ハギハラ カナコ
Hagihara Kanako
萩原 加奈子 所属 兵庫医科大学 薬学部 医療薬学科 職種 助教 |
|
言語種別 | 英語 |
発行・発表の年月 | 2017/07 |
形態種別 | 学術雑誌 |
査読 | 査読あり |
標題 | Identification of ACA-28, a 1'-acetoxychavicol acetate analogue compound, as a novel modulator of ERK MAPK signaling, which preferentially kills human melanoma cells. |
執筆形態 | 共著 |
掲載誌名 | Genes to cells : devoted to molecular & cellular mechanisms |
掲載区分 | 国外 |
巻・号・頁 | 22(7),pp.608-618 |
著者・共著者 | Satoh Ryosuke, Hagihara Kanako, Matsuura Kazuki, Manse Yoshiaki, Kita Ayako, Kunoh Tatsuki, Masuko Takashi, Moriyama Mariko, Moriyama Hiroyuki, Tanabe Genzoh, Muraoka Osamu, Sugiura Reiko |
概要 | Here, we carried out a chemical genetic screen using a fission yeast phenotypic assay and showed that ACA-28, a synthetic derivative of 1'-acetoxychavicol acetate (ACA), which is a natural ginger compound, effectively inhibited the growth of melanoma cancer cells wherein ERK MAPK signaling is hyperactivated due to mutations in the upstream activating regulators. ACA-28 more potently inhibited the growth of melanoma cells than did the parental compound ACA. Importantly, the growth of normal human epidermal melanocytes (NHEM) was less affected by ACA-28 at the same 50% inhibitory concentration. In addition, ACA-28 specifically induced apoptosis in NIH/3T3 cells which were oncogenically transformed with human epidermal growth factor receptor-2 (HER2/ErbB2), but not in the parental cells. ACA-28 might serve as a promising seed compound for melanoma treatment. |
DOI | 10.1111/gtc.12499 |
ISSN | 1365-2443 |
PMID | 28485554 |