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Updated: Feb 5, 2026

Aptamer-Based Target Detection Facilitated by a 3-Stage G-Quadruplex Isothermal Exponential Amplification Reaction
Published on: October 6, 2022
Gemcitabine-Incorporated G-Quadruplex Aptamer for Targeted Drug Delivery into Pancreas Cancer
Jun Young Park1, Ye Lim Cho2, Ju Ri Chae2
1Department of Nuclear Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea; Department of Anatomy, Yonsei University Wonju College of Medicine, Wonju, Korea.
Abstract:
Gemcitabine has been considered a first-line chemotherapy agent for the treatment of pancreatic cancer. However, the initial response rate of gemcitabine is low and chemoresistance occurs frequently. Aptamers can be effectively internalized into cancer cells via binding to target molecules with high affinity and specificity. In the current study, we constructed an aptamer-based gemcitabine delivery system, APTA-12, and assessed its therapeutic effects on pancreatic cancer cells in vitro and in vivo. APTA-12 was effective in vitro and in vivo in pancreatic cancer cells with high expression of nucleolin. The results of in vitro cytotoxicity assays indicated that APTA-12 inhibited the growth of pancreatic cancer cell lines. In vivo evaluation showed that APTA-12 effectively inhibited the growth of pancreatic cancer in Capan-1 tumor-bearing mice compared to mice that received gemcitabine alone or vehicle. These results suggest that the gemcitabine-incorporated APTA-12 aptamer may be a promising targeted therapeutic strategy for pancreatic cancer.
Insights
A novel aptamer-based gemcitabine delivery system, APTA-12, shows promise for pancreatic cancer treatment. This targeted therapy effectively inhibited cancer cell growth in vitro and in vivo, overcoming gemcitabine resistance.
Area of Science:
- Oncology
- Biotechnology
- Drug Delivery
Background:
- Gemcitabine is a first-line chemotherapy for pancreatic cancer but suffers from low response rates and frequent chemoresistance.
- Aptamers offer targeted delivery of therapeutics into cancer cells due to their high affinity and specificity.
Purpose of the Study:
- To construct and evaluate an aptamer-based gemcitabine delivery system (APTA-12) for pancreatic cancer therapy.
- To assess the in vitro and in vivo therapeutic efficacy of APTA-12 in pancreatic cancer models.
Main Methods:
- Construction of an aptamer-conjugated gemcitabine delivery system, APTA-12.
- In vitro cytotoxicity assays on pancreatic cancer cell lines.
- In vivo efficacy studies using Capan-1 tumor-bearing mice.
Main Results:
- APTA-12 demonstrated significant cytotoxicity against pancreatic cancer cell lines in vitro.
- In vivo studies showed APTA-12 effectively inhibited tumor growth in mice compared to gemcitabine alone.
- Therapeutic effects were observed in pancreatic cancer cells with high nucleolin expression.
Conclusions:
- The gemcitabine-incorporated APTA-12 aptamer system is a potential targeted therapeutic strategy for pancreatic cancer.
- APTA-12 may overcome gemcitabine resistance and improve treatment outcomes for pancreatic cancer patients.
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