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
. 2025;25(6):555-573.
doi: 10.2174/0115680096289260240311062343.

Clinical Progress of Targeted Therapy for Breast Cancer: A Comprehensive Review

Affiliations
Review

Clinical Progress of Targeted Therapy for Breast Cancer: A Comprehensive Review

Abhijit Debnath et al. Curr Cancer Drug Targets. 2025.

Abstract

The discovery of effective breast cancer therapy is both urgent and daunting, beset by a myriad of challenges that range from the disease's inherent heterogeneity to its complex molecular underpinnings. Drug resistance, the intricacies of the tumor microenvironment, and patient-specific variables further complicate this landscape. The stakes are even higher when dealing with subtypes like triple-negative breast cancer, which eludes targeted hormonal therapies due to its lack of estrogen, progesterone, and HER2 receptors. Strategies to overcome such challenges include combinations of drugs and identifying new drug targets. Developing new drugs based on such targets could be a better solution than relying on costly immunotherapy or combinational therapies. In this review, we have endeavored to comprehensively examine the proven therapeutic drug targets associated with breast cancer and elucidate their respective molecular mechanisms and current clinical status. This study aims to facilitate researchers in conducting a comparative analysis of different targets to select single and multi-targeted drug discovery approaches for breast cancer.

Keywords: Breast cancer; FDA-approved breast cancer drugs; breast cancer drug discovery; breast cancer drug targets; drug targets for breast cancer.; molecular mechanisms of cancer; triple-negative breast cancer.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Anandasabapathy S.; Asirwa C.; Grover S.; Mungo C.; Cancer burden in low-income and middle-income countries. Nat Rev Cancer 2024,24(3),167-170 - DOI - PubMed
    1. Brody J.G.; Rudel R.A.; Michels K.B.; Moysich K.B.; Bernstein L.; Attfield K.R.; Gray S.; Environmental pollutants, diet, physical activity, body size, and breast cancer. Cancer 2007,109(S12),2627-2634 - DOI - PubMed
    1. Dent S.F.; The role of VEGF in triple-negative breast cancer: Where do we go from here? Ann Oncol 2009,20(10),1615-1617 - DOI - PubMed
    1. Hsu J.L.; Hung M.C.; The role of HER2, EGFR, and other receptor tyrosine kinases in breast cancer. Cancer Metastasis Rev 2016,35(4),575-588 - DOI - PubMed
    1. Wesolowski R.; Ramaswamy B.; Gene expression profiling: Changing face of breast cancer classification and management. Gene Expr 2011,15(3),105-115 - DOI - PubMed

MeSH terms

Substances