Kaplan-Meier plotter databases. The association of CHD expression and immune infiltrating abundance was studied via the TIMER database. In addition, microRNAs related to the CHD family were identified by using the MirTarBase online database.
The present study indicated that compared to normal tissues, BrCa tissues showed increased mRNA levels of CHD3/4/7 but decreased CHD2/5/9 expression. Interestingly, We also found a positive correlation between CHD gene expression and the infiltration of macrophage, neutrophil, and dendritic cells in BrCa, except CHD3/5. The Kaplan-Meier Plotter analysis suggested that high expression levels of CHD1/2/3/4/6/8/9 were significantly related to shorter relapse-free survival (RFS), while higher mRNA expression of CHD1, CHD2, CHD8, and CHD9 was significantly associated with longer overall survival of BrCa patients. The miRNAs of hsa-miR-615-3p and hsa-let-7b-5p were identified as being more correlated with the CHD family.
The altered expression of some CHD members was significantly related to clinical cancer outcomes, and CHD1/2/8/9 could serve as potential prognostic biomarkers to improve the survival of BrCa patients. However, to evaluate the studied CHD members in detail are needed further investigations including experimental validation.
最近的几项研究表明,染色质结构域-解旋酶-DNA 结合域(CHDs)与癌症有关。我们通过各种数据库探讨了 CHD 蛋白与乳腺癌(BrCa)的相关性,并引入了潜在的预后标志物。
我们通过挖掘 UALCAN、TIMER 和 Kaplan-Meier plotter 数据库,分析了 CHD 家族在 BrCa 中的表达及其预后价值。通过 TIMER 数据库研究了 CHD 表达与免疫浸润丰度的相关性。此外,还使用 MirTarBase 在线数据库鉴定了与 CHD 家族相关的 microRNA。
本研究表明,与正常组织相比,BrCa 组织中 CHD3/4/7 的 mRNA 水平升高,而 CHD2/5/9 的表达降低。有趣的是,我们还发现 CHD 基因表达与 BrCa 中巨噬细胞、中性粒细胞和树突状细胞浸润呈正相关,除 CHD3/5 外。Kaplan-Meier Plotter 分析表明,CHD1/2/3/4/6/8/9 的高表达水平与较短的无复发生存(RFS)显著相关,而 CHD1、CHD2、CHD8 和 CHD9 的高 mRNA 表达与 BrCa 患者的总生存时间延长显著相关。hsa-miR-615-3p 和 hsa-let-7b-5p 的 miRNA 被鉴定为与 CHD 家族更相关。
一些 CHD 成员的改变表达与临床癌症结局显著相关,CHD1/2/8/9 可以作为潜在的预后生物标志物,改善 BrCa 患者的生存。然而,需要进一步的研究,包括实验验证,以详细评估所研究的 CHD 成员。