OGG1 contributes to hepatocellular carcinoma by promoting cell cycle-related protein expression and enhancing DNA oxidative damage repair in tumor cells.
OGG1 contributes to hepatocellular carcinoma by promoting cell cycle-related protein expression and enhancing DNA oxidative damage repair in tumor cells.
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OGG1通过促进细胞周期相关蛋白表达并增强肿瘤细胞中DNA氧化损伤修复来促进肝细胞癌
DOI:
10.1002/jcla.24561
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发表时间:
2022-07
影响因子:
2.7
通讯作者:
Chen, Jie
中科院分区:
文献类型:
--
作者:
Zhang, He;Jiang, Peng-jun;Lv, Meng-yuan;Zhao, Yan-hua;Cui, Ju;Chen, Jie
This study aimed to analyze the expression of 8‐oxoguanine DNA glycosylase (OGG1) in patients with hepatocellular carcinoma (HCC) and its effect on prognosis by bioinformatics techniques and to determine its possible carcinogenic mechanism through data mining. The difference in OGG1 expression between healthy people and HCC patients was searched and analyzed by TCGA and GEO databases, and the effect of OGG1 on prognosis was judged by survival analysis. Meanwhile, the possible molecular mechanism of OGG1 in the tumorigenesis and development of HCC was explored by GO analysis, KEGG analysis, immune infiltration analysis, protein–protein interaction network, promoter methylation analysis, and so forth. Quantitative polymerase chain reaction (qPCR) was used to examine the gene expression in 36 pairs of HCC tissues and adjacent tissues. The expression of OGG1 in HCC patients was higher than that in healthy people, and the overexpression of OGG1 might stimulate cell proliferation by increasing the activity of cell cycle‐related proteins. The alteration of OGG1 was significantly correlated with the tumorigenesis and development of HCC. OGG1 is expected to be a new biomarker for evaluating the prognosis of HCC and a new target for the treatment of HCC. Figure 1 Expression of OGG1 in HCC, (A) expression of OGG1 in nucleoplasma, (B, C) OGG1 expression in healthy liver tissues, (D, E, F) OGG1 expression in liver tissues of HCC patients (G) expression of OGG1 in HCC based on sample type (H) nodal metastasis status (I) TP53 mutation status (J) age (K) gender (L) race (M) stage (N) grade (O) histological subtype.
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影响因子:
2.9
作者:
Guan Q;Chen Z;Chen Q;Zhi X
通讯作者:
Zhi X
影响因子:
2
作者:
Sakata, Kazuhito;Yoshizumi, Tomoharu;Mori, Masaki
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Mori, Masaki
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5.6
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Hanna BMF;Michel M;Helleday T;Mortusewicz O
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Mortusewicz O
影响因子:
3.7
作者:
van de Klundert MA;van Hemert FJ;Zaaijer HL;Kootstra NA
通讯作者:
Kootstra NA
影响因子:
5.7
作者:
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