Metformin up-regulated miR-107 expression and enhanced the inhibitory effect of miR-107 on gastric cancer growth

Yongyi Chen1,2,3, Wangang Gong1,2,3, Yun Zhou1,2,3

  • 1Institute of Cancer Research and Basic Medical Sciences of Chinese Academy of Sciences, Hangzhou 310022, China.

Insights

Metformin enhances anti-cancer effects in gastric cancer (GC) by up-regulating miR-107. This microRNA (miRNA) targets MAPK8, offering a new therapeutic strategy for GC treatment.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Gastric cancer (GC) is a leading cause of cancer-related death globally.
  • Metformin shows anti-cancer properties by regulating microRNAs (miRNAs).
  • The specific miRNAs influenced by metformin in GC remain largely unidentified.

Purpose of the Study:

  • To identify microRNAs regulated by metformin in gastric cancer cells.
  • To investigate the role of miR-107 in metformin's anti-cancer effects on GC.
  • To explore the molecular mechanisms linking metformin, miR-107, and GC progression.

Main Methods:

  • In vitro cell culture using SGC-7901 and MGC803 gastric cancer cell lines.
  • Real-time reverse transcription polymerase chain reaction (RT-PCR) to quantify miR-107 expression.
  • Bioinformatics analysis to identify potential molecular targets of metformin and miR-107.

Main Results:

  • Metformin treatment significantly up-regulated miR-107 expression in GC cells.
  • Increased miR-107 expression further inhibited cell proliferation in metformin-treated GC cells.
  • Mitogen-activated protein kinase 8 (MAPK8) was identified as a common target of metformin and miR-107, with its expression linked to GC patient survival and immune cell infiltration.

Conclusions:

  • miR-107 plays a crucial role in mediating the anti-cancer effects of metformin in gastric cancer.
  • The miR-107/MAPK8 pathway represents a novel therapeutic target for gastric cancer.
  • This study provides a new strategy for enhancing metformin-based treatments for GC.

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