Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Oct;54(10):1670-1694.
doi: 10.1038/s12276-022-00864-3. Epub 2022 Oct 12.

Molecular targeted therapy for anticancer treatment

Affiliations
Review

Molecular targeted therapy for anticancer treatment

Hye-Young Min et al. Exp Mol Med. 2022 Oct.

Abstract

Since the initial clinical approval in the late 1990s and remarkable anticancer effects for certain types of cancer, molecular targeted therapy utilizing small molecule agents or therapeutic monoclonal antibodies acting as signal transduction inhibitors has served as a fundamental backbone in precision medicine for cancer treatment. These approaches are now used clinically as first-line therapy for various types of human cancers. Compared to conventional chemotherapy, targeted therapeutic agents have efficient anticancer effects with fewer side effects. However, the emergence of drug resistance is a major drawback of molecular targeted therapy, and several strategies have been attempted to improve therapeutic efficacy by overcoming such resistance. Herein, we summarize current knowledge regarding several targeted therapeutic agents, including classification, a brief biology of target kinases, mechanisms of action, examples of clinically used targeted therapy, and perspectives for future development.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Timeline for the approval of selected molecular targeted therapeutic agents.
The first FDA-approved targeted therapeutic agent for each cellular target (denoted in blankets) is indicated in the timeline.
Fig. 2
Fig. 2. Mechanism of the anticancer effect of molecular targeted therapy.
a Schematic diagrams of the main protumor signal transduction pathways and their inhibition by molecular targeted therapeutic agents. b, c Schematic diagrams for antibody-dependent cellular cytotoxicity b and trogoptosis c. See the text and relevant references for details.

Similar articles

Cited by

References

    1. Sung H, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 2021;71:209–249. - PubMed
    1. Ke X, Shen L. Molecular targeted therapy of cancer: the progress and future prospect. Front. Lab. Med. 2017;1:69–75.
    1. Jemal A, et al. Annual report to the nation on the status of cancer, 1975–2005, featuring trends in lung cancer, tobacco use, and tobacco control. J. Natl Cancer Inst. 2008;100:1672–1694. - PMC - PubMed
    1. Saini KS, Twelves C. Determining lines of therapy in patients with solid cancers: a proposed new systematic and comprehensive framework. Br. J. Cancer. 2021;125:155–163. - PMC - PubMed
    1. Usborne CM, Mullard AP. A review of systemic anticancer therapy in disease palliation. Br. Med. Bull. 2017;125:43–53. - PubMed

Publication types

MeSH terms

Substances