吩噻嗪衍生物及其对细胞凋亡过程的影响

IF 2.8 4区 医学 Q3 TOXICOLOGY
Michał Otręba, Łukasz Marek, Piotr Paduszyński, Jerzy Stojko, Anna Rzepecka-Stojko
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引用次数: 0

摘要

几十年来,吩噻嗪衍生物作为抗精神病药物用于多种精神健康和身体状况的治疗(精神分裂症、双相情感障碍中的躁狂症和精神病)。流行病学研究表明,精神分裂症患者患癌症的可能性较小,这表明抗精神病药物能够抑制癌细胞的发展。这是我们第三次回顾吩噻嗪衍生物对细胞死亡的影响。这里,我们关注的是细胞凋亡。我们选择了92篇研究吩噻嗪衍生物对正常细胞和癌细胞凋亡过程影响的论文。氯丙嗪、氟那嗪、左旋丙嗪、哌嗪、正非那嗪、丙嗪、异丙嗪、噻嗪、三氟拉嗪和三氟拉嗪类似物(3dc)更常诱导癌细胞系、人肝细胞和淋巴细胞凋亡,最终效果取决于所用药物的类型和浓度、细胞系的类型和使用的方法。所获得的结果可以更好地理解吩噻嗪衍生物的生物作用,并将有助于将这类药物重新定位于癌症治疗,从而实现更快、更安全、更容易和更便宜的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phenothiazine Derivatives and Their Impact on the Apoptosis Processes: A Review.

Phenothiazine derivatives have been used for decades as antipsychotic drugs in multiple mental health and physical conditions treatment (schizophrenia, mania in bipolar disorder, and psychosis). Epidemiological studies have shown that people with schizophrenia are less likely to suffer from cancer, which indicates the ability of antipsychotics to inhibit the development of cancer cells. It is our third review about the impact of phenothiazine derivatives on cell death. Here, we focused on apoptosis. We selected 92 papers that investigated the effect of phenothiazine derivatives on the apoptosis process in normal and cancer cell lines. Chlorpromazine, fluphenazine, levomepromazine, mepazine, perphenazine, promazine, promethazine, thioridazine, trifluoperazine, and trifluoperazine analog (3dc) more often induce apoptosis in cancer cell lines, human hepatocytes, and lymphocytes, and the final effect depends on the type and concentration of drug used, the type of cell line, and the methodology used. The obtained results allow for a better understanding of the biological action of phenothiazine derivatives and will help reposition this group of drugs to cancer treatment, resulting in faster, safer, easier, and cheaper therapy.

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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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