Tyrosine kinase inhibitors enhanced the efficacy of conventional chemotherapeutic agent in multidrug resistant cancer cells
S Wu, L Fu - Molecular cancer, 2018 - Springer
Multidrug resistance (MDR) triggered by ATP binding cassette (ABC) transporter such as
ABCB1, ABCC1, ABCG2 limited successful cancer chemotherapy. Unfortunately, no …
ABCB1, ABCC1, ABCG2 limited successful cancer chemotherapy. Unfortunately, no …
Tyrosine kinase inhibitors as modulators of ABC transporter-mediated drug resistance
S Shukla, ZS Chen, SV Ambudkar - Drug resistance updates, 2012 - Elsevier
Tyrosine kinases (TKs) are involved in key signaling events/pathways that regulate cancer
cell proliferation, apoptosis, angiogenesis and metastasis. Deregulated activity of TKs has …
cell proliferation, apoptosis, angiogenesis and metastasis. Deregulated activity of TKs has …
Nilotinib (AMN107, Tasigna®) reverses multidrug resistance by inhibiting the activity of the ABCB1/Pgp and ABCG2/BCRP/MXR transporters
Nilotinib, a BCR-Abl tyrosine kinase inhibitor (TKI), was developed to surmount resistance or
intolerance to imatinib in patients with Philadelphia positive chronic myelogenous leukemia …
intolerance to imatinib in patients with Philadelphia positive chronic myelogenous leukemia …
Sildenafil reverses ABCB1-and ABCG2-mediated chemotherapeutic drug resistance
Sildenafil is a potent and selective inhibitor of the type 5 cGMP (cyclic guanosine 3′, 5′-
monophosphate)-specific phosphodiesterase that is used clinically to treat erectile …
monophosphate)-specific phosphodiesterase that is used clinically to treat erectile …
Nilotinib potentiates anticancer drug sensitivity in murine ABCB1-, ABCG2-, and ABCC10-multidrug resistance xenograft models
A panel of clinically used tyrosine kinase inhibitors were compared and nilotinib was found
to most potently sensitize specific anticancer agents by blocking the functions of ABCB1/P …
to most potently sensitize specific anticancer agents by blocking the functions of ABCB1/P …
Carvacrol alleviates prostate cancer cell proliferation, migration, and invasion through regulation of PI3K/Akt and MAPK signaling pathways
Y Luo, JY Wu, MH Lu, Z Shi, N Na… - Oxidative medicine and …, 2016 - Wiley Online Library
TRPM7 is a potential therapeutic target for treatment of prostate cancer. In this study, we
investigated the effects of nonselective TRPM7 inhibitor carvacrol on cell proliferation …
investigated the effects of nonselective TRPM7 inhibitor carvacrol on cell proliferation …
[HTML][HTML] Sildenafil inhibits the growth of human colorectal cancer in vitro and in vivo
XL Mei, Y Yang, YJ Zhang, Y Li, JM Zhao… - American journal of …, 2015 - ncbi.nlm.nih.gov
Colorectal cancer is the third most common human cancer with frequent overexpression of
the cGMP-specific phosphodiesterase 5 (PDE5). In the present study, we investigated that …
the cGMP-specific phosphodiesterase 5 (PDE5). In the present study, we investigated that …
ABCG2/BCRP: specific and nonspecific modulators
D Peña‐Solórzano, SA Stark, B König… - Medicinal research …, 2017 - Wiley Online Library
Multidrug resistance (MDR) in cancer cells is the development of resistance to a variety of
structurally and functionally nonrelated anticancer drugs. This phenomenon has become a …
structurally and functionally nonrelated anticancer drugs. This phenomenon has become a …
Combination of HGF/MET-targeting agents and other therapeutic strategies in cancer
MET receptor has emerged as a druggable target across several human cancers. Agents
targeting MET and its ligand hepatocyte growth factor (HGF) including small molecules such …
targeting MET and its ligand hepatocyte growth factor (HGF) including small molecules such …
ABC transporter inhibitors in reversing multidrug resistance to chemotherapy
H Cui, A J. Zhang, M Chen, J J. Liu - Current drug targets, 2015 - benthamdirect.com
The superfamily of human ATP-binding cassette (ABC) transporters comprises seven
subfamilies (ABCA to G) with 48 members. In addition to their profound physiological and …
subfamilies (ABCA to G) with 48 members. In addition to their profound physiological and …