Imatinib mesylate induces apoptosis of K562 cell by down-regulating miR-139

被引:0
作者
Wang, Linhui [1 ]
Guo, Pengxiang [1 ]
机构
[1] Peoples Hosp Guizhou Prov, Dept Hematol, 83 Zhongshan East Rd, Guiyang 550001, Guizhou, Peoples R China
关键词
Imatinib mesylate; microRNA-139; K562; cells; leukemia; cell apoptosis; CHRONIC MYELOID-LEUKEMIA; CHRONIC MYELOGENOUS LEUKEMIA; RESISTANCE; INHIBITOR; PATHWAY; KINASE; COMBINATION; ACTIVATION; EXPRESSION; SURVIVAL;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Leukemia has severely endangered people healthy. Imatinib mesylate is a newly-developed targeting drug for treating leukemia. This study aimed to investigate the molecular mechanism of imatinib mesylate on regulating K562 cell apoptosis via mediating micro RNA-139 (miR-139) expression. K562 cells were treated with imatinib mesylate and were examined for their growth, proliferation and apoptosis by flow cytometry. MiR-139 expression level was determined by RT-PCR. We also synthesized miR-139 expressing vectors and transfected them into K562 cells, followed by imatinib mesylate treatment and cell viability and apoptotic assays. The inhibition of K562 cell growth and proliferation occurred after imatinib mesylate treatment, accompanied with cell apoptosis. In leukemia patient sample, the expression level of miR-139 was significantly higher than normal people. K562 cell over-expressing miR-139 had depressed level of imatinib mesylate-induced cell apoptosis. Imatinib mesylate induces the apoptosis of K562 cells via suppressing miR-139 expression.
引用
收藏
页码:7863 / 7869
页数:7
相关论文
共 25 条
[1]   A polymethoxyflavone from Laggera pterodonta induces apoptosis in imatinib-resistant K562R cells via activation of the intrinsic apoptosis pathway [J].
Cao, Changshu ;
Liu, Bailian ;
Zeng, Chengwu ;
Lu, Yuhong ;
Chen, Shaohua ;
Yang, Lijian ;
Li, Bo ;
Li, Yaolan ;
Li, Yangqiu .
CANCER CELL INTERNATIONAL, 2014, 14
[2]   Methylation analysis of the DAPK1 gene in imatinib-resistant chronic myeloid leukemia patients [J].
Celik, Selcen ;
Akcora, Dilara ;
Ozkan, Tulin ;
Varol, Nuray ;
Aydos, Sena ;
Sunguroglu, Asuman .
ONCOLOGY LETTERS, 2015, 9 (01) :399-404
[3]   Morgana acts as an oncosuppressor in chronic myeloid leukemia [J].
Di Savino, Augusta ;
Panuzzo, Cristina ;
Rocca, Stefania ;
Familiari, Ubaldo ;
Piazza, Rocco ;
Crivellaro, Sabrina ;
Carra, Giovanna ;
Ferretti, Roberta ;
Fusella, Federica ;
Giugliano, Emilia ;
Camporeale, Annalisa ;
Franco, Irene ;
Miniscalco, Barbara ;
Cutrin, Juan Carlos ;
Turco, Emilia ;
Silengo, Lorenzo ;
Hirsch, Emilio ;
Rege-Cambrin, Giovanna ;
Gambacorti-Passerini, Carlo ;
Pandolfi, Pier Paolo ;
Papotti, Mauro ;
Saglio, Giuseppe ;
Tarone, Guido ;
Morotti, Alessandro ;
Brancaccio, Mara .
BLOOD, 2015, 125 (14) :2245-2253
[4]   CD-200 induces apoptosis and inhibits Bcr-Abl signaling in imatinib-resistant chronic myeloid leukemia with T315I mutation [J].
Fang, Zhenghuan ;
Jung, Kyung Hee ;
Yan, Hong Hua ;
Kim, Soo Jung ;
Son, Mi Kwon ;
Rumman, Marufa ;
Lee, Hyunseung ;
Kim, Ki Woon ;
Yoo, Hye-Dong ;
Hong, Soon-Sun .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2015, 47 (01) :253-261
[5]   Apoptosis-Related Gene Expression Profile in Chronic Myeloid Leukemia Patients after Imatinib Mesylate and Dasatinib Therapy [J].
Ferreira, Aline Fernanda ;
de Oliveira, Gislane L. V. ;
Tognon, Raquel ;
Collassanti, Maria Dulce S. ;
Zanichelli, Maria Aparecida ;
Hamerschlak, Nelson ;
de Souza, Ana Maria ;
Covas, Dimas Tadeu ;
Kashima, Simone ;
de Castro, Fabiola Attie .
ACTA HAEMATOLOGICA, 2015, 133 (04) :354-364
[6]   Curcumin potentiates the anti-leukemia effects of imatinib by downregulation of the AKT/mTOR pathway and BCR/ABL gene expression in Ph plus acute lymphoblastic leukemia [J].
Guo, Yong ;
Li, Yi ;
Shan, Qingqing ;
He, Guangcui ;
Lin, Juan ;
Gong, Yuping .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2015, 65 :1-11
[7]   Knockdown of c-MET induced apoptosis in ABCB1-overexpressed multidrug-resistance cancer cell lines [J].
Hung, T-H ;
Li, Y-H ;
Tseng, C-P ;
Lan, Y-W ;
Hsu, S-C ;
Chen, Y-H ;
Huang, T-T ;
Lai, H-C ;
Chen, C-M ;
Choo, K-B ;
Chong, K-Y .
CANCER GENE THERAPY, 2015, 22 (05) :262-270
[8]   Korean Red Ginseng Extract Enhances the Anticancer Effects of Imatinib Mesylate Through Abrogation p38 and STAT5 Activation in KBM-5 Cells [J].
Jung, Sang Yoon ;
Kim, Chulwon ;
Kim, Wan-Seok ;
Lee, Seok-Geun ;
Lee, Jun-Hee ;
Shim, Bum Sang ;
Kim, Sung-Hoon ;
Ahn, Kyoo Seok ;
Ahn, Kwang Seok .
PHYTOTHERAPY RESEARCH, 2015, 29 (07) :1062-1072
[9]   Non-receptor tyrosine kinase inhibitors enhances β-cell survival by suppressing the PKCδ signal transduction pathway in streptozotocin - induced β-cell apoptosis [J].
Karunakaran, Udayakumar ;
Park, Si Jun ;
Jun, Do Youn ;
Sim, Taebo ;
Park, Keun-Gyu ;
Kim, Myoung Ok ;
Lee, In Kyu .
CELLULAR SIGNALLING, 2015, 27 (06) :1066-1074
[10]   Revealing genome-wide mRNA and microRNA expression patterns in leukemic cells highlighted "hsa-miR-2278" as a tumor suppressor for regain of chemotherapeutic imatinib response due to targeting STAT5A [J].
Kaymaz, Burcin Tezcanli ;
Gunel, Nur Selvi ;
Ceyhan, Metin ;
Cetintas, Vildan Bozok ;
Ozel, Buket ;
Yandim, Melis Kartal ;
Kipcak, Sezgi ;
Aktan, Cagdas ;
Gokbulut, Aysun Adan ;
Baran, Yusuf ;
Can, Buket Kosova .
TUMOR BIOLOGY, 2015, 36 (10) :7915-7927