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IL-6-induced Bcl6 variant 2 supports IL-6-dependent myeloma cell proliferation and survival through STAT3
被引:23
作者:
Tsuyama, N
Danjoh, I
Otsuyama, K
Obata, M
Tahara, H
Ohta, T
Ishikawa, H
机构:
[1] Yamaguchi Univ, Grad Sch Med, Dept Bio Signal Analysis, Ube, Yamaguchi 7558505, Japan
[2] Yamaguchi Univ, Grad Sch Med, Dept Bio Signal Analysis, Ube, Yamaguchi 7558505, Japan
[3] Natl Canc Ctr, Res Inst, Ctr Med Genom, Div Genet,Chuo Ku, Tokyo 104, Japan
[4] Hiroshima Univ, Grad Sch Med, Dept Cellular & Mol Biol, Hiroshima 7320001, Japan
关键词:
myeloma;
IL-6;
microarray;
Bcl6;
STAT3;
p53;
PDCD4;
trichostatin A;
D O I:
10.1016/j.bbrc.2005.09.036
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
IL-6 is a growth and survival factor for myeloma cells, although the mechanism by which it induces myeloma cell proliferation through gene expression is largely unknown. Microarray analysis showed that some B-cell lymphoma-associated oncogenes such as Bc16, which is absent in normal plasma cells, were upregulated by IL-6 in IL-6-dependent myeloma cell lines. We found that Bc16 variant 2 was upregulated by STAT3. ChIP assay and EMSA showed that STAT3 bound to the upstream region of variant 2 DNA. Expression of p53, a direct target gene of Bc16, was downregulated in the IL-6-stimulated cells, and this process was impaired by an HDAC inhibitor. Bc16 was knocked down by introducing small hairpin RNA, resulting in decreased proliferation and increased sensitivity to a DNA damaging agent. Thus, STAT3-inducible Bc16 variant 2 appears to generate an important IL-6 signal that supports proliferation and survival of IL-6-dependent myeloma cells. (c) 2005 Elsevier Inc. All rights reserved.
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页码:201 / 208
页数:8
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