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[Arginine-glycine-aspartic polypeptide mediated truncated tissue factor therapy for colorectal carcinoma]
Zheng-jie Huang1, Qi Luo, Jiang-hua Yan
1Department of General Surgery, Zhongshan Hospital Affiliated to Xiamen University, Xiamen, China.
Objective:
To explore the therapy effects of (arginine-glycine-aspartic, RGD)(3)-truncated tissue factor (tTF) fusion protein on colorectal carcinoma in mice.
Methods:
The (RGD)(3)-tTF fusion gene, constructed with tTF and three series-wound peptides RGD, was expressed in Escherichia coli BL21 (DE(3)). The fusion protein was purified through Nickel affinity chromatography column. The coagulation activity of the (RGD)(3)-tTF fusion protein was detected by clotting assay in vitro. Mice colorectal cancer cells line CT26 were inoculated subcutaneously into mice to establish colorectal cancer model. Four mice were randomly divided into two groups to be injected with the (RGD)(3)-tTF or tTF fusion protein labeled with rhodamine B isothiocyanate (RBITC) at a single dose of 50 microg respectively. The location of the (RGD)(3)-tTF fusion protein in the colorectal carcinoma bearing mice tissue was analyzed by using in vivo optical imaging one hour after the injection and confocal microscopy twenty-four hours after the injection. Fifteen mice bearing colorectal carcinoma were randomly divided into three groups for injection with the (RGD)(3)-tTF, tTF fusion protein or phosphate buffered saline (PBS) at a single dose of 50 microg respectively. The tumor size was measured daily to calculate the tumor volume. Five days after the injection, the mice were killed to harvest tumor tissues, hearts, livers, spleens, lung, kidneys and brains to observe valid thrombogenesis and tumor necrosis.
Results:
With the concentration of the (RGD)(3)-tTF fusion protein increased, the clotting time was shorten correspondingly under the conditions of Ca(2+), and the clotting time was (8.6 +/- 0.2) min when the concentration was 6 micromol/L, and it was >30 min in the group of 0 micromol/L (P < 0.05). The coagulation activity of (RGD)(3)-tTF and tTF fusion protein was alike (F = 0.09, P > 0.05). The in vivo optical imaging and confocal microscopy analyses showed that RBITC fluorescence labeling (RGD)(3)-tTF fusion protein was assembled in the tumor vasculature. On the first, third, fifth day after injection, the tumor volume of (RGD)(3)-tTF fusion protein group was (120.8 +/- 4.8) mm(3), (93.8 +/- 3.4) mm(3), (132.2 +/- 7.7) mm(3) respectively, which was significantly smaller than that of the tTF group [(181.4 +/- 13.8) mm(3), (333.0 +/- 32.0) mm(3), (514.0 +/- 11.5) mm(3)] and PBS group [(182.6 +/- 11.5) mm(3), (332.8 +/- 21.0) mm(3), (524.2 +/- 16.7) mm(3)] (both P < 0.05). However, there was no significant difference in the tumor volume between the latter two groups (P > 0.05).
Conclusion:
The (RGD)(3)-tTF fusion protein is capable of targeting to tumor vasculature and inducing thrombogenesis for suppressing the tumor growth in the colorectal carcinoma mice model, and it's expected to be a new therapy for colorectal cancer.
Insights
The (arginine-glycine-aspartic, RGD)(3)-truncated tissue factor (tTF) fusion protein targets tumor vasculature, inducing thrombogenesis to suppress colorectal cancer growth in mice. This novel fusion protein shows promise as a new colorectal cancer therapy.
Area of Science:
- Biochemistry and Molecular Biology
- Oncology
- Biotechnology
Background:
- Colorectal carcinoma remains a significant global health challenge.
- Targeted therapies are crucial for improving treatment efficacy and reducing side effects.
- Truncated tissue factor (tTF) has potential in cancer therapy through thrombogenesis.
Purpose of the Study:
- To evaluate the therapeutic effects of a novel (arginine-glycine-aspartic, RGD)(3)-truncated tissue factor (tTF) fusion protein.
- To investigate the targeting capability and anti-tumor activity of (RGD)(3)-tTF in a murine colorectal cancer model.
Main Methods:
- The (RGD)(3)-tTF fusion gene was expressed in E. coli and purified.
- Coagulation activity was assessed using in vitro clotting assays.
- A colorectal cancer model was established in mice; tumor targeting was visualized using RBITC labeling, in vivo imaging, and confocal microscopy. Tumor growth inhibition was measured after systemic administration of (RGD)(3)-tTF, tTF, or PBS.
Main Results:
- The (RGD)(3)-tTF fusion protein demonstrated dose-dependent procoagulant activity, similar to tTF.
- In vivo imaging confirmed that (RGD)(3)-tTF accumulated in tumor vasculature.
- Treatment with (RGD)(3)-tTF significantly suppressed tumor volume compared to tTF or PBS controls (P < 0.05).
Conclusions:
- The (RGD)(3)-tTF fusion protein effectively targets tumor vasculature and induces thrombogenesis.
- This targeted thrombogenesis leads to significant suppression of colorectal tumor growth in mice.
- (RGD)(3)-tTF represents a promising novel therapeutic strategy for colorectal cancer.
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