Cinnamylidene ketones as potential modulators of multidrug resistance in mouse lymphoma and human colon cancer cell lines

H Engi, N Gyémánt, T Lóránd, A Lévai, I Ocsovszki… - in vivo, 2006 - iv.iiarjournals.org
The resistance to chemotherapy of cancer cells is mediated by the overexpression of P-
glycoprotein, as an ATP-dependent membrane efflux pump. Two families of compounds …

MDR-reversal activity of chalcones

A Ivanova, D Batovska, H Engi, S Parushev… - in vivo, 2008 - iv.iiarjournals.org
The ability of 11 chalcones with 3, 4, 5-trimethoxy substitution on ring A to inhibit the
transport activity of P-glycoprotein was studied. Flow cytometry was applied in multidrug …

Inhibition of multidrug resistance of cancer cells by natural diterpenes, triterpenes and carotenoids

J Molnár, N Gyémánt, M Tanaka… - Current …, 2006 - ingentaconnect.com
The multidrug resistance (MDR) proteins are member of the ATP-binding cassette
superfamily and are present in a majority of human tumors. Their activity is a crucial factor …

Acridones circumvent P-glycoprotein-associated multidrug resistance (MDR) in cancer cells

VS Gopinath, P Thimmaiah, KN Thimmaiah - Bioorganic & medicinal …, 2008 - Elsevier
Multidrug resistance (MDR) mediated by overexpression of MDR1 P-glycoprotein (P-gp) is
one of the best characterized transporter-mediated barriers to successful chemotherapy in …

Overcoming multidrug resistance (MDR) in cancer in vitro and in vivo by a quinoline derivative

A Ganguly, K Banerjee, P Chakraborty, S Das… - Biomedicine & …, 2011 - Elsevier
Multidrug resistance (MDR) mediated by the over expression of drug efflux protein P-
glycoprotein (P-gp) is one of the major impediments to successful treatment of cancer. P-gp …

Reversal of multidrug resistance by synthetic and natural compounds in drug-resistant MCF-7 cell lines

MD Kars, OD İşeri, U Gunduz, J Molnar - Chemotherapy, 2008 - karger.com
Background: Ineffectiveness of anticancer drugs is frequently observed in cancer
chemotherapy. The resistance of tumor cells to various cytotoxic drugs is defined as …

5-Oxo-hexahydroquinoline derivatives as modulators of P-gp, MRP1 and BCRP transporters to overcome multidrug resistance in cancer cells

S Ranjbar, R Khonkarn, A Moreno… - Toxicology and Applied …, 2019 - Elsevier
Multidrug resistance (MDR) in cancer cells is often associated with overexpression of ATP-
binding cassette (ABC) transporters, including P-glycoprotein (P-gp/ABCB1), multidrug …

[HTML][HTML] Development of a novel quinoline derivative as a P-glycoprotein inhibitor to reverse multidrug resistance in cancer cells

Y Zhou, P Chung, JY Ma, AK Lam, S Law, K Chan… - Biology, 2019 - mdpi.com
Multidrug resistance (MDR) is one of conventional cancer chemotherapy's limitations. Our
group previously synthesized a series of quinoline-based compounds in an attempt to …

[HTML][HTML] Modulators of multidrug resistance: preclinical studies

JM Ford - Hematology/oncology clinics of North America, 1995 - Elsevier
Numerous compounds have been identified that sensitize multidrug-resistant cells to
chemotherapeutic drugs in experimental systems. The mechanism of activity of these …

Tumour-specific cytotoxicity and MDR-reversal activity of dihydropyridines

H Engi, H Sakagami, M Kawase, A Parecha, D Manvar… - in vivo, 2006 - iv.iiarjournals.org
The ability of 41 1, 4-diphenyl-1, 4-dihydropyridine derivatives to inhibit the transport activity
of P-glycoprotein were studied by flow cytometry in a multidrug-resistant human colon …