Review the Role of Metabolism Reprogramming in the Pathogenesis ofPost-surgical Adhesion: A New Therapeutic Strategy

糖酵解 细胞生物学 重编程 厌氧糖酵解 癌症研究 转化生长因子 PI3K/AKT/mTOR通路 SMAD公司 生物 信号转导 代谢途径 免疫系统 细胞 免疫学 新陈代谢 生物化学
作者
Mohsen Aliakbarian,Rozita Khodashahi,Mahmoud Tavakkoli,Kiarash Ashrafzadeh,Hoda Rahimi,Ebrahim Khaleghi,Majid Ghayour‐Mobarhan,Mohammad‐Hassan Arjmand
出处
期刊:Current Topics in Medicinal Chemistry [Bentham Science]
卷期号:23 (27): 2527-2534 被引量:1
标识
DOI:10.2174/0115680266253222231011102151
摘要

Abstract: Metabolic reprogramming is defined as the skill of cells to change their metabolism to support the induced energy demand due to continuous growth. Metabolic reprogramming is a well- known occurrence in the progression of neoplastic cells, although, evidence has shown that it is present in fibrotic disorders. Post-surgical adhesion as a fibrotic disorder is a medical challenge and is defined by fibrotic bands connected between organs with the abdominal wall. Despite many investigations carried out about the pathogenesis of the disorder but there are many unknowns, therefore, targeting special pathways may have the potential to prevent the formation of fibrotic bands post-operative. Glycolysis is a necessary metabolic pathway in living cells. In hypoxic conditions, it is the dominant pathway in the production of energy for different types of cells such as fibroblasts, immune cells, and endothelial cells. Also, glycolysis is a main downstream target for transforming growth factor β (TGF-β) and upregulates during fibrotic conditions. Furthermore, this is noteworthy that hypoxia induces factor 1 alpha (HIF-1α) as a transcription factor, elevated during the hypoxia condition stimulates different signaling pathways such as TGF-β/SMAD, nuclear factor kappa B (NF-kB), and mTOR pathway to control glycolytic metabolism and T-cell trafficking for immune cell migration. Different evidence has indicated that the administration of glycolytic inhibitors has the potential to prevent the development of fibrotic markers. In this review, we pointed out the role of the glycolysis pathway and its connection to profibrotic cytokines to promote inflammatory and fibrotic pathways. Based on the results of studies related to fibrotic disorders we hypothesized that targeting glycolysis may have therapeutic potential in the prevention of postoperative adhesions.
最长约 10秒,即可获得该文献文件

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
1秒前
老实的鞋垫完成签到,获得积分10
1秒前
慕迎蕾发布了新的文献求助10
1秒前
量子星尘发布了新的文献求助10
1秒前
海海完成签到,获得积分10
2秒前
阳光新筠应助自然小猫咪采纳,获得30
2秒前
Russell发布了新的文献求助10
3秒前
南风完成签到,获得积分10
3秒前
愉快三问发布了新的文献求助10
4秒前
5秒前
崔风机发布了新的文献求助10
7秒前
Russell完成签到,获得积分10
7秒前
9秒前
蜻蜓完成签到,获得积分10
10秒前
10秒前
11秒前
yorxx发布了新的文献求助10
11秒前
852应助优美紫槐采纳,获得10
12秒前
13秒前
kk完成签到,获得积分10
13秒前
FashionBoy应助悦耳的初之采纳,获得10
13秒前
14秒前
李可乐发布了新的文献求助10
14秒前
yangchang完成签到,获得积分20
14秒前
14秒前
14秒前
她在他城发布了新的文献求助10
14秒前
量子星尘发布了新的文献求助10
15秒前
orixero应助机智的访云采纳,获得10
15秒前
量子星尘发布了新的文献求助10
16秒前
大个应助koui采纳,获得10
17秒前
18秒前
18秒前
kk发布了新的文献求助10
19秒前
丢丢第发布了新的文献求助10
20秒前
崔风机完成签到,获得积分20
21秒前
Yezo发布了新的文献求助10
22秒前
Nirvana发布了新的文献求助10
23秒前
eiiinx发布了新的文献求助10
23秒前
脑洞疼应助糟糕的立辉采纳,获得10
23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
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1000
The Composition and Relative Chronology of Dynasties 16 and 17 in Egypt 1000
Russian Foreign Policy: Change and Continuity 800
Real World Research, 5th Edition 800
Qualitative Data Analysis with NVivo By Jenine Beekhuyzen, Pat Bazeley · 2024 800
Superabsorbent Polymers 700
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5712031
求助须知:如何正确求助?哪些是违规求助? 5207432
关于积分的说明 15266074
捐赠科研通 4864074
什么是DOI,文献DOI怎么找? 2611194
邀请新用户注册赠送积分活动 1561461
关于科研通互助平台的介绍 1518793