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A DNA aptamer with high affinity and specificity for molecular recognition and targeting therapy of gastric cancer
Hong-Yong Cao, Ai-Hua Yuan1, Wei Chen
1Department of General Surgery, Nanjing Hospital Affiliated to Nanjing Medical University, Nanjing, P, R, China. njmuyah@126.com.
Background:
Aptamers have emerged as excellent molecular probes for cancer diagnosis and therapy. The aim of the current study was to determine the feasibility of using DNA aptamer cy-apt 20 developed by live cell-SELEX for detecting and targeting gastric cancer.
Methods:
The specificity, sensitivity and biostability of cy-apt 20 in detecting gastric cancer were assessed by binding assay, cell fluorescence imaging, and in vivo tumor imaging in animal model in comparison with non-gastric cancers.
Results:
Flow cytometric analysis showed that cy-apt 20 had higher than 78% of maximal binding rate to gastric cancer cells, much higher than that of non-gastric cancer cells. Cell fluorescence imaging and in vivo tumor imaging showed that the targeting recognition could be visualized by using minimal dose of fluorochrome labeled cy-apt 20. Meanwhile, strong fluorescence signals were detected and lasted for a period of time longer than 50 min in vitro and 240 min in vivo. The fluorescence intensities of gastric cancer were about seven folds in vitro and five folds of that of non-gastric cancers in vivo.
Conclusion:
Our study demonstrated that cy-apt 20 was an excellent molecular probe with high specificity and sensitivity and a certain degree of biostability for molecular recognition and targeting therapy of gastric cancer.
Insights
DNA aptamer cy-apt 20 shows high specificity and sensitivity for detecting gastric cancer. This molecular probe is effective for both diagnosis and targeted therapy, demonstrating significant potential in preclinical studies.
Area of Science:
- Biotechnology
- Molecular Biology
- Oncology
Background:
- Aptamers are valuable molecular probes for cancer diagnosis and therapy.
- DNA aptamer cy-apt 20 was developed using live cell-SELEX.
Purpose of the Study:
- To evaluate the feasibility of using DNA aptamer cy-apt 20 for gastric cancer detection and targeting.
- To assess the specificity, sensitivity, and biostability of cy-apt 20 against gastric cancer.
Main Methods:
- Binding assays were performed to determine specificity.
- Cell fluorescence imaging and in vivo tumor imaging were used to visualize targeting.
- Comparison with non-gastric cancers was conducted.
Main Results:
- Cy-apt 20 exhibited a maximal binding rate over 78% to gastric cancer cells, significantly higher than non-gastric cancer cells.
- Targeting recognition was visualized using minimal doses of fluorochrome-labeled cy-apt 20.
- Gastric cancer showed approximately 7-fold higher fluorescence intensity in vitro and 5-fold higher in vivo compared to non-gastric cancers, with signals lasting over 50 min in vitro and 240 min in vivo.
Conclusions:
- Cy-apt 20 is a highly specific and sensitive molecular probe for gastric cancer.
- The aptamer demonstrates good biostability, suitable for molecular recognition and targeted therapy.
- Cy-apt 20 shows promise as a diagnostic and therapeutic agent for gastric cancer.
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