Downregulation of NPM reverses multidrug resistance in human hepatoma cells via inhibition of P-glycoprotein expression

被引:7
作者
Luo, Fei [1 ]
Li, Huiyu [2 ]
Liang, Jianfang [3 ]
Jia, Hongyan [4 ]
Li, Xiaoyu [5 ]
Xiao, Hong [3 ]
He, Xuehua [6 ]
He, Jiefeng [2 ]
Tian, Yanzhang [2 ]
Zhao, Haoliang [2 ]
机构
[1] Shanxi Canc Hosp, Dept Breast Surg, Taiyuan 030013, Shanxi, Peoples R China
[2] Shanxi Acad Med Sci, Shanxi Dayi Hosp, Dept Gen Surg, 99 Longcheng Main St, Taiyuan 030032, Shanxi, Peoples R China
[3] Shanxi Med Univ, Dept Pathol, Hosp 1, Taiyuan 030001, Shanxi, Peoples R China
[4] Shanxi Med Univ, Dept Gen Surg, Hosp 1, Taiyuan 030001, Shanxi, Peoples R China
[5] Shanxi Canc Hosp, Dept Mol Biol, Taiyuan 030013, Shanxi, Peoples R China
[6] Shanxi Acad Med Sci Shanxi Dayi Hosp, Dept Blood Transfus, Taiyuan 030032, Shanxi, Peoples R China
关键词
hepatocellular carcinoma; multidrug resistance; nucleophosmin; p-glycoprotein; NSC348884; NUCLEAR-MATRIX PROTEIN; DRUG-RESISTANCE; HEPATOCELLULAR-CARCINOMA; CENTROSOME DUPLICATION; RIBOSOME BIOGENESIS; 3T3; FIBROBLASTS; GASTRIC-CANCER; BREAST-CANCER; UP-REGULATION; NUCLEOPHOSMIN;
D O I
10.3892/mmr.2017.6246
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multidrug resistance (MDR) is an important issue in current cancer treatments. In human cancer, drug resistance is primarily associated with the overexpression of multidrug resistance gene 1 (MDR1). Therefore, the human MDR1 gene promoter may be a target for anti-MDR drug screening. Numerous methods to prevent MDR have been investigated. However, they have been proven to be clinically ineffective. Therefore, the aim of the present study was to investigate whether downregulation of nucleophosmin (NPM) demonstrates any effects on the reversal of MDR in hepatocellular carcinoma (HCC) cells. In the present study, two invitro MDR HCC cell lines, HepG2/Adriamycin (ADM) and SMMC7721/ADM, were established and the level of MDR was measured. The results demonstrated that NPM downregulation markedly reversed the effects of MDR in the model used. In addition, NPM downregulation reduced P-glycoprotein expression, as well as MDR1 expression. These results suggested that downregulation of NPM may be a novel and effective method of reversing the effects of MDR, and may be a potential adjuvant for tumor chemotherapy.
引用
收藏
页码:2360 / 2368
页数:9
相关论文
共 50 条
  • [41] β-carotene reverses multidrug resistant cancer cells by selectively modulating human P-glycoprotein function
    Teng, Yu-Ning
    Sheu, Ming-Jyh
    Hsieh, Yow-Wen
    Wang, Ruey-Yun
    Chiang, Yao-Chang
    Hung, Chin-Chuan
    [J]. PHYTOMEDICINE, 2016, 23 (03) : 316 - 323
  • [42] Tivozanib reverses multidrug resistance mediated by ABCB1 (P-glycoprotein) and ABCG2 (BCRP)
    Yang, Danwen
    Kathawala, Rishil J.
    Chufan, Eduardo E.
    Patel, Atish
    Ambudkar, Suresh V.
    Chen, Zhe-Sheng
    Chen, Xiang
    [J]. FUTURE ONCOLOGY, 2014, 10 (11) : 1827 - 1841
  • [43] Expression of P-glycoprotein and Multidrug Resistance-associated Protein is Associated with Multidrug Resistance in Gastric Cancer
    Xu, H-W
    Xu, L.
    Hao, J-H
    Qin, C-Y
    Liu, H.
    [J]. JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2010, 38 (01) : 34 - 42
  • [44] Multidrug resistance mediated by overexpression of P-glycoprotein in human osteosarcoma in vivo
    Suto, R
    Abe, Y
    Nakamura, M
    Ohnishi, Y
    Yoshimura, M
    Lee, YH
    Imanishi, T
    Yamazaki, H
    Kijima, H
    Tokunaga, T
    Oshika, Y
    Hiraoka, N
    Tamaoki, N
    Fukuda, H
    Ueyama, Y
    [J]. INTERNATIONAL JOURNAL OF ONCOLOGY, 1998, 12 (02) : 287 - 291
  • [45] An Update on Circumventing Multidrug Resistance in Cancer by Targeting P-Glycoprotein
    Yang, Xiaoqian
    Li, Xiaoduan
    Duan, Zhenfeng
    Wang, Xipeng
    [J]. CURRENT CANCER DRUG TARGETS, 2018, 18 (07) : 677 - 696
  • [46] Mechanism of multidrug resistance to chemotherapy mediated by P-glycoprotein (Review)
    Tian, Yichen
    Lei, Yongrong
    Wang, Yani
    Lai, Jiejuan
    Wang, Jianhua
    Xia, Feng
    [J]. INTERNATIONAL JOURNAL OF ONCOLOGY, 2023, 63 (05)
  • [47] Inhibition of human multidrug resistance P-glycoprotein 1 by analogues of a potent δ-opioid antagonist
    Lovekamp, T
    Cooper, PS
    Hardison, J
    Bryant, SD
    Guerrini, R
    Balboni, G
    Salvadori, S
    Lazarus, LH
    [J]. BRAIN RESEARCH, 2001, 902 (01) : 131 - 134
  • [48] Modulation of P-glycoprotein by Stemona alkaloids in human multidrug resistance leukemic cells and structural relationships
    Umsumarng, Sonthaya
    Pitchakarn, Pornsiri
    Yodkeeree, Supachai
    Punfa, Wanisa
    Mapoung, Sariya
    Ramli, Rosdayati Alino
    Pyne, Stephen G.
    Limtrakul, Pornngarm
    [J]. PHYTOMEDICINE, 2017, 34 : 182 - 190
  • [49] Bromocriptine reverses P-glycoprotein-mediated multidrug resistance in tumor cells
    Shiraki, N
    Okamura, K
    Tokunaga, J
    Ohmura, T
    Yasuda, K
    Kawaguchi, T
    Hamada, A
    Nakano, M
    [J]. JAPANESE JOURNAL OF CANCER RESEARCH, 2002, 93 (02): : 209 - 215
  • [50] Modulation of P-glycoprotein function and reversal of multidrug resistance by (-)-epigallocatechin gallate in human cancer cells
    Qian, F
    Wei, DZ
    Zhang, Q
    Yang, SL
    [J]. BIOMEDICINE & PHARMACOTHERAPY, 2005, 59 (03) : 64 - 69