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Book ChapterDOI

Mechanisms of multidrug resistance in cancer.

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TLDR
Identifying genes and mechanisms critical to the development of MDR in vivo and establishing a reliable method for analyzing clinical samples could help to predict theDevelopment of resistance and lead to treatments designed to circumvent it.
Abstract
The development of multidrug resistance (MDR) to chemotherapy remains a major challenge in the treatment of cancer. Resistance exists against every effective anticancer drug and can develop by numerous mechanisms including decreased drug uptake, increased drug efflux, activation of detoxifying systems, activation of DNA repair mechanisms, evasion of drug-induced apoptosis, etc. In the first part of this chapter, we briefly summarize the current knowledge on individual cellular mechanisms responsible for MDR, with a special emphasis on ATP-binding cassette transporters, perhaps the main theme of this textbook. Although extensive work has been done to characterize MDR mechanisms in vitro, the translation of this knowledge to the clinic has not been crowned with success. Therefore, identifying genes and mechanisms critical to the development of MDR in vivo and establishing a reliable method for analyzing clinical samples could help to predict the development of resistance and lead to treatments designed to circumvent it. Our thoughts about translational research needed to achieve significant progress in the understanding of this complex phenomenon are therefore discussed in a third section. The pleotropic response of cancer cells to chemotherapy is summarized in a concluding diagram.

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Journal ArticleDOI

Peroxisome proliferator-activated receptors in regulation of cytochromes P450: new way to overcome multidrug resistance?

TL;DR: It was found that CYP epoxygenases are affected by peroxisome proliferator-activated receptor α (PPARα), and it is assumed that PPARs ligands may regulate CYP2C and CyP2J and in some extent they may contribute to overcoming of MDR in patients with different types of tumours.
Journal ArticleDOI

Overexpression of Human ABCB1 in Cancer Cells Leads to Reduced Activity of GSK461364, a Specific Inhibitor of Polo-like Kinase 1

TL;DR: It is discovered that, by inhibiting the function of ABCB1, the reduced G2/M cell cycle arrest, apoptosis, and sensitivity to GSK461364 treatment in ABCB 1-overexpressing cells can be significantly restored.
Journal ArticleDOI

Sitravatinib Sensitizes ABCB1- and ABCG2-Overexpressing Multidrug-Resistant Cancer Cells to Chemotherapeutic Drugs.

TL;DR: A potential drug repositioning treatment option for multidrug-resistant cancers is revealed by targeting ABCB1 and ABCG2 with sitravatinib by targeting them with a novel multitargeted receptor tyrosine kinase inhibitor.
Journal ArticleDOI

Ancistroyafungines A-D, 5,8'- and 5,1'-coupled naphthylisoquinoline alkaloids from a Congolese Ancistrocladus species, with antiausterity activities against human PANC-1 pancreatic cancer cells.

TL;DR: Four new naphthylisoquinoline alkaloids have been isolated from the stem bark of an as yet unidentified Ancistrocladus liana recently discovered near the village Yafunga, in the North-Central region of the Democratic Republic of the Congo, and display strong preferential cytotoxic activities towards human PANC-1 pancreatic cancer cells in nutrient-deprived medium.
Journal ArticleDOI

Foldamers as Anticancer Therapeutics: Targeting Protein–Protein Interactions and the Cell Membrane

TL;DR: Targeting important protein–protein interactions involved in carcinogenesis or targeting the cell membrane of a cancer cell directly are just two of the ways in which foldamers hold considerable potential in the treatment of cancer.
References
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Journal ArticleDOI

ONCOMINE: A Cancer Microarray Database and Integrated Data-Mining Platform

TL;DR: ONCOMINE is presented, a cancer microarray database and web-based data-mining platform aimed at facilitating discovery from genome-wide expression analyses and novel biomarkers and therapeutic targets are discovered.
Journal ArticleDOI

A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants.

TL;DR: Observations on the molecular basis of pleiotropic drug resistance are interpreted in terms of a model wherein certain surface glycoproteins control drug permeation by modulating the properties of hydrophobic membrane regions.
Journal ArticleDOI

Targeting multidrug resistance in cancer

TL;DR: Various approaches to combating multidrug-resistant cancer are described, including the development of drugs that engage, evade or exploit efflux by ABC transporters.
Journal ArticleDOI

Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line

TL;DR: Reversion to drug sensitivity was associated with loss of gene amplification and a marked decrease in mRNA expression, and the mRNA encodes a member of the ATP-binding cassette transmembrane transporter superfamily.
Journal ArticleDOI

A "Silent" Polymorphism in the MDR1 Gene Changes Substrate Specificity

TL;DR: It is hypothesized that the presence of a rare codon, marked by the synonymous polymorphism, affects the timing of cotranslational folding and insertion of P-gp into the membrane, thereby altering the structure of substrate and inhibitor interaction sites.
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