Back to Search Start Over

Screening and identification of molecular targets for cancer therapy.

Authors :
Abdelmoez A
Coraça-Huber DC
Thurner GC
Debbage P
Lukas P
Skvortsov S
Skvortsova II
Source :
Cancer letters [Cancer Lett] 2017 Feb 28; Vol. 387, pp. 3-9. Date of Electronic Publication: 2016 Mar 08.
Publication Year :
2017

Abstract

In recent decades, targeted therapeutics have significantly improved therapy results in patients with malignant tumors of different origins. However, malignant diseases characterized by aggressiveness and increased capacity for metastatic spread still require basic researchers and clinicians to direct enormous efforts toward the development of novel therapeutic targets. Potential targets should be selected with the clinical endpoint in view; targeted therapeutics can be developed: for use in combination with currently existing therapeutic approaches in order to improve their efficacy; to overcome the treatment resistance of tumor cells and thus protect the patient from recurrence; to repress molecular mechanisms related to immune escape of cancer cells; and to combat the metastatic dissemination of carcinoma cells. Taking into account the specific clinical aim that should be achieved, different strategies and techniques can be proposed to identify the most promising candidate molecules for further development as therapeutic targets. Since cellular membranes contain a large number of druggable molecules, evaluation of the membrane protein profiles of carcinoma cells having different properties can provide a basis for further development of therapeutic targets. This review considers how cellular membranes obtained from different pre-clinical and clinical samples can be used in screening and to identify targets for cancer therapy.<br /> (Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1872-7980
Volume :
387
Database :
MEDLINE
Journal :
Cancer letters
Publication Type :
Academic Journal
Accession number :
26968248
Full Text :
https://doi.org/10.1016/j.canlet.2016.03.002