Suppr超能文献

胃癌细胞中 EB 病毒和幽门螺杆菌共感染的激酶状态。

Status of kinases in Epstein-Barr virus and Helicobacter pylori Coinfection in gastric Cancer cells.

机构信息

The Discipline of Biosciences and Biomedical Engineering, Indian Institute of Technology Indore, Room no. 302, School Building, IIT Indore, Khandwa Road, Simrol, Indore, 453552, India.

Choithram Hospital and Research Centre Indore, Indore, Madhya Pradesh, India.

出版信息

BMC Cancer. 2020 Sep 29;20(1):925. doi: 10.1186/s12885-020-07377-0.

Abstract

BACKGROUND

Helicobacter pylori (H. pylori) and Epstein - Barr virus (EBV) plays a significant role in aggressive gastric cancer (GC). The investigation of genes associated with these pathogens and host kinases may be essential to understand the early and dynamic progression of GC.

AIM

The study aimed to demonstrate the coinfection of EBV and H. pylori in the AGS cells through morphological changes, expression of the kinase and the probable apoptotic pathways.

METHODS

Genomic DNA isolation of H. pylori and its characterization from clinical samples were performed. RT-qPCR of kinases was applied to scrutinize the gene expression of kinases in co-infected GC in a direct and indirect (separated through insert size 0.45 μm) H. pylori infection set up. Morphological changes in co-infected GC were quantified by measuring the tapering ends of gastric epithelial cells. Gene expression profiling of apoptotic genes was assessed through RT-qPCR.

RESULTS

An interleukin-2-inducible T-cell kinase (ITK) showed significant upregulation with indirect H. pylori infection. Moreover, Ephrin type-B receptor six precursors (EPHB6) and Tyrosine-protein kinase Fyn (FYN) showed significant upregulation with direct coinfection. The tapering ends in AGS cells were found to be extended after 12 h. A total of 24 kinase genes were selected, out of which EPHB6, ITK, FYN, and TYK2 showed high expression as early as 12 h. These kinases may lead to rapid morphological changes in co-infected gastric cells. Likewise, apoptotic gene expression such as APAF-1 and Bcl2 family genes such as BAD, BID, BIK, BIM, BAX, AND BAK were significantly down-regulated in co-infected AGS cells.

CONCLUSION

All the experiments were performed with novel isolates of H. pylori isolated from central India, for the functional assessment of GC. The effect of coinfection with EBV was more profoundly observed on morphological changes in AGS cells at 12 h as quantified by measuring the tapering of ends. This study also identifies the kinase and apoptotic genes modulated in co-infected cells, through direct and indirect approaches. We report that ITK, EPHB6, TYK2, FYN kinase are enhanced, whereas apoptotic genes such as APAF-1, BIK, FASL, BAX are significantly down-regulated in AGS cells coinfected with EBV and H. pylori.

摘要

背景

幽门螺杆菌(H. pylori)和 Epstein-Barr 病毒(EBV)在侵袭性胃癌(GC)中发挥重要作用。研究与这些病原体和宿主激酶相关的基因可能对于理解 GC 的早期和动态进展至关重要。

目的

本研究旨在通过形态变化、激酶表达和可能的凋亡途径,证明 EBV 和 H. pylori 在 AGS 细胞中的共感染。

方法

从临床样本中分离 H. pylori 并对其进行基因组 DNA 分离。应用 RT-qPCR 检测共感染 GC 中激酶的基因表达,直接和间接(通过插入大小 0.45 μm 分离)H. pylori 感染设置。通过测量胃上皮细胞的变细端来量化共感染 GC 中的形态变化。通过 RT-qPCR 评估凋亡基因的表达谱。

结果

白细胞介素 2 诱导的 T 细胞激酶(ITK)在间接 H. pylori 感染时表现出显著上调。此外,Ephrin 型-B 受体六前体(EPHB6)和酪氨酸蛋白激酶 Fyn(FYN)在直接共感染时表现出显著上调。AGS 细胞的变细端在 12 小时后被发现延长。总共选择了 24 个激酶基因,其中 EPHB6、ITK、FYN 和 TYK2 在 12 小时时表现出高表达。这些激酶可能导致共感染胃细胞的快速形态变化。同样,共感染 AGS 细胞中的凋亡基因表达如 APAF-1 和 Bcl2 家族基因如 BAD、BID、BIK、BIM、BAX 和 BAK 显著下调。

结论

所有实验均使用从印度中部分离的新型 H. pylori 进行,用于 GC 的功能评估。在 12 小时时通过测量变细端,更深入地观察到 EBV 共感染对 AGS 细胞形态变化的影响。这项研究还通过直接和间接方法鉴定了共感染细胞中调节的激酶和凋亡基因。我们报告说,ITK、EPHB6、TYK2 和 FYN 激酶增强,而凋亡基因如 APAF-1、BIK、FASL 和 BAX 在 EBV 和 H. pylori 共感染的 AGS 细胞中显著下调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a5a/7523314/f488e43c6d2e/12885_2020_7377_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验