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Updated: Feb 10, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
TRAIL-PEG-Apt-PLGA nanosystem as an aptamer-targeted drug delivery system potential for triple-negative breast cancer
Gulen Melike Demirbolat1, Aslihan Kucuk2, Omer Erdogan3
1Department of Pharmaceutical Technology, Faculty of Pharmacy, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey.
Abstract:
Targeted drug therapy is very important for the treatment of triple-negative breast cancer (TNBC), and the development of carrier systems to deliver apoptosis-inducing proteins such as TRAIL to cells is important in cancer therapy. In this study, a nanosystem formulation (TRAIL-PEG-Apt-PLGA) encapsulating TNBC-targeted aptamer-bound-TRAIL protein was performed and the efficacy of this system was evaluated in a mouse tumor model. The characterization of TRAIL-PEG-Apt-PLGA was confirmed by FTIR, NTA and SEM microscopy. The efficacy of TRAIL-PEG-Apt-PLGA was evaluated by in vitro release assays and interactions with TNBC cells (MDA-MB-231) and healthy breast cells (MCF-10A). TRAIL-PEG-Apt-PLGA was administered intravenously to NOD/SCID gamma mouse breast tumors and evaluated in vivo. Pharmacokinetics, bioavailability testing, histological staining (DR4/DR5, TUNEL, HE staining) and molecular alterations with PCR array were evaluated in tumor tissues. TRAIL-PEG-Apt-PLGA induced apoptosis in both in vivo and in vitro studies. It was found that it regulated cellular responses along with apoptotic mechanisms in cells without developing resistance in suppressing tumor growth by making changes on Atf2, Casp8, Bcl2 and Irf5 genes and proteins. As a result, the biotechnological drug potential of TRAIL was discovered in an aptamer-bound nanosystem for the treatment of triple-negative breast cancer and innovative applications for clinical use.
Insights
This study developed a novel nanosystem (TRAIL-PEG-Apt-PLGA) to deliver TRAIL protein for triple-negative breast cancer (TNBC) treatment. The targeted therapy effectively induced apoptosis and suppressed tumor growth in preclinical models.
Area of Science:
- Biotechnology
- Nanomedicine
- Oncology
Background:
- Triple-negative breast cancer (TNBC) lacks targeted therapies, necessitating innovative treatment strategies.
- Targeted delivery of apoptosis-inducing proteins, like TRAIL, is crucial for effective cancer therapy.
Purpose of the Study:
- To develop and evaluate a novel nanosystem (TRAIL-PEG-Apt-PLGA) for targeted delivery of TRAIL protein to TNBC cells.
- To assess the in vitro and in vivo efficacy of the TRAIL-PEG-Apt-PLGA system in a TNBC mouse model.
Main Methods:
- Characterization of the TRAIL-PEG-Apt-PLGA nanosystem using FTIR, NTA, and SEM.
- In vitro release assays and cell interaction studies with TNBC (MDA-MB-231) and healthy breast cells (MCF-10A).
- In vivo evaluation in a mouse tumor model, including pharmacokinetics, bioavailability, histological staining, and PCR array analysis.
Main Results:
- TRAIL-PEG-Apt-PLGA demonstrated successful encapsulation and targeted delivery of TRAIL.
- The nanosystem effectively induced apoptosis in both in vitro and in vivo TNBC models.
- Treatment suppressed tumor growth by modulating key genes (Atf2, Casp8, Bcl2, Irf5) without inducing resistance.
Conclusions:
- The aptamer-bound TRAIL nanosystem (TRAIL-PEG-Apt-PLGA) shows significant potential as a biotechnological drug for TNBC treatment.
- This targeted nanodelivery system offers innovative therapeutic applications for clinical use in triple-negative breast cancer.
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