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Induction of endoreduplication by a JNK inhibitor SP600125 in human lung carcinoma A 549 cells
Author(s) -
MiyamotoYamasaki Yumi,
Yamasaki Masao,
Tachibana Hirofumi,
Yamada Koji
Publication year - 2007
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1016/j.cellbi.2007.07.002
Subject(s) - endoreduplication , cell cycle , cell cycle checkpoint , cell growth , downregulation and upregulation , kinase , microbiology and biotechnology , a549 cell , cell , chemistry , cancer research , biology , biochemistry , gene
The effect of the pan c‐Jun N‐terminal kinase (JNK) inhibitor SP600125 on the proliferation of human lung carcinoma A549 cells has been evaluated. We have shown that SP600125 completely inhibited the proliferation of A549 cells, the cycle arrest being in G2/M phase. When cells were treated with SP600125 for >12 h, a cell population with DNA content of 4n to 8n was detected. Moreover, the effect of SP600125 on the expression of cell cycle related proteins was an upregulation of p53 protein accompanied by an increase in its molecular mass. Prolonged SP600125 treatment downregulated p21, Bax and Mdm2 expression, but increased the level of the cellular p53–Mdm2 complex. Taken together, we show that SP600125 could induce G2/M cell cycle arrest and endoreduplication in a p21 independent manner, and that SP600125 could also post‐translationally modify p53 to modify its function. Our data show that basic JNK activity plays an important role in the progression of the cell cycle at G2/M cell phase.