TY - JOUR
T1 - Novel biological response modifiers
T2 - Phthalimides with TNF-α production regulating activity
AU - Miyachi, Hiroyuki
AU - Azuma, Akihiko
AU - Hashimoto, Yuichi
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1997/2
Y1 - 1997/2
N2 - Tumor necrosis factor alpha (TNF-α), an important cytokine produced mainly by activated macrophages, plays a critical role in certain physiological immune systems. But it causes severe damage to the host when produced in excess. Therefore, TNF-α can be regarded to possess both favorable and unfavorable effects. These pleiotropic effects indicated that TNF-α production-enhancers in some cases and TNF-α production-inhibitors in other cases would be useful as biological response modifiers (BRMs) under various circumstances. A possible lead compound is thalidomide, which had been used as a hypnotic/sedative agents but was withdrawn from the market because of it's teratogenicity. Thalidomide is a specific inhibitor of TNF- α production, and this effect has been shown to be useful for the treatment of various immunodiseases. Recently, we found that the regulation of TNF-α production by thalidomide and related phthalimides was both inducer-specific and cell-type-specific, i.e., (I) the compounds enhance 12-O- tetradecanoylphorbol 13-acetate (TPA)-induced TNF-α production by HL-60 cells, while they inhibit TPA-induced TNF-α production by another human leukemia cell line THP-1, and (II) the compounds inhibit TNF-α production both by HL-60 and THP-1 cells when the cells are stimulated with okadaic acid. We also found that in a optically active phthalimide analogues of thalidomide the inducer specific bi-directional regulation of TNF-α production is separated. This implies that the target molecule(s) of the two systems are different each other.
AB - Tumor necrosis factor alpha (TNF-α), an important cytokine produced mainly by activated macrophages, plays a critical role in certain physiological immune systems. But it causes severe damage to the host when produced in excess. Therefore, TNF-α can be regarded to possess both favorable and unfavorable effects. These pleiotropic effects indicated that TNF-α production-enhancers in some cases and TNF-α production-inhibitors in other cases would be useful as biological response modifiers (BRMs) under various circumstances. A possible lead compound is thalidomide, which had been used as a hypnotic/sedative agents but was withdrawn from the market because of it's teratogenicity. Thalidomide is a specific inhibitor of TNF- α production, and this effect has been shown to be useful for the treatment of various immunodiseases. Recently, we found that the regulation of TNF-α production by thalidomide and related phthalimides was both inducer-specific and cell-type-specific, i.e., (I) the compounds enhance 12-O- tetradecanoylphorbol 13-acetate (TPA)-induced TNF-α production by HL-60 cells, while they inhibit TPA-induced TNF-α production by another human leukemia cell line THP-1, and (II) the compounds inhibit TNF-α production both by HL-60 and THP-1 cells when the cells are stimulated with okadaic acid. We also found that in a optically active phthalimide analogues of thalidomide the inducer specific bi-directional regulation of TNF-α production is separated. This implies that the target molecule(s) of the two systems are different each other.
KW - phthalimide
KW - thalidomide
KW - tumor necrosis factor
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U2 - 10.1248/yakushi1947.117.2_91
DO - 10.1248/yakushi1947.117.2_91
M3 - Article
C2 - 9084226
AN - SCOPUS:0030945515
SN - 0031-6903
VL - 117
SP - 91
EP - 107
JO - Yakugaku Zasshi
JF - Yakugaku Zasshi
IS - 2
ER -