TIMM8B在卵巢癌中通过抑制mtROS/ASK1/JNK信号通路促进氧化磷酸化和糖酵解。

IF 4.9 2区 生物学 Q1 BIOLOGY
Yue Jia, Jiaqian Liao, Xiangqun Yang, Hongyan Hu, Wentao Zhao, Liufang Zhao, Conghui Ai, Yuanbo Xue, Shufen Tan, Yi Zhang
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引用次数: 0

摘要

背景:卵巢癌是一种复杂的异质性疾病。在本研究中,我们研究了在卵巢癌中差异表达的基因TIMM8B的功能意义,以更好地了解该疾病发展的分子过程。方法:对卵巢癌组织及癌旁非癌组织进行RNA测序。从测序数据(转录本)、TCGA-OV和GSE14407中获得的mRNA表达谱随后被用于鉴定共同的deg。对这些常见deg进行GO、KEGG通路和PPI网络分析。检测TIMM8B在卵巢癌组织和细胞系中的表达。TIMM8B对细胞行为的影响,如增殖、凋亡、迁移、侵袭和能量代谢,通过基于细胞的实验来评估。此外,我们还研究了TIMM8B通过mtROS/ASK1/JNK信号通路对这些过程的调控。结果:在卵巢癌中共鉴定出233个常见deg。氧化石墨烯分析结果显示细胞外基质组织、含胶原的细胞外基质和跨膜转运蛋白活性等富集。KEGG通路分析结果显示,deg参与氧化磷酸化和糖酵解/糖异生等通路。TIMM8B在卵巢癌组织和细胞系中表达上调。TIMM8B增强卵巢癌细胞的氧化磷酸化、糖酵解、增殖、迁移和侵袭,并抑制凋亡。TIMM8B通过抑制mtROS/ASK1/JNK信号通路发挥作用。结论:TIMM8B可能调控mtROS/ASK1/JNK通路,导致氧化磷酸化和糖酵解增加。靶向TIMM8B及其相关信号通路可能有助于开发新的卵巢癌治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TIMM8B promotes oxidative phosphorylation and glycolysis by inhibiting the mtROS/ASK1/JNK signaling pathway in ovarian cancer.

Background: Ovarian cancer is a complicated and heterogeneous disease. In this study, we investigated the functional significance of the gene TIMM8B, which is differentially expressed in ovarian cancer to better understand the molecular processes involved in the development of this disease.

Methods: RNA sequencing was performed on ovarian cancer tissues and adjacent noncancerous tissues. The mRNA expression profiles obtained from the sequencing data (transcripts), TCGA-OV, and GSE14407 were subsequently used to identify common DEGs. GO, KEGG pathway, and PPI network analyses of these common DEGs were conducted. The expression of TIMM8B was examined in ovarian cancer tissues and cell lines. The effects of TIMM8B on cellular behaviors, such as proliferation, apoptosis, migration, invasion, and energy metabolism, were assessed by conducting cell-based assays. Additionally, the regulation of these processes by TIMM8B through the mtROS/ASK1/JNK signaling pathway was investigated.

Results: A total of 233 common DEGs were identified in ovarian cancer. The results of the GO analysis revealed enrichment in extracellular matrix organization, collagen-containing extracellular matrix, and transmembrane transporter activity, among others. The results of the KEGG pathway analysis revealed the involvement of DEGs in pathways such as oxidative phosphorylation and glycolysis/gluconeogenesis. TIMM8B was upregulated in ovarian cancer tissues and cell lines. TIMM8B enhanced oxidative phosphorylation, glycolysis, proliferation, migration, and invasion and inhibited apoptosis in ovarian cancer cells. TIMM8B was found to exert its effects through the suppression of mtROS/ASK1/JNK signaling.

Conclusion: TIMM8B may regulate the mtROS/ASK1/JNK pathways, leading to an increase in oxidative phosphorylation and glycolysis. Targeting TIMM8B and its associated signaling pathway may help in the development of new treatment approaches for ovarian cancer.

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来源期刊
Biology Direct
Biology Direct 生物-生物学
CiteScore
6.40
自引率
10.90%
发文量
32
审稿时长
7 months
期刊介绍: Biology Direct serves the life science research community as an open access, peer-reviewed online journal, providing authors and readers with an alternative to the traditional model of peer review. Biology Direct considers original research articles, hypotheses, comments, discovery notes and reviews in subject areas currently identified as those most conducive to the open review approach, primarily those with a significant non-experimental component.
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