RETRACTED: Reversal Effect of ST6GAL 1 on Multidrug Resistance in Human Leukemia by Regulating the PI3K/Akt Pathway and the Expression of P-gp and MRP1 (Retracted Article)

被引:41
|
作者
Ma, Hongye [1 ]
Cheng, Lei [2 ]
Hao, Keji [3 ]
Li, Yanping [1 ]
Song, Xiaobo [4 ]
Zhou, Huimin [5 ]
Jia, Li [1 ]
机构
[1] Med Univ, Coll Lab Med, Dalian, Liaoning Provin, Peoples R China
[2] Dalian Med Univ, Affiliated Hosp 1, Dept Laparoscop Surg, Dalian, Liaoning Provin, Peoples R China
[3] Peking Univ, Peoples Hosp, Dept Nucl Med, Beijing 100871, Peoples R China
[4] Univ Tromso, Fac Hlth Sci, Dept Med Biol, Tromso, Norway
[5] Dalian Med Univ, Dept Microbiol, Dalian, Liaoning Provin, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 01期
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; BETA-GALACTOSIDE ALPHA-2,6-SIALYLTRANSFERASES; ACUTE LYMPHOBLASTIC-LEUKEMIA; COLON-CARCINOMA CELLS; COLORECTAL-CANCER; GASTRIC-CANCER; IN-VITRO; ACTIVATION; GLYCOPROTEIN; INHIBITOR;
D O I
10.1371/journal.pone.0085113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
beta-galactoside alpha 2, 6-sialyltransferse gene (ST6GAL) family has two members, which encode corresponding enzymes ST6Gal I and ST6Gal II. The present atudy was to investigate whether and how ST6GAL family involved in multidrug resistance (MDR) in human leukemia cell lines and bone marrow mononuclear cells (BMMC) of leukemia patients. Real-time PCR showed a high expression level of ST6GAL1 gene in both MDR cells and BMMCs (*P<0.05). Alternation of ST6GAL1 levels had a significant impact on drug-resistant phenotype changing of K562 and K562/ADR cells both in vitro and in vivo. However, no significant changes were observed of ST6GAL2 gene. Further data revealed that manipulation of ST6GAL1 modulated the activity of phosphoinositide 3 kinase (PI3K)/Akt signaling and consequently regulated the expression of P-glycoprotein (P-gp, *P<0.05) and multidrug resistance related protein 1 (MRP1, *P<0.05), which are both known to be associated with MDR. Therefore we postulate that ST6GAL1 is responsible for the development of MDR in human leukemia cells probably through medicating the activity of PI3K/Akt signaling and the expression of P-gp and MRP1.
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页数:11
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