Literature DB >> 20407854

Knockdown of SOD1 sensitizes the CD34+ CML cells to imatinib therapy.

Li Liu1, Renan Chen, Siyong Huang, Yanlan Wu, Guohui Li, Qiang Liu, Dandan Yin, Yingmin Liang.   

Abstract

Leukemia stem cell is thought to be one of the leading causes of imatinib resistance and the resultant relapse of chronic myelogenous leukemia (CML). Eradicating the leukemia stem cells holds the promise of CML treatment. In this study, we found that the CD34+ subpopulation in the CML cell line K562 had a higher expression of SOD1 than that in the CD34 negative cells. Knockdown of SOD1 in CD34+ cells had no significant effects on cell survival and growth, while it sensitized the CD34+ cells to imatinib therapy. N-acetyl-L cysteine (NAC) blocked the pro-apoptotic effects of SOD1 knockdown, suggesting the antioxidant effects of SOD1 was essential for the resistance of CD34+ cells to imatinib therapy. In summary, our results suggest that antagonizing the enhanced endogenous antioxidant activity in leukemia stem cells sheds lights on CML therapy.

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Year:  2010        PMID: 20407854     DOI: 10.1007/s12032-010-9529-9

Source DB:  PubMed          Journal:  Med Oncol        ISSN: 1357-0560            Impact factor:   3.064


  16 in total

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Review 3.  Monitoring disease response to tyrosine kinase inhibitor therapy in CML.

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Journal:  Antioxid Redox Signal       Date:  2008-11       Impact factor: 8.401

Review 5.  Oxidative stress in the regulation of normal and neoplastic hematopoiesis.

Authors:  Saghi Ghaffari
Journal:  Antioxid Redox Signal       Date:  2008-11       Impact factor: 8.401

6.  PHA-680626 exhibits anti-proliferative and pro-apoptotic activity on Imatinib-resistant chronic myeloid leukemia cell lines and primary CD34+ cells by inhibition of both Bcr-Abl tyrosine kinase and Aurora kinases.

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7.  BCR-ABL maintains resistance of chronic myelogenous leukemia cells to apoptotic cell death.

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9.  Enhanced BCR-ABL kinase inhibition does not result in increased inhibition of downstream signaling pathways or increased growth suppression in CML progenitors.

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Journal:  Leukemia       Date:  2008-02-14       Impact factor: 11.528

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  5 in total

Review 1.  Overcoming challenges of ovarian cancer stem cells: novel therapeutic approaches.

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2.  miR-153 sensitized the K562 cells to As2O3-induced apoptosis.

Authors:  Li Liu; Renan Chen; Siyong Huang; Yanlan Wu; Guohui Li; Bei Zhang; Qiang Liu; Dandan Yin; Yingmin Liang
Journal:  Med Oncol       Date:  2011-01-26       Impact factor: 3.064

Review 3.  Mitochondrial membrane potential and reactive oxygen species in cancer stem cells.

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Journal:  Fam Cancer       Date:  2015-03       Impact factor: 2.375

Review 4.  Manganese superoxide dismutase in cancer prevention.

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Journal:  Antioxid Redox Signal       Date:  2013-07-18       Impact factor: 8.401

5.  Quantitative phenotyping-based in vivo chemical screening in a zebrafish model of leukemia stem cell xenotransplantation.

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  5 in total

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