Study of FABP's interactome and detecting new molecular targets in clear cell renal cell carcinoma

相互作用体 肾细胞癌 细胞 计算生物学 生物 肾透明细胞癌 癌症研究 医学 肿瘤科 遗传学 基因
作者
Guangzhen Wu,Zhiwei Zhang,Qizhen Tang,Lei Liu,Wei Liu,Quanlin Li,Qifei Wang
出处
期刊:Journal of Cellular Physiology [Wiley]
卷期号:235 (4): 3776-3789 被引量:18
标识
DOI:10.1002/jcp.29272
摘要

Fatty acids (FAs) play a crucial role in the development of clear cell renal cell carcinoma (ccRCC), FAs function requires the participation of fatty-acid-binding protein (FABP). Current studies have shown that different members of the FABP's family play different roles in the tumorigenesis of ccRCC. Therefore, the systematic analysis of FABPs will be of great significance. However, the diverse expression patterns and prognostic values of nine FABPs have yet to be elucidated. In this study, through multiple analysis and verification of multiple databases, such as ONCOMINE, The Human Protein Atlas, UALCAN, Gene Expression Profiling Interactive Analysis, and cBioPortal, we found that the expression of FABP1 was significantly downregulated and the expression of FABP5/6/7 was significantly upregulated in ccRCC compared with renal tissues, and the patients with high messenger RNA (mRNA) levels of the FABP5/6/7 or low mRNA levels of FABP1 were predicted to have a lower overall survival or disease-free survival. Further analysis by the protein-protein interaction (PPI), Gene Ontology pathway, and Kyoto Encyclopedia of Genes and Genomes pathway showed that FABPs were mainly involved in the peroxisome proliferator-activated receptor (PPAR) pathway. In coexpression analysis, we found that FABP1/5/6/7 was coexpressed with transforming growth factor-β1 (TGF-β1), PPARA, and LPL. This study implied that FABP1/5/6/7 could act as an important tumor biomarker of ccRCC; the role of FABPs may be related to PPAR or TGF-β pathway.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
ding应助Ballyhooed采纳,获得10
1秒前
嘚嘚发布了新的文献求助10
1秒前
kun完成签到,获得积分10
2秒前
科研通AI6.4应助Facbiu采纳,获得10
2秒前
桐桐应助barrychow采纳,获得10
2秒前
2秒前
3秒前
静谧的薯条完成签到,获得积分10
3秒前
lll完成签到,获得积分10
4秒前
领导范儿应助等待书桃采纳,获得10
5秒前
LUX完成签到,获得积分10
6秒前
单纯飞柏完成签到,获得积分20
6秒前
可爱的函函应助Chen采纳,获得10
7秒前
7秒前
细腻谷南完成签到,获得积分10
8秒前
深情山晴发布了新的文献求助10
8秒前
中南海完成签到,获得积分10
8秒前
9秒前
9秒前
10秒前
科研通AI6.2应助秋心采纳,获得10
10秒前
从笙完成签到,获得积分10
11秒前
11秒前
12秒前
可爱的函函应助惜灵采纳,获得10
12秒前
逍遥游发布了新的文献求助10
12秒前
13秒前
13秒前
14秒前
NexusExplorer应助三里采纳,获得10
14秒前
WW完成签到,获得积分10
15秒前
15秒前
明尘完成签到,获得积分10
15秒前
马路牙子发布了新的文献求助10
16秒前
稻草人发布了新的文献求助10
16秒前
缓慢天抒发布了新的文献求助10
16秒前
寂寞的海发布了新的文献求助10
17秒前
科研通AI6.4应助jinling采纳,获得10
17秒前
Ting发布了新的文献求助10
19秒前
20秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
基于锂离子电池正极材料回收的绿色溶剂开发及工程化应用研究 500
Auslegungsgeschichte 500
Transdermal drug delivery systems market size report 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7642408
求助须知:如何正确求助?哪些是违规求助? 9215419
关于积分的说明 19768587
捐赠科研通 7207644
什么是DOI,文献DOI怎么找? 3276367
关于科研通互助平台的介绍 2438115
邀请新用户注册赠送积分活动 2274102