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4篇 您的检索式:作者名="MAKOTO KAWATANI"
    题名 作者 年代 出处 被引量
1Transmembrane domain of Bcl -2 is required for hlhibition of ceramide synthesis, but not cytochrome release in the pathway nf inostamycin - induced apoptosis显示文摘Makoto Kawatani Madoka Uchi Siro Simizu 2003Experimental Cell Research2003,286,1:1
2Reveromycin A,an agent for osteaporosis,inhibits bone resorption by inducing apoptosis specifically in osteoclasts显示文摘Je-Tae Woo Makoto Kawatani Masanori Kato 2006PNAS Mar2006,103,:1
3Transmembrane domain of Bcl-2 is required for inhibition of ceramide synthesis, but not cytochrome c release in the pathway of inostamycin-induced apoptosis 显示文摘Makoto Kawatani Madoka Uchi Siro Simizu 2003Exp Cell Res2003,286,1:1
4Identification of a dihydroorotate dehydrogenase inhibitor thatinhibits cancer cell growth by proteomic profiling显示文摘Dihydroorotate dehydrogenase(DHODH)is a central enzyme of the de novo pyrimidine biosynthesis pathway and is a promising drug target for the treatment of cancer and autoimmune diseases.This study presents the identification of a potent DHODH inhibitor by proteomic profiling.Cell-based screening revealed that NPD723,which is reduced to H-006 in cells,strongly induces myeloid differentiation and inhibits cell growth in HL-60 cells.H-006 also suppressed the growth of various cancer cells.Proteomic profiling of NPD723-treated cells in ChemProteoBase showed that NPD723 was clustered with DHODH inhibitors.H-006 potently inhibited human DHODH activity in vitro,whereas NPD723 was approximately 400 times less active than H-006.H-006-induced cell death was rescued by the addition of the DHODH product orotic acid.Moreover,metabolome analysis revealed that H-006 treatment promotes marked accumulation of the DHODH substrate dihydroorotic acid.These results suggest that NPD723 is reduced in cells to its active metabolite H-006,which then targets DHODH and suppresses cancer cell growth.Thus,H-006-related drugs represent a potentially powerful treatment for cancer and other diseases.MAKOTO KAWATANI HARUMI AONO SAYOKO HIRANUMA TAKESHI SHIMIZU MAKOTO MUROI TOSHIHIKO NOGAWA TOMOKAZU OHISHI SHUN-ICHI OHBA MANABU KAWADA KANAMI YAMAZAKI SHINGO DAN NAOSHI DOHMAE HIROYUKI OSADA 2023Oncology Research2023,31,6:0
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