| Literature DB >> 24900207 |
Hiroyuki Yamakoshi1, Naoki Kanoh1, Chieko Kudo2, Atsuko Sato2, Kazunori Ueda1, Makoto Muroi3, Shunsuke Kon2, Masanobu Satake2, Hisatsugu Ohori2, Chikashi Ishioka2, Yoshiteru Oshima1, Hiroyuki Osada3, Natsuko Chiba2, Hiroyuki Shibata4, Yoshiharu Iwabuchi1.
Abstract
Bis(arylmethylidene)acetone derivatives are an important class of curcumin analogues that exhibit various biological and pharmacological activities. We herein report that GO-Y086, a biotinylated bis(arylmethylidene)acetone, inhibits cancer cell growth. We also show that GO-Y086 specifically interacts with the nuclear protein KSRP/FUBP2 by covalent modification. GO-Y086 markedly suppresses the expression of the c-Myc protein, which plays an important role in cellular proliferation and whose expression is regulated by KSRP/FUBP2.Entities:
Keywords: KSRP/FUBP2; anticancer; bis(arylmethylidene)acetone; c-Myc; curcumin analogue; target protein
Year: 2010 PMID: 24900207 PMCID: PMC4007841 DOI: 10.1021/ml1000454
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345