Mammalian drug efflux transporters of the ATP binding cassette (ABC) family in multidrug resistance: A review of the past decade

Z Chen, T Shi, L Zhang, P Zhu, M Deng, C Huang, T Hu… - Cancer letters, 2016 - Elsevier
Multidrug resistance (MDR) is a serious phenomenon employed by cancer cells which
hampers the success of cancer pharmacotherapy. One of the common mechanisms of MDR …

Improvement of conventional anti-cancer drugs as new tools against multidrug resistant tumors

S Dallavalle, V Dobričić, L Lazzarato, E Gazzano… - Drug Resistance …, 2020 - Elsevier
Multidrug resistance (MDR) is the dominant cause of the failure of cancer chemotherapy.
The design of antitumor drugs that are able to evade MDR is rapidly evolving, showing that …

The National Cancer Institute ALMANAC: a comprehensive screening resource for the detection of anticancer drug pairs with enhanced therapeutic activity

SL Holbeck, R Camalier, JA Crowell… - Cancer research, 2017 - AACR
To date, over 100 small-molecule oncology drugs have been approved by the FDA.
Because of the inherent heterogeneity of tumors, these small molecules are often …

Nilotinib potentiates anticancer drug sensitivity in murine ABCB1-, ABCG2-, and ABCC10-multidrug resistance xenograft models

AK Tiwari, K Sodani, C Dai, AH Abuznait, S Singh… - Cancer letters, 2013 - Elsevier
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 …

Dual inhibitors as a new challenge for cancer multidrug resistance treatment

T Stanković, J Dinić, A Podolski-Renić… - Current Medicinal …, 2019 - ingentaconnect.com
Background: Dual-targeting in cancer treatment by a single drug is an unconventional
approach in relation to drug combinations. The rationale for the development of …

ABC transporters in multi-drug resistance and ADME-Tox of small molecule tyrosine kinase inhibitors

J Deng, J Shao, JS Markowitz, G An - Pharmaceutical research, 2014 - Springer
The past decade has seen tremendous efforts in the research and development of new
chemotherapeutic drugs using target-based approaches. These efforts have led to the …

Pharmacokinetic drug‐drug interactions of tyrosine kinase inhibitors: A focus on cytochrome P450, transporters, and acid suppression therapy

C Gay, D Toulet, P Le Corre - Hematological oncology, 2017 - Wiley Online Library
The extensive use of tyrosine kinase inhibitors (TKI's) in hematology and oncology has
shown that these drugs have a significant potential for drug‐drug interactions. Since these …

[HTML][HTML] The biology and treatment of leiomyosarcomas

WGJ Kerrison, K Thway, RL Jones… - Critical Reviews in …, 2023 - Elsevier
Leiomyosarcoma (LMS) is a soft tissue sarcoma of smooth muscle origin that can arise in
multiple anatomical sites and is broadly classified as extra-uterine LMS or uterine LMS …

Small molecule kinase inhibitors block the ZAK-dependent inflammatory effects of doxorubicin

J Wong, LB Smith, EA Magun, T Engstrom… - Cancer biology & …, 2013 - Taylor & Francis
The adverse side effects of doxorubicin, including cardiotoxicity and cancer treatment-
related fatigue, have been associated with inflammatory cytokines, many of which are …

p38MAPK and chemotherapy: we always need to hear both sides of the story

J García-Cano, O Roche, FJ Cimas… - Frontiers in cell and …, 2016 - frontiersin.org
The p38MAPK signaling pathway was initially described as a stress response mechanism.
In fact, during previous decades, it was considered a pathway with little interest in oncology …