Reversal of P-glycoprotein-mediated multidrug resistance by the novel tetrandrine derivative W6

H Sun, XD Liu, Q Liu, FP Wang, XQ Bao… - Journal of Asian natural …, 2015 - Taylor & Francis
Overexpression of ATP-dependent efflux pump P-glycoprotein (P-gp) is the main cause of
multidrug resistance (MDR) and chemotherapy failure in cancer treatment. Inhibition of P-gp …

The novel bis-benzylisoquinoline PY35 reverses P-glycoprotein-mediated multidrug resistance

Z Cao, M Wright, J Cheng, X Huang… - Oncology …, 2014 - spandidos-publications.com
Multidrug resistance (MDR) to chemotherapeutic drugs is the main cause of chemotherapy
failure in cancer treatment, and it generally results from expression of ATP-dependent efflux …

H1, a novel derivative of tetrandrine reverse P-glycoprotein-mediated multidrug resistance by inhibiting transport function and expression of P-glycoprotein

N Wei, H Sun, F Wang, G Liu - Cancer chemotherapy and pharmacology, 2011 - Springer
Purpose H1 is a novel derivative of tetrandrine (Tet). Here we investigate the ability of H1 to
reverse P-glycoprotein (Pgp)-mediated multidrug resistance (MDR) and its mechanisms …

Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells

Z Cao, D Li, L Liu, P Yang - Oncology Letters, 2018 - spandidos-publications.com
Tetrandrine (Tet) is a potent inhibitor that reverses P‑glycoprotein‑mediated multidrug
resistance (MDR). A number of novel 5‑substituted tetrandrine derivatives were synthesized …

Simplified derivatives of tetrandrine as potent and specific P-gp inhibitors to reverse multidrug resistance in cancer chemotherapy

R Zeng, XM Yang, HW Li, X Li, Y Guan… - Journal of Medicinal …, 2023 - ACS Publications
Targeted inhibition of a drug efflux transporter P-glycoprotein (P-gp) is an important strategy
to reverse multidrug resistance in cancer chemotherapy. In this study, a rationally structural …

HZ08 Reverse P-Glycoprotein Mediated Multidrug Resistance In Vitro and In Vivo

Z Hu, Z Zhou, Y Hu, J Wu, Y Li, W Huang - PLoS One, 2015 - journals.plos.org
Background Multidrug efflux transporter P-glycoprotein (P-gp) is highly expressed on
membrane of tumor cells and is implicated in resistance to tumor chemotherapy. HZ08 is …

A myrsinol diterpene isolated from Euphorbia prolifera reverses multidrug resistance in breast cancer cells

X Chen, X Chen, X Liu, M Wink, Y Ma… - Die Pharmazie-An …, 2016 - ingentaconnect.com
P-glycoprotein (P-gp), a member of ATP-Binding Cassette transporter superfamily, can expel
a variety of anti-cancer drugs so that it impairs the effect of cancer chemotherapy and results …

Pinostrobin and tectochrysin conquer multidrug-resistant cancer cells via inhibiting P-glycoprotein ATPase

IT Wu, CY Kuo, CH Su, YH Lan, CC Hung - Pharmaceuticals, 2023 - mdpi.com
Enhanced drug efflux through ATP-binding cassette transporters, particularly P-glycoprotein
(P-gp), is a key mechanism underlying multidrug resistance (MDR). In the present study, we …

Tetrandrine and fangchinoline, bisbenzylisoquinoline alkaloids from Stephania tetrandra can reverse multidrug resistance by inhibiting P-glycoprotein activity in …

YF Sun, M Wink - Phytomedicine, 2014 - Elsevier
The overexpression of ABC transporters is a common reason for multidrug resistance (MDR)
in cancer cells. In this study, we found that the isoquinoline alkaloids tetrandrine and …

Reversal effect of isotetrandrine, an isoquinoline alkaloid extracted from Caulis Mahoniae, on P-glycoprotein-mediated doxorubicin-resistance in human breast cancer …

TX Wang, XH Yang - Yao xue xue bao= Acta Pharmaceutica Sinica, 2008 - europepmc.org
This study investigated the reversal effect of isotetrandrine, an isoquinoline alkaloid
extracted from Caulis mahoniae, on P-glycoprotein-mediated multidrug resistance in human …