Format

Send to

Choose Destination
Expert Opin Drug Metab Toxicol. 2015 May;11(5):703-17. doi: 10.1517/17425255.2015.1006626. Epub 2015 Jan 29.

Physicochemical properties of novel protein kinase inhibitors in relation to their substrate specificity for drug transporters.

Author information

1
VU University Medical Center, Department of Medical Oncology , PO Box 7057, 1007 MB Amsterdam , The Netherlands.

Abstract

INTRODUCTION:

Small molecule tyrosine and serine-threonine kinase inhibitors (TKIs and STKIs) are emerging drugs that interfere with downstream signaling pathways involved in cancer proliferation, invasion, metastasis and angiogenesis. The understanding of their pharmacokinetics, the identification of their transporters and the modulating activity exerted on transporters is pivotal to predict therapy efficacy and to avoid unwarranted drug treatment combinations.

AREAS COVERED:

Experimental or in silico data were collected and summarized on TKIs and STKIs physico-chemical properties, which influence their transport, metabolism and efficacy, and TKIs and STKIs as influx transporter substrates and inhibitors. In addition, the uptake by tumor cell influx transporters and some factors in the tumor microenvironment affecting the uptake of TKIs and STKIs by cancer cells are briefly covered.

EXPERT OPINION:

Membrane transporters play an important role in the pharmacokinetics and hence the efficacy of anticancer drugs, including TKIs and STKIs. These drugs are substrates and inhibitors of various transporters. Drug resistance may be bypassed not only by identifying the proper transporter but also by selective combinations, which may either downregulate or increase transporter activity. However, care has to be taken because this profile might be disease, drug and patient specific.

KEYWORDS:

efflux transporters; influx transporters; physicochemical properties; serine-threonine kinase inhibitors; tyrosine kinase inhibitors

PMID:
25633410
DOI:
10.1517/17425255.2015.1006626
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Taylor & Francis
Loading ...
Support Center