Literature DB >> 15587394

Arsenic trioxide inhibits proliferation in K562 cells by changing cell cycle and survivin expression.

Xiaofei Wu1, Zhichao Chen, Zhongping Liu, Hao Zhou, Yong You, Weiming Li, Ping Zou.   

Abstract

To study the mechanisms involved in the inhibition of chronic myeloid leukemic cells (K562) proliferation induced by arsenic trioxide (As2O3) and to explore the potential role of Survivin, an inhibitor of apoptosis protein, in the regulation of As2O3 induced cell apoptosis, K562 cells were cultured with As2O3 of different concentrations. Cells were collected for proliferation analysis by MTT assay. Cell cycle distribution and cell apoptosis were analyzed by flow cytometry. Expression of Survivin protein and mRNA were detected by flow cytometry and RT-PCR, respectively. Our results showed that As2O3(2-10 micromol/L) inhibited K562 cells growth effectively, but it did not induce cells apoptosis significantly. The percentage of K562 cells at G2/M phase increased in proportion to As2O3 concentrations, and the expression of Survivin mRNA and content of Survivin protein was up-regulated accordingly. It is concluded that As2O3 inhibited K562 cells growth by inducing cell cycle arrest mainly at G2/M phase. Over-expression of Survivin gene and protein might be one of the possible mechanisms contributing to K562 cells' resistance to As2O3-induced apoptosis.

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Year:  2004        PMID: 15587394     DOI: 10.1007/bf02861863

Source DB:  PubMed          Journal:  J Huazhong Univ Sci Technolog Med Sci        ISSN: 1672-0733


  6 in total

1.  An anti-apoptotic protein human survivin is a direct inhibitor of caspase-3 and -7.

Authors:  S Shin; B J Sung; Y S Cho; H J Kim; N C Ha; J I Hwang; C W Chung; Y K Jung; B H Oh
Journal:  Biochemistry       Date:  2001-01-30       Impact factor: 3.162

2.  The induction of apoptosis and cell cycle arrest by arsenic trioxide in lymphoid neoplasms.

Authors:  W Zhang; K Ohnishi; K Shigeno; S Fujisawa; K Naito; S Nakamura; K Takeshita; A Takeshita; R Ohno
Journal:  Leukemia       Date:  1998-09       Impact factor: 11.528

3.  Dual effects of arsenic trioxide (As2O3) on non-acute promyelocytic leukaemia myeloid cell lines: induction of apoptosis and inhibition of proliferation.

Authors:  M T Rojewski; C Baldus; W Knauf; E Thiel; H Schrezenmeier
Journal:  Br J Haematol       Date:  2002-03       Impact factor: 6.998

4.  Arsenic trioxide arrests cells early in mitosis leading to apoptosis.

Authors:  H Dorota Halicka; Piotr Smolewski; Zbigniew Darzynkiewicz; Wei Dai; Frank Traganos
Journal:  Cell Cycle       Date:  2002 May-Jun       Impact factor: 4.534

5.  The ubiquitin-proteasome pathway regulates survivin degradation in a cell cycle-dependent manner.

Authors:  J Zhao; T Tenev; L M Martins; J Downward; N R Lemoine
Journal:  J Cell Sci       Date:  2000-12       Impact factor: 5.285

6.  Control of apoptosis and mitotic spindle checkpoint by survivin.

Authors:  F Li; G Ambrosini; E Y Chu; J Plescia; S Tognin; P C Marchisio; D C Altieri
Journal:  Nature       Date:  1998-12-10       Impact factor: 49.962

  6 in total
  2 in total

1.  BH3-only proteins Noxa, Bmf, and Bim are necessary for arsenic trioxide-induced cell death in myeloma.

Authors:  Alejo A Morales; Delia Gutman; Kelvin P Lee; Lawrence H Boise
Journal:  Blood       Date:  2008-03-19       Impact factor: 22.113

2.  Arsenic trioxide induces a beclin-1-independent autophagic pathway via modulation of SnoN/SkiL expression in ovarian carcinoma cells.

Authors:  D M Smith; S Patel; F Raffoul; E Haller; G B Mills; M Nanjundan
Journal:  Cell Death Differ       Date:  2010-05-28       Impact factor: 15.828

  2 in total

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