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Updated: Jan 21, 2026

Establishment of Gastric Cancer Patient-derived Xenograft Models and Primary Cell Lines
Published on: July 19, 2019
miR-625 reverses multidrug resistance in gastric cancer cells by directly targeting ALDH1A1
Xufei Gong1, Baoli Xu1, Li Zi1
1Department of General Surgery, Linyi People's Hospital, Linyi, Shandong 276002, People's Republic of China.
Abstract:
Background: microRNAs (miRNAs) are emerging as critical regulators of multidrug resistance (MDR) in gastric cancer, a major cause of chemotherapy failure. miR-625 is downregulated in gastric cancer and negatively associated with metastasis. In the current study, we aimed to investigate whether miR-625 regulates MDR in gastric cancer. Methods: The level of miR-625 in gastric cancer cells with or without MDR was quantified by quantitative reverse transcription PCR (qRT-PCR) analysis. The sensitivity of gastric cancer cells to chemotherapeutic agents was assessed by MTT assay. The protein expression was determined by Western blot analysis, and the luciferase reporter assay was applied to confirm miR-625 regulation of the potential target. Results: miR-625 is downregulated in MDR gastric cancer cells compared with chemosensitive counterparts. In addition, miR-625 increases the sensitivity and promotes apoptosis of gastric cancer cells when treated with different chemotherapeutic agents. Moreover, miR-625 directly targets the aldehyde dehydrogenase 1A1 (ALDH1A1), and importantly, the restoration of ALDH1A1 expression rescues miR-625 effects on MDR in gastric cancer cells. Conclusion: miR-625 reverses MDR in gastric cancer cells by targeting ALDH1A1. Hence, our study identifies miR-625 as a novel regulator of MDR in gastric cancer cells, and implicates its potential application for overcoming MDR in gastric cancer chemotherapy.
Insights
MicroRNA-625 (miR-625) reverses multidrug resistance (MDR) in gastric cancer by targeting aldehyde dehydrogenase 1A1 (ALDH1A1). This finding offers potential for overcoming MDR in gastric cancer chemotherapy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) are key regulators of multidrug resistance (MDR) in gastric cancer.
- Gastric cancer MDR is a primary reason for chemotherapy failure.
- miR-625 is downregulated in gastric cancer and linked to metastasis.
Purpose of the Study:
- To investigate the role of miR-625 in regulating MDR in gastric cancer.
- To determine if miR-625 can overcome MDR in gastric cancer cells.
Main Methods:
- Quantitative reverse transcription PCR (qRT-PCR) to measure miR-625 levels.
- MTT assay to assess chemosensitivity.
- Western blot and luciferase reporter assays to identify miR-625 targets.
Main Results:
- miR-625 was significantly downregulated in MDR gastric cancer cells.
- miR-625 increased gastric cancer cell sensitivity to chemotherapeutic agents and promoted apoptosis.
- miR-625 directly targets aldehyde dehydrogenase 1A1 (ALDH1A1); restoring ALDH1A1 reversed miR-625's effects on MDR.
Conclusions:
- miR-625 reverses MDR in gastric cancer by targeting ALDH1A1.
- miR-625 is a novel regulator of MDR in gastric cancer.
- miR-625 holds potential for overcoming MDR in gastric cancer chemotherapy.
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