Pan-cancer analysis and experimental validation revealed the m6A methyltransferase KIAA1429 as a potential biomarker for diagnosis, prognosis, and immunotherapy

被引:0
|
作者
Ma, Chao [1 ,2 ]
Zheng, Qiming [3 ]
Wang, Yepeng [1 ]
Li, Guoxiang [1 ]
Zhao, Mengmeng [4 ]
Sun, Zhigang [1 ]
机构
[1] Shandong First Med Univ, Cent Hosp, Dept Thorac Surg, Jinan 250013, Shandong, Peoples R China
[2] Weifang Med Univ, Sch Clin Med, Weifang 261053, Shandong, Peoples R China
[3] Shandong Univ, Jinan Cent Hosp, Jinan 250013, Shandong, Peoples R China
[4] Shandong First Med Univ, Cent Hosp, Res Ctr Translat Med, Jinan 250013, Shandong, Peoples R China
来源
AGING-US | 2023年 / 15卷 / 17期
基金
中国博士后科学基金;
关键词
KIAA1429; pan-cancer; diagnosis; prognosis; immune infiltration; RNA METHYLATION;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: KIAA1429, also known as VIRMA (vir-like m6A methyltransferase associated), plays a crucial role in tumorigenesis by modulating the level of m6A methylation. Previous studies have reported the prevalent overexpression of KIAA1429 in multiple cancers, related to a poor prognosis. Nevertheless, the precise role of KIAA1429 in tumor progression and its impact on the immune response remains unclear. Methods: A differential analysis of KIAA1429 expression was performed across cancers using data from the Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) databases. We evaluated the role of KIAA1429 in the diagnosis, prognosis, and immunotherapy of tumor patients using bioinformatics methods. In addition, we also analyzed the associations between KIAA1429 and DNA methylation, immunotherapy. RT-qPCR was used to study the expression levels of KIAA1429 mRNA in 11 cell lines. Results: KIAA1429 is found to be overexpressed in 28 cancer types, but its expression is relatively low in patients with acute myeloid leukemia (LAML) and ovarian serous cystadenocarcinoma (OV). Moreover, KIAA1429 demonstrates a positive correlation with advanced stages of multiple cancers. Kaplan-Meier (KM) analysis suggested that patients with elevated KIAA1429 expression had shorter survival. Furthermore, KIAA1429 shows strong associations with DNA methylation, tumor-infiltrating immune cells (TIICs), and the tumor microenvironment (TME). RT-qPCR results indicated significantly higher expression of KIAA1429 in tumor cells compared to matched-normal cells. Conclusions: In summary, our work illustrates that KIAA1429 expression is positively connected with poor prognosis in multiple cancers. Moreover, KIAA1429 could serve as a diagnostic factor and a predictor of immune response for specific tumor types.
引用
收藏
页码:8664 / 8691
页数:28
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