Novel Aptamer-Drug Conjugate for Targeted Therapy in Triple-Negative Breast Cancer

Triple-negative breast cancer (TNBC) is a highly aggressive malignancy lacking targeted therapeutic modalities. Aptamers are promising targeting agents with high specificity and affinity. In this study, we identified a chemically modified nucleic acid aptamer (AptT1) that specifically recognized and internalized into TNBC cells. Mechanistic studies revealed that ANXA2 was an essential protein in facilitating AptT1 internalization <i>via</i> clathrin-mediated endocytosis. Furthermore, we constructed an aptamer-drug conjugate (ApDC) to selectively deliver a cytotoxic agent (SN38) to TNBC cells and demonstrated significant efficacy and safety in a TNBC xenograft model. These findings suggest that AptT1-based ApDC holds great potential as an innovative targeted strategy for TNBC.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-07-21
DOI
https://doi.org/10.1021/acs.jmedchem.5c00492
Citations
1
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
0.81
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article

Novel Aptamer-Drug Conjugate for Targeted Therapy in Triple-Negative Breast Cancer

Jingtong Xu, Xiaoxiang Guan, Fulong Wang, Hanyang Yu et al.
1 citations
Journal of Medicinal Chemistry
Advanced biosensing and bioanalysis techniques
0.81
article

Novel Aptamer-Drug Conjugate for Targeted Therapy in Triple-Negative Breast Cancer

Jingtong Xu, Xiaoxiang Guan, Fulong Wang, Hanyang Yu, Ke Wang, Feng Xu, Feng Han
article en
1 citations

Abstract

Triple-negative breast cancer (TNBC) is a highly aggressive malignancy lacking targeted therapeutic modalities. Aptamers are promising targeting agents with high specificity and affinity. In this study, we identified a chemically modified nucleic acid aptamer (AptT1) that specifically recognized and internalized into TNBC cells. Mechanistic studies revealed that ANXA2 was an essential protein in facilitating AptT1 internalization <i>via</i> clathrin-mediated endocytosis. Furthermore, we constructed an aptamer-drug conjugate (ApDC) to selectively deliver a cytotoxic agent (SN38) to TNBC cells and demonstrated significant efficacy and safety in a TNBC xenograft model. These findings suggest that AptT1-based ApDC holds great potential as an innovative targeted strategy for TNBC.

Journal of Medicinal ChemistryVol. 68(19)
Center for Personalized Cancer Treatment (NL), Jiangsu Province Hospital (CN), State Key Laboratory of Chemical Engineering (CN), Nanjing Medical University (CN), Nanjing University (CN)
Good health and well-being
Openalex Percentile: Top 26%
Advanced biosensing and bioanalysis techniques
0.81
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