Literature DB >> 20713185

Preferential killing of cancer cells with mitochondrial dysfunction by natural compounds.

Gang Chen1, Feng Wang, Dunyaporn Trachootham, Peng Huang.   

Abstract

Mitochondria play essential roles in cellular metabolism, redox homeostasis, and regulation of cell death. Emerging evidences suggest that cancer cells exhibit various degrees of mitochondrial dysfunctions and metabolic alterations, which may serve as a basis to develop therapeutic strategies to preferentially kill the malignant cells. Mitochondria as a therapeutic target for cancer treatment is gaining much attention in the recent years, and agents that impact mitochondria with anticancer activity have been identified and tested in vitro and in vivo using various experimental systems. Anticancer agents that directly target mitochondria or indirectly affect mitochondrial functions are collectively classified as mitocans. This review article focuses on several natural compounds that preferentially kill cancer cells with mitochondrial dysfunction, and discusses the possible underlying mechanisms and their therapeutic implications in cancer treatment. Mitocans that have been comprehensively reviewed recently are not included in this article. Important issues such as therapeutic selectivity and the relevant biochemical basis are discussed in the context of future perspectives. Published by Elsevier B.V.

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Year:  2010        PMID: 20713185      PMCID: PMC3085019          DOI: 10.1016/j.mito.2010.08.001

Source DB:  PubMed          Journal:  Mitochondrion        ISSN: 1567-7249            Impact factor:   4.160


  197 in total

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Review 3.  Metabolic control analysis indicates a change of strategy in the treatment of cancer.

Authors:  Rafael Moreno-Sánchez; Emma Saavedra; Sara Rodríguez-Enríquez; Juan Carlos Gallardo-Pérez; Héctor Quezada; Hans V Westerhoff
Journal:  Mitochondrion       Date:  2010-06-25       Impact factor: 4.160

4.  Evidence of ROS generation by mitochondria in cells with impaired electron transport chain and mitochondrial DNA damage.

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Journal:  Mitochondrion       Date:  2006-12-13       Impact factor: 4.160

5.  NADPH oxidase 1 plays a critical mediating role in oncogenic Ras-induced vascular endothelial growth factor expression.

Authors:  D Komatsu; M Kato; J Nakayama; S Miyagawa; T Kamata
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6.  Sodium pancratistatin 3,4-o-cyclic phosphate, a water-soluble synthetic derivative of pancratistatin, is highly effective in a human colon tumor model.

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7.  Honokiol induces cell apoptosis in human chondrosarcoma cells through mitochondrial dysfunction and endoplasmic reticulum stress.

Authors:  Ying-Ju Chen; Chien-Lin Wu; Ju-Fang Liu; Yi-Chin Fong; Sheng-Feng Hsu; Te-Mao Li; Yi-Chang Su; Shing-Hwa Liu; Chih-Hsin Tang
Journal:  Cancer Lett       Date:  2009-10-31       Impact factor: 8.679

8.  Rapid reactive oxygen species (ROS) generation induced by curcumin leads to caspase-dependent and -independent apoptosis in L929 cells.

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9.  Menadione-induced DNA damage in a human tumor cell line.

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Journal:  Blood       Date:  2006-09-07       Impact factor: 22.113

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  25 in total

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2.  A novel synthetic C-1 analogue of 7-deoxypancratistatin induces apoptosis in p53 positive and negative human colorectal cancer cells by targeting the mitochondria: enhancement of activity by tamoxifen.

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Review 3.  From serendipity to mitochondria-targeted nanocarriers.

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4.  Simple discrimination of sub-cycling cells by propidium iodide flow cytometric assay in Jurkat cell samples with extensive DNA fragmentation.

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Journal:  Cell Cycle       Date:  2018-04-10       Impact factor: 4.534

5.  Differentially expressed genes and microRNAs in bladder carcinoma cell line 5637 and T24 detected by RNA sequencing.

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Journal:  Int J Clin Exp Pathol       Date:  2015-10-01

Review 6.  Targeting cancer cell mitochondria as a therapeutic approach.

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Journal:  Future Med Chem       Date:  2013-01       Impact factor: 3.808

7.  Mitochondrial dysfunction induced by honokiol.

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8.  Preferential killing of human lung cancer cell lines with mitochondrial dysfunction by nonthermal dielectric barrier discharge plasma.

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9.  Iodinin (1,6-dihydroxyphenazine 5,10-dioxide) from Streptosporangium sp. induces apoptosis selectively in myeloid leukemia cell lines and patient cells.

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10.  Shikonin directly targets mitochondria and causes mitochondrial dysfunction in cancer cells.

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