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Nucleostemin Depletion Induces Post-g1 Arrest Apoptosis in Chronic Myelogenous Leukemia K562 Cells

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Journal Adv Pharm Bull
Date 2014 Jan 11
PMID 24409410
Citations 7
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Abstract

Purpose: Despite significant improvements in treatment of chronic myelogenous leukemia (CML), the emergence of leukemic stem cell (LSC) concept questioned efficacy of current therapeutical protocols. Remaining issue on CML includes finding and targeting of the key genes responsible for self-renewal and proliferation of LSCs. Nucleostemin (NS) is a new protein localized in the nucleolus of most stem cells and tumor cells which regulates their self-renewal and cell cycle progression. The aim of this study was to investigate effects of NS knocking down in K562 cell line as an in vitro model of CML.

Methods: NS gene silencing was performed using a specific small interfering RNA (NS-siRNA). The gene expression level of NS was evaluated by RT-PCR. The viability and growth rate of K562 cells were determined by trypan blue exclusion test. Cell cycle distribution of the cells was analyzed by flow cytometry.

Results: Our results showed that NS knocking down inhibited proliferation and viability of K562 cells in a time-dependent manner. Cell cycle studies revealed that NS depletion resulted in G(1) cell cycle arrest at short times of transfection (24 h) followed with apoptosis at longer times (48 and 72 h), suggest that post-G1 arrest apoptosis is occurred in K562 cells.

Conclusion: Overall, these results point to essential role of NS in K562 cells, thus, this gene might be considered as a promising target for treatment of CML.

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Silencing of Nucleostemin by siRNA Induces Apoptosis in MCF-7 and MDA-MB-468 Cell Lines.

Moudi M, Saravani R, Sargazi S Iran J Pharm Res. 2020; 19(1):37-45.

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Cytokines secreted from bone marrow derived mesenchymal stem cells promote apoptosis and change cell cycle distribution of K562 cell line as clinical agent in cell transplantation.

Fathi E, Farahzadi R, Valipour B, Sanaat Z PLoS One. 2019; 14(4):e0215678.

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Differential expression of nucleostemin in the cytoplasm and nuclei of normal and cancerous cell lines.

Kavyasudha C, Joel J, Devi A Turk J Biol. 2019; 42(3):250-258.

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