Literature DB >> 18459962

Possible involvement of caspase-7 in cell cycle progression at mitosis.

Toshiaki Hashimoto1, Lisa Yamauchi, Tony Hunter, Ushio Kikkawa, Shinji Kamada.   

Abstract

Caspases are suggested to play essential roles not only in apoptotic but also in non-apoptotic functions. However, the contribution of caspases to the cell cycle regulation is unclear. Here we found that caspases including caspase-3, caspase-7, caspase-8 and caspase-9 were activated during mitosis. Chemically synthesized caspase inhibitors delayed mitotic progression and induced accumulation of mitotic cells, which exhibited abnormal chromatin condensation and incomplete chromosome segregation. Furthermore, knockdown of caspase-7 by using small interfering RNAs resulted in the inhibition of cell proliferation, but knockdown of other caspases did not show a significant effect on cell growth. The expression of short hairpin RNA directed against caspase-7 induced the cell cycle arrest at mitosis, which was rescued by the re-expression of caspase-7 containing silent mutations at the target site for the short hairpin RNA. These results revealed that caspase-7 has a novel role during cell cycle progression at mitosis.

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Year:  2008        PMID: 18459962     DOI: 10.1111/j.1365-2443.2008.01192.x

Source DB:  PubMed          Journal:  Genes Cells        ISSN: 1356-9597            Impact factor:   1.891


  17 in total

1.  Regulation of caspase pathways by protein kinase CK2: identification of proteins with overlapping CK2 and caspase consensus motifs.

Authors:  Jacob P Turowec; James S Duncan; Greg B Gloor; David W Litchfield
Journal:  Mol Cell Biochem       Date:  2011-07-13       Impact factor: 3.396

2.  Endocrine resistant breast cancer cells with loss of ERα expression retain proliferative ability by reducing caspase7-mediated HDAC3 cleavage.

Authors:  Shiyi Yu; Xue Gong; Zhifang Ma; Meng Zhang; Ling Huang; Jun Zhang; Shuang Zhao; Tao Zhu; Zhenghong Yu; Liming Chen
Journal:  Cell Oncol (Dordr)       Date:  2019-11-07       Impact factor: 6.730

3.  Proliferating γδ T cells manifest high and spatially confined caspase-3 activity.

Authors:  Andreas Koenig; Karen A Fortner; Benjamin R King; Jonathan Madden; Iwona A Buskiewicz; Ralph C Budd
Journal:  Immunology       Date:  2012-04       Impact factor: 7.397

4.  Non-apoptotic function of apoptotic proteins in the development of Malpighian tubules of Drosophila melanogaster.

Authors:  Madhu G Tapadia; Naveen K Gautam
Journal:  J Biosci       Date:  2011-08       Impact factor: 1.826

5.  SAHA and EGCG Promote Apoptosis in Triple-negative Breast Cancer Cells, Possibly Through the Modulation of cIAP2.

Authors:  Kayla L Steed; Harrison R Jordan; Trygve O Tollefsbol
Journal:  Anticancer Res       Date:  2020-01       Impact factor: 2.480

6.  Interception Targets of Angelica Gigas Nakai Root Extract versus Pyranocoumarins in Prostate Early Lesions and Neuroendocrine Carcinomas in TRAMP Mice.

Authors:  Su-Ni Tang; Peixin Jiang; Sangyub Kim; Jinhui Zhang; Cheng Jiang; Junxuan Lü
Journal:  Cancer Prev Res (Phila)       Date:  2021-03-01

7.  Development of high content imaging methods for cell death detection in human pluripotent stem cell-derived cardiomyocytes.

Authors:  Maxime Mioulane; Gabor Foldes; Nadire N Ali; Michael D Schneider; Sian E Harding
Journal:  J Cardiovasc Transl Res       Date:  2012-08-16       Impact factor: 4.132

8.  Caspase activity is not required for the mitotic checkpoint or mitotic slippage in human cells.

Authors:  Kyunghee Lee; Alison E Kenny; Conly L Rieder
Journal:  Mol Biol Cell       Date:  2011-05-25       Impact factor: 4.138

9.  Contribution of caspase(s) to the cell cycle regulation at mitotic phase.

Authors:  Toshiaki Hashimoto; Ushio Kikkawa; Shinji Kamada
Journal:  PLoS One       Date:  2011-03-30       Impact factor: 3.240

10.  Preferential Fas-mediated apoptotic execution at G1 phase: the resistance of mitotic cells to the cell death.

Authors:  T Hashimoto; K Juso; M Nakano; T Nagano; S Kambayashi; A Nakashima; U Kikkawa; S Kamada
Journal:  Cell Death Dis       Date:  2012-05-24       Impact factor: 8.469

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