Evolution of Molecular Targeted Cancer Therapy: Mechanisms of Drug Resistance and Novel Opportunities Identified by CRISPR-Cas9 Screening

Molecular targeted therapy has revolutionized the landscape of cancer treatment due to better therapeutic responses and less systemic toxicity. However, therapeutic resistance is a major challenge in clinical settings that hinders continuous clinical benefits for cancer patients. In this regard, unr...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in oncology Vol. 12; p. 755053
Main Authors Hou, Jue, He, Zongsheng, Liu, Tian, Chen, Dongfeng, Wang, Bin, Wen, Qinglian, Zheng, Xi
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 17.03.2022
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Molecular targeted therapy has revolutionized the landscape of cancer treatment due to better therapeutic responses and less systemic toxicity. However, therapeutic resistance is a major challenge in clinical settings that hinders continuous clinical benefits for cancer patients. In this regard, unraveling the mechanisms of drug resistance may identify new druggable genetic alterations for molecularly targeted therapies, thus contributing to improved therapeutic efficacies. The recent rapid development of novel methodologies including CRISPR-Cas9 screening technology and patient-derived models provides powerful tools to dissect the underlying mechanisms of resistance to targeted cancer therapies. In this review, we updated therapeutic targets undergoing preclinical and clinical evaluation for various cancer types. More importantly, we provided comprehensive elaboration of high throughput CRISPR-Cas9 screening in deciphering potential mechanisms of unresponsiveness to molecularly targeted therapies, which will shed light on the discovery of novel opportunities for designing next-generation anti-cancer drugs.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
Edited by: Jing Hong Wang, University of Pittsburgh Medical Center, United States
This article was submitted to Molecular and Cellular Oncology, a section of the journal Frontiers in Oncology
Reviewed by: Vincenzo Di Donato, ZeClinics SL, Spain; Bernhard Schmierer, Karolinska Institutet (KI), Sweden
These authors share first authorship
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2022.755053