在基于生物信息学分析的结直肠癌中识别自和血管生成调节剂
Fariba Shakeri1, Parisa Mohamadynejad1, Mehdi Moghanibashi2
1Department of Biology, Faculty of Basic Sciences, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.
Nucleosides, nucleotides & nucleic acids
|October 4, 2023
概括
这项研究确定ADIPOQ和SLC7A5是结直肠癌 (CRC) 进展中的关键分子参与者. ADIPOQ的下调和SLC7A5的上调与CRC患者的存活率较差有关.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 生物信息学是一种生物信息学.
背景情况:
- 结肠直肠癌 (CRC) 是全球癌症死亡的主要原因.
- 识别新的分子通路和预后生物标志物对于CRC管理至关重要.
研究的目的:
- 发现新的分子途径和结直肠癌的潜在预后生物标志物.
- 分析基因表达数据,以更深入地了解CRC病原性.
主要方法:
- 获取并分析了五个基因表达综合 (GEO) 微阵列数据集.
- 使用癌症基因组图谱 (TCGA) 数据库验证了差异表达的基因.
- 构建了竞争的内源RNA (ceRNA) 网络,并进行了途径分析.
主要成果:
- 在CRC中鉴定出185个差异表达的基因 (17 lncRNA,30 miRNA,138 mRNA)
- 在CRC中,ceRNA网络涉及到ADIPOQ (下调) 和SLC7A5 (上调).
- ADIPOQ和SLC7A5分别参与AMPK和mTOR信号传递,并且与CRC患者的整体存活率相关.
结论:
- ADIPOQ的下调和SLC7A5的上调有助于CRC的进展.
- 这些分子变化与mTORC1活性增加,自减少和血管生成增强有关.
- ADIPOQ和SLC7A5作为结直肠癌的潜在预后生物标志物.
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