TY - JOUR
T1 - Overexpression of IL-1ra gene up-regulates interleukin-1β converting enzyme (ICE) gene expression
T2 - Possible mechanism underlying IL-1β-resistance of cancer cells
AU - Sumitomo, M.
AU - Tachibana, M.
AU - Murai, M.
AU - Hayakawa, M.
AU - Nakamura, H.
AU - Takayanagi, A.
AU - Shimizu, N.
N1 - Funding Information:
This work was supported in part by grants-in-aid Nos 07407046 and 10146673 for Scientific Research from the Ministry of Education, Science and Sport Culture, Japan.
PY - 1999
Y1 - 1999
N2 - We investigated the interaction of endogenous interleukin (IL)-1β, IL-1ra, and interleukin-1β converting enzyme (ICE) in four human urological cancer cell lines, KU-19-19, KU-1, KU-2 and KU-19-20. Northern blot analysis showed that IL-1β gene was expressed in all call lines. On the other hand, in KU-19-19 and KU-19-20, the gene expressions of both IL-1ra and ICE were suppressed. MTT assay revealed that IL-1β (10 ng ml-1) promoted cell growth in KU-19-19 and KU-19-20, while it inhibited in KU-1 and KU-2. An ICE inhibitor, Acetyl-Tyr-Val-Ala-Asp-CHO (YVAD-CHO) blocked IL-1β-induced growth inhibition in KU-1 and KU-2. Overexpression of the secretory type IL-1ra with adenovirus vector (AxIL-1ra) Enhanced ICE gene expression, while exogenous IL-1ra (100 ng ml-1) did not enhance it. Furthermore, AxIL-1ra treatment promoted endogenous IL-1β secretion and induced significant growth inhibition and apoptotic cell death on KU-19-19 and KU-19-20. Treatment with either IL-1ra (100 ng ml-1), IL-1β antibody (100 μg ml-1), or YVAD-CHO blocked AxlL-1ra-induced cell death in KU-19-19 and KU-19-20. These results suggest that IL-1β-sensitivity depends on the level of ICE gene expression, which is regulated by the level of endogenous sIL-1ra expression. This is a first report on the intracellular junction of sIL-1ra and these findings may provide key insights into the mechanism underlying the viability of cancer cells.
AB - We investigated the interaction of endogenous interleukin (IL)-1β, IL-1ra, and interleukin-1β converting enzyme (ICE) in four human urological cancer cell lines, KU-19-19, KU-1, KU-2 and KU-19-20. Northern blot analysis showed that IL-1β gene was expressed in all call lines. On the other hand, in KU-19-19 and KU-19-20, the gene expressions of both IL-1ra and ICE were suppressed. MTT assay revealed that IL-1β (10 ng ml-1) promoted cell growth in KU-19-19 and KU-19-20, while it inhibited in KU-1 and KU-2. An ICE inhibitor, Acetyl-Tyr-Val-Ala-Asp-CHO (YVAD-CHO) blocked IL-1β-induced growth inhibition in KU-1 and KU-2. Overexpression of the secretory type IL-1ra with adenovirus vector (AxIL-1ra) Enhanced ICE gene expression, while exogenous IL-1ra (100 ng ml-1) did not enhance it. Furthermore, AxIL-1ra treatment promoted endogenous IL-1β secretion and induced significant growth inhibition and apoptotic cell death on KU-19-19 and KU-19-20. Treatment with either IL-1ra (100 ng ml-1), IL-1β antibody (100 μg ml-1), or YVAD-CHO blocked AxlL-1ra-induced cell death in KU-19-19 and KU-19-20. These results suggest that IL-1β-sensitivity depends on the level of ICE gene expression, which is regulated by the level of endogenous sIL-1ra expression. This is a first report on the intracellular junction of sIL-1ra and these findings may provide key insights into the mechanism underlying the viability of cancer cells.
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U2 - 10.1038/sj.bjc.6690688
DO - 10.1038/sj.bjc.6690688
M3 - Article
C2 - 10496353
AN - SCOPUS:0032833649
SN - 0007-0920
VL - 81
SP - 277
EP - 286
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 2
ER -