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心脏糖苷作为潜在药物的出现:癌症治疗的当前和未来范围。

Emergence of Cardiac Glycosides as Potential Drugs: Current and Future Scope for Cancer Therapeutics.

机构信息

Department of Genomic Science, School of Biological Sciences, Central University of Kerala, Tejaswini Hills, Periya (P.O) Kasaragod, Kerala 671320, India.

Department of Biotechnology, Manonmaniam Sundaranar University, Tirunelveli, Tamilnadu 627012, India.

出版信息

Biomolecules. 2021 Aug 25;11(9):1275. doi: 10.3390/biom11091275.


DOI:10.3390/biom11091275
PMID:34572488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8465509/
Abstract

Cardiac glycosides are natural sterols and constitute a group of secondary metabolites isolated from plants and animals. These cardiotonic agents are well recognized and accepted in the treatment of various cardiac diseases as they can increase the rate of cardiac contractions by acting on the cellular sodium potassium ATPase pump. However, a growing number of recent efforts were focused on exploring the antitumor and antiviral potential of these compounds. Several reports suggest their antitumor properties and hence, today cardiac glycosides (CG) represent the most diversified naturally derived compounds strongly recommended for the treatment of various cancers. Mutated or dysregulated transcription factors have also gained prominence as potential therapeutic targets that can be selectively targeted. Thus, we have explored the recent advances in CGs mediated cancer scope and have considered various signaling pathways, molecular aberration, transcription factors (TFs), and oncogenic genes to highlight potential therapeutic targets in cancer management.

摘要

强心苷是天然甾体化合物,是从植物和动物中分离出来的一组次级代谢产物。这些强心药物在治疗各种心脏疾病方面得到了广泛认可和接受,因为它们可以通过作用于细胞钠钾 ATP 酶泵来增加心脏收缩率。然而,最近越来越多的努力集中在探索这些化合物的抗肿瘤和抗病毒潜力上。有几项报告表明它们具有抗肿瘤特性,因此,如今强心苷(CG)代表了治疗各种癌症的最具多样性的天然衍生化合物,强烈推荐使用。突变或失调的转录因子也作为潜在的治疗靶点而备受关注,可以进行选择性靶向治疗。因此,我们探讨了 CG 介导的癌症范围的最新进展,并考虑了各种信号通路、分子异常、转录因子(TFs)和致癌基因,以突出癌症管理中的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/250ce52259ed/biomolecules-11-01275-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/0f49bda321bc/biomolecules-11-01275-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/24fe1493f83b/biomolecules-11-01275-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/d8563b82440e/biomolecules-11-01275-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/250ce52259ed/biomolecules-11-01275-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/0f49bda321bc/biomolecules-11-01275-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/24fe1493f83b/biomolecules-11-01275-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/d8563b82440e/biomolecules-11-01275-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/8465509/250ce52259ed/biomolecules-11-01275-g004.jpg

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本文引用的文献

[1]
Cardiac Glycoside Ouabain Exerts Anticancer Activity Downregulation of STAT3.

Front Oncol. 2021-6-30

[2]
Cardiac Glycosides as Immune System Modulators.

Biomolecules. 2021-4-29

[3]
Anticancer potential of cardiac glycosides and steroid-azole hybrids.

Steroids. 2021-7

[4]
Artificial intelligence, machine learning, and drug repurposing in cancer.

Expert Opin Drug Discov. 2021-9

[5]
Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.

CA Cancer J Clin. 2021-5

[6]
Cytotoxicity of glucoevatromonoside alone and in combination with chemotherapy drugs and their effects on Na,K-ATPase and ion channels on lung cancer cells.

Mol Cell Biochem. 2021-4

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Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy.

Mol Cancer. 2021-1-15

[8]
MYC as a Multifaceted Regulator of Tumor Microenvironment Leading to Metastasis.

Int J Mol Sci. 2020-10-18

[9]
Cardiac glycosides inhibit cancer through Na/K-ATPase-dependent cell death induction.

Biochem Pharmacol. 2020-12

[10]
Transcription Factors in Cancer Development and Therapy.

Cancers (Basel). 2020-8-15

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