多环芳香碳化合物通过调节烯碳化合物受体来调节鼻癌的发生和发展
Zhicong Hong1,2,3, Qiaoling Guo1,2,3, Xianyang Luo1,2,3
1Department of Otolaryngology-Head and Neck Surgery, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University.
The Tohoku journal of experimental medicine
|September 11, 2024
概括
发现多环芳化合物 (PAHs) 抑制了亡并增加了鼻癌 (NPC) 细胞中的酸受体 (AhR) 表达. 这些发现表明,PAHs通过调节AhR,有助于NPC的发展.
科学领域:
- 在瘤学瘤学.
- 环境健康 环境健康
- 分子生物学分子生物学
背景情况:
- 鼻癌 (NPC) 呈现为晚期诊断和转移,病因不明.
- 多环芳 (PAH),环境污染物,是致变种和致癌的,但它们在NPC中的作用需要进一步研究.
研究的目的:
- 研究PAHs对NPC细胞行为的影响和烯碳化合物受体 (AhR) 的表达.
- 阐明AhR在PAH诱导的NPC细胞变化中的作用.
主要方法:
- CNE-2 NPC细胞被暴露在PAHs中.
- 使用qRT-PCR和西布洛特分析了AhR和CYP1A2的基因和蛋白质表达.
- 细胞增殖,迁移,入侵和细胞亡被评估使用CCK-8,伤口愈合试验,Transwell和流动细胞计.
主要成果:
- PAHs增加了NPC细胞中的AhR表达,并抑制了apoptosis.
- 氧化并没有显著改变NPC细胞的增殖或迁移,但削弱了入侵.
- 与PAH和ITE的同时治疗抵消了PAH诱导的AhR上调和亡的增加.
结论:
- PAHs抑制了亡,并在鼻癌细胞中促进了AhR的表达.
- 通过AhR调节,PAHs似乎会影响NPC的发生和进展.
- 针对AhR可能为NPC提供潜在的治疗策略.
相关概念视频
Transducer Mechanism: Nuclear Receptors
1.3K
Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, development, or metabolism. Their ability to be stimulated by small lipophilic ligands and control vital cellular processes makes them ideal drug targets. Nearly 10-15% of currently prescribed drugs target these receptors.
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
1.3K
Cancer Prevention
6.1K
Several factors can increase the risk of cancer in an individual. About 50% of cancer cases can be prevented by adopting a healthy lifestyle, regular exercise, eating healthy, and following a modest cancer prevention diet. Epidemiological studies have consistently shown that populations with vegetable and fruit-rich diets have reduced the incidence of cancer. On the other hand, populations who have a diet rich in animal fat, red meat, junk food, or high calories are predisposed to cancer.
Some...
Some...
6.1K
Mutagenicity and Carcinogenicity
1.2K
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
1.2K
Abnormal Proliferation
4.5K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.5K
GPCRs Regulate Adenylyl Cylase Activity
5.3K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.3K
Nucleophilic Aromatic Substitution: Elimination–Addition
4.0K
Simple aryl halides do not react with nucleophiles. However, nucleophilic aromatic substitutions can be forced under certain conditions, such as high temperatures or strong bases. The mechanism of substitution under such conditions involves the highly unstable and reactive benzyne intermediate. Benzyne contains equivalent carbon centers at both ends of the triple bond, each of which is equally susceptible to nucleophilic attack. This 50–50 distribution of products is...
4.0K


