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Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
Improving Targeted Delivery and Antitumor Efficacy with Engineered Tumor Necrosis Factor-Related Apoptosis
Xiaoyuan Yang1, Xuelin Xia1, Xiao-Xia Xia2
1School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, People's Republic of China.
Abstract:
Tumor necrosis factor-related apoptosis ligand (TRAIL) is a promising protein candidate for selective apoptosis of a variety of cancer cells. However, the short half-life and a lack of targeted delivery are major obstacles for its application in cancer therapy. Here, we propose a simple strategy to solve the targeting problem by genetically fusing an anti-HER2 affibody to the C-terminus of the TRAIL. The fusion protein TRAIL-affibody was produced as a soluble form with high yield in recombinant Escherichia coli. In vitro studies proved that the affibody domain promoted the cellular uptake of the fusion protein in the HER2 overexpressed SKOV-3 cells and improved its apoptosis-inducing ability. In addition, the fusion protein exhibited higher accumulation at the tumor site and greater antitumor effect than those of TRAIL in vivo, indicating that the affibody promoted the tumor homing of the TRAIL and then improved the therapeutic efficacy. Importantly, repeated injection of high-dose TRAIL-affibody showed no obvious toxicity in mice. These results demonstrated that the engineered TRAIL-affibody is promising to be a highly tumor-specific and targeted cancer therapeutic agent.
Insights
Engineered TRAIL-affibody fusion protein targets HER2-overexpressing cancer cells. This targeted therapy enhances apoptosis and antitumor effects with no observed toxicity, offering a promising cancer treatment.
Area of Science:
- Biotechnology
- Molecular Biology
- Oncology
Background:
- Tumor necrosis factor-related apoptosis ligand (TRAIL) shows potential for cancer therapy due to selective apoptosis induction.
- Short half-life and lack of targeted delivery limit TRAIL's clinical application.
Purpose of the Study:
- To develop a targeted cancer therapeutic by fusing TRAIL with an anti-HER2 affibody.
- To evaluate the efficacy and safety of the TRAIL-affibody fusion protein.
Main Methods:
- Genetic fusion of anti-HER2 affibody to TRAIL C-terminus.
- Recombinant expression of TRAIL-affibody in Escherichia coli.
- In vitro and in vivo evaluation of cellular uptake, apoptosis induction, tumor accumulation, and antitumor activity.
Main Results:
- TRAIL-affibody was produced in high yield as a soluble protein.
- Affibody enhanced cellular uptake and apoptosis in HER2-overexpressing cells.
- Fusion protein showed improved tumor homing, increased antitumor efficacy, and no significant toxicity in mice.
Conclusions:
- The engineered TRAIL-affibody demonstrates enhanced tumor targeting and therapeutic efficacy.
- This fusion protein represents a promising, tumor-specific, and targeted cancer therapeutic agent.
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