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Differential expression profile analysis of cisplatin‑regulated miRNAs in a human gastric cancer cell line
Chunlin Yin1, Xianxian Zheng2, Heping Xiang3
1Department of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230022, P.R. China.
Abstract:
Cisplatin, one of the most commonly used drugs in combination chemotherapy, is an effective anti‑tumor agent widely used for diverse tumor types. MicroRNAs (miRNAs/miRs) are involved in the occurrence, development, diagnosis and treatment of cancer. Therefore, the aim of the current study was to explore whether cisplatin exerts anticancer effects by causing differential expression of miRNAs in human gastric cancer cells. The human gastric cancer cell line NCI‑N87 was cultured with a certain dose of cisplatin and high‑throughput sequencing combined with reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR) was performed to detect cisplatin‑regulated miRNAs. miRNAs upregulated and downregulated following cisplatin exposure were analyzed. High‑throughput sequencing revealed 33 upregulated and 16 downregulated miRNAs. A total of five significantly upregulated and five significantly downregulated miRNAs were identified by RT‑qPCR. The expression levels of hsa‑miR‑1246 and hsa‑miR‑892b were consistent with the results obtained from high‑throughput sequencing. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway clustering of cisplatin‑regulated miRNAs revealed that the miRNAs regulated genes involved in several biological processes and signaling pathways. The results obtained in the current study suggested that cisplatin may exert an important anticancer effect in gastric cancer via complex biological processes and signaling pathways.
Insights
Cisplatin, a chemotherapy drug, alters microRNA (miRNA) expression in human gastric cancer cells. These miRNA changes are linked to complex biological processes and signaling pathways, suggesting a key role in cisplatin's anticancer effects.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Cisplatin is a widely used chemotherapy agent effective against various tumors.
- MicroRNAs (miRNAs) play crucial roles in cancer development and treatment.
- Gastric cancer remains a significant health concern, necessitating novel therapeutic strategies.
Purpose of the Study:
- To investigate the differential expression of miRNAs induced by cisplatin in human gastric cancer cells.
- To identify specific miRNAs regulated by cisplatin exposure.
- To explore the biological processes and pathways influenced by cisplatin-regulated miRNAs.
Main Methods:
- Human gastric cancer cell line (NCI-87) treated with cisplatin.
- High-throughput sequencing to identify differentially expressed miRNAs.
- Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) for validation.
Main Results:
- High-throughput sequencing identified 33 upregulated and 16 downregulated miRNAs.
- RT-qPCR confirmed significant changes in five upregulated and five downregulated miRNAs.
- Expression levels of hsa-miR-1246 and hsa-miR-892b were consistent with sequencing data.
- Pathway analysis indicated that cisplatin-regulated miRNAs affect key biological processes and signaling pathways.
Conclusions:
- Cisplatin induces significant differential expression of miRNAs in gastric cancer cells.
- These miRNA alterations are associated with complex biological processes and signaling pathways.
- Cisplatin likely exerts its anticancer effects in gastric cancer through these miRNA-mediated mechanisms.
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