ミツイシ ツヨシ
  三石 剛
   所属   医学部 医学科(附属八千代医療センター)
   職種   准教授
論文種別 原著
言語種別 英語
査読の有無 査読あり
表題 Activation of STAT5 confers imatinib resistance on leukemic cells through the transcription of TERT and MDR1.
掲載誌名 正式名:Cellular signalling
略  称:Cell Signal
ISSNコード:1873-3913(Electronic)0898-6568(Linking)
巻・号・頁 23(7),1119-27頁
著者・共著者 Yamada Osamu, Ozaki Kohji, Furukawa Thoru, Machida Mitsuyo, Wang Yan-Hua, Motoji Toshiko, Mitsuishi Tsuyoshi, Akiyama Masaharu, Yamada Hisashi, Kawauchi Kiyotaka, Matsuoka Rumiko
発行年月 2011/07
概要 We used two imatinib resistant cell lines, K562-ADM cells, which over-express P-glycoprotein (a product of the ABCB1 gene, more commonly known as MDR1), and K562-hTERT cells, which over-express the telomerase reverse transcriptase (TERT), as models to show that the acquisition of multidrug resistance in CML is associated with the enhanced phosphorylation of signal transducer and activator of transcription 5 (STAT5). The induction of P-glycoprotein expression that occurred in response to adriamycin treatment was accompanied by increased phosphorylation of BCR-ABL and STAT5, as well as increased telomerase protein expression. Intriguingly, a ChIP assay using an anti-STAT5 antibody revealed direct binding of STAT5 to the promoter regions of both the human TERT gene and the MDR1 gene in K562-ADM cells. Conversely, silencing of endogenous STAT5 expression by siRNA significantly reduced both the expression of P-glycoprotein and telomerase activity and resulted in the recovery of the imatinib sensitivity of K562-ADM cells. These findings indicate a critical role for STAT5 in the induction of P-glycoprotein and in the modulation of telomerase activity in drug-resistant CML cells. Furthermore, primary leukemic cells obtained from patients in blast crisis showed increased levels of phospho-STAT5, P-glycoprotein and telomerase.In contrast, none of these proteins were detectable in the cells obtained from patients in the chronic phase. Together, these findings indicate a novel mechanism that contributes toward multidrug resistance involving STAT5 as a sensor for cytotoxic drugs in CML patients.
DOI 10.1016/j.cellsig.2011.02.005
文献番号 21356308