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
. 2025 Jun 8;42(7):245.
doi: 10.1007/s12032-025-02780-8.

Chloroquine as a potential anticancer agent for triple-negative breast cancer: effects on MDA-MB-231 cells

Affiliations

Chloroquine as a potential anticancer agent for triple-negative breast cancer: effects on MDA-MB-231 cells

Haripriya Dayalan et al. Med Oncol. .

Abstract

Breast cancer is a major cause of mortality among women worldwide, with triple-negative breast cancer (TNBC) presenting a particularly serious clinical challenge due to its low survival rates and high likelihood of recurrence. Despite the availability of several treatment options, more effective and targeted therapies are urgently needed. Chloroquine (CQ), a well-known anti-malarial drug, has recently emerged as a potential anti-cancer agent and chemo sensitizer when combined with other treatments. In this study, we evaluated the anticancer effects of CQ on MDA-MB-231 cells, a human TNBC cell line. Cells were treated with varying concentrations of chloroquine (CQ), and cell viability was assessed using the MTT assay, resulting in an IC₅₀ value of 113 μg/mL with 87.28% inhibition. Additional analyses including DAPI staining flow cytometry for cell cycle analysis, trypan blue exclusion and LDH leakage and scratch wound healing assays were performed to assess cytotoxicity, proliferation, and cell migration. The results demonstrated that CQ significantly reduced cell viability and effectively inhibited the proliferation, migration, and invasion of MDA-MB-231 cells. This novelty of this study was potential of chloroquine as a promising therapeutic agent for the treatment of TNBC.

Keywords: Anti-cancer activity; Breast cancer; Chloroquine; Drug repurposing.

PubMed Disclaimer

Conflict of interest statement

Declarations. Conflict of interest: The authors declared that there is no conflict of interest Ethical approval: Not applicable. Consent to participate: Not applicable. Consent for publication: All the authors agreed to publish the data in this journal.

Similar articles

References

    1. Sriharikrishnaa S, Suresh PS, Prasada KS. An introduction to fundamentals of cancer biology. In: Optical Polarimetric Modalities for Biomedical Research. Cham: Springer International Publishing; 2023. p. 307–30.
    1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA A Cancer J Clin. 2018;68(1):7–30.
    1. Xiong N, Wu H, Yu Z. Advancements and challenges in triple-negative breast cancer: a comprehensive review of therapeutic and diagnostic strategies. Front Oncol. 2024;14:1405491. - PubMed - PMC
    1. Li ZL, Zhang HL, Huang Y, Huang JH, Sun P, Zhou NN, Chen YH, Mai J, Wang Y, Yu Y, Zhou LH. Autophagy deficiency promotes triple-negative breast cancer resistance to T cell-mediated cytotoxicity by blocking tenascin-C degradation. Nat Commun. 2020;11(1):3806. - PubMed - PMC
    1. Kruk J, Aboul-Enein HY. Environmental exposure, and other behavioral risk factors in breast cancer. Curr Cancer Ther Rev. 2006;2(1):3–21.

MeSH terms

LinkOut - more resources