The proteasome inhibitor bortezomib reverses P-glycoprotein-mediated leukemia multi-drug resistance through the NF-κB pathway

H Wang, X Wang, Y Li, A Liao, B Fu… - Die Pharmazie-An …, 2012 - ingentaconnect.com
Multi-drug resistance (MDR) is one of the obstacles for leukemia therapy, the major cause is
an overexpression of P-glycoprotein (P-gp) leading to increased drug efflux. We investigated …

Proteasome inhibitor bortezomib overcomes P‐gp‐mediated multidrug resistance in resistant leukemic cell lines

B Zheng, R Zhou, Y Gong, X Yang… - International journal of …, 2012 - Wiley Online Library
Introduction: To study the effect of bortezomib alone or in combination with daunorubicin
(DNR) on an mdr1 single‐factor drug‐resistant leukemia cell line K562/MDR1, a multifactor …

Bortezomib activity and in vitro interactions with anthracyclines and cytarabine in acute myeloid leukemia cells are independent of multidrug resistance mechanisms …

H Minderman, Y Zhou, KL O'Loughlin… - Cancer chemotherapy and …, 2007 - Springer
Purpose The proteasome inhibitor bortezomib may be effective in combination with
cytarabine and anthracyclines in the treatment of acute myeloid leukemia (AML) by virtue of …

The development of the reversal of the tumor multidrug resistance

C Dai, L FU - Chinese Pharmacological Bulletin, 1986 - pesquisa.bvsalud.org
Multidrug resistance (MDR) of tumor cells has become the main impediment that influence
the curative effect of cancer chemotherapy. Although there are many mechanisms can …

Exploration of Molecular Targets in the Development of New Therapeutics Aimed at Overcoming Multidrug Resistance.

S Nishida, M Tsubaki - … : Journal of the Pharmaceutical Society of …, 2017 - europepmc.org
Multidrug resistance (MDR) in cancer is a major problem in clinical settings: MDR correlates
with a patient's poor prognosis and decreased quality of life. Recently, MDR was found to be …

[HTML][HTML] Modulation of P-glycoprotein expression by triptolide in adriamycin-resistant K562/A02 cells

H Li, L Hui, W Xu, H Shen, Q Chen… - Oncology …, 2012 - spandidos-publications.com
Multidrug resistance is a serious obstacle encountered in leukemia treatment. Previous
studies have found drug resistance in human leukemia is mainly associated with …

NF-kappaB regulating expression of mdr1 gene and P-gp to reverse drug-resistance in leukemic cells

Y Wang, X Liu, HT Zhang, M Yu… - … shi yan xue ye xue za zhi, 2007 - europepmc.org
This study was purposed to investigate whether the mdr1 participates in antiapoptotic
mechanisms of hematologic malignant cells regulated by NF-kappaB and to explore the …

SB203580, a specific inhibitor of p38-MAPK pathway, is a new reversal agent of P-glycoprotein-mediated multidrug resistance

M Barančı́k, V Boháčová, J Kvačkajová… - European journal of …, 2001 - Elsevier
P-glycoprotein (P-gp) is the plasma membrane transport pump responsible for efflux of
chemotherapeutic agents from cells and is one of the systems that secures multidrug …

Multidrug resistance in leukemic cell line K562/A02 induced by doxorubicin.

CZ Yang, FJ Luan, DS Xiong, BR Liu… - Zhongguo yao li xue …, 1995 - europepmc.org
Methods A human leukemic cell line K562/A02 was established by stepwise increase of
concentrations of doxorubicin (Dox) in medium. P-glycoprotein was detected by …

Proteasome inhibitors can alter the signaling pathways and attenuate the P‐glycoprotein‐mediated multidrug resistance

T Fujita, K Washio, D Takabatake… - … journal of cancer, 2005 - Wiley Online Library
Numerous signaling pathways were reported to be involved in the resistance for
conventional cytotoxic drugs, although one of the main reasons is the overexpression of P …