Influence of miR-376c-3p/SYF2 Axis on the Progression of Gastric Cancer

Bin Liu1, Guangchun Li1, Zhen Zhang1

  • 1Department of Gastroenterology, The Second Hospital of Shandong University, Jinan, China.

Insights

MicroRNA-376c-3p, a key player in cancer, was found to be downregulated in gastric cancer cells. Its restoration inhibits cancer cell proliferation and migration by targeting the SYF2 gene.

Area of Science:

  • Molecular Biology
  • Oncology
  • Gene Regulation

Background:

  • MicroRNA-376c-3p is implicated in human cancer progression.
  • Gastric cancer remains a significant global health concern, necessitating research into its underlying mechanisms.

Purpose of the Study:

  • To investigate the role of microRNA-376c-3p in human gastric cancer cell proliferation and migration.
  • To elucidate the molecular mechanism by which microRNA-376c-3p influences gastric cancer progression, focusing on its interaction with SYF2.

Main Methods:

  • Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to assess microRNA-376c-3p expression levels in gastric cancer cell lines versus normal cells.
  • The direct targeting relationship and functional impact of microRNA-376c-3p on SYF2 (pre-mRNA splicing factor) were analyzed.
  • Gain-of-function experiments involving microRNA-376c-3p mimic and SYF2 overexpression were performed to evaluate effects on cell behaviors.

Main Results:

  • MicroRNA-376c-3p expression was significantly downregulated in human gastric cancer cell lines compared to normal gastric cells.
  • MicroRNA-376c-3p was identified as a direct targeting molecule of SYF2, leading to reduced SYF2 expression.
  • Overexpression of microRNA-376c-3p suppressed gastric cancer cell proliferation and migration.
  • Conversely, overexpression of SYF2 counteracted the inhibitory effects of microRNA-376c-3p on gastric cancer cell behaviors.

Conclusions:

  • MicroRNA-376c-3p functions as a tumor suppressor in gastric cancer.
  • The inhibitory effect of microRNA-376c-3p on gastric cancer cell proliferation and migration is mediated through the direct targeting and downregulation of SYF2.

Related Concept Videos

Elastic Staining on Paraffin-embedded Slides of pT3N0M0 Gastric Cancer Tissue06:36

Elastic Staining on Paraffin-embedded Slides of pT3N0M0 Gastric Cancer Tissue

Here, we present a protocol of elastic staining to identify elastic fibers in pT3N0M0 gastric cancer tissues on formalin-fixed, paraffin-embedded sections. Subsequently, we describe a method to determine whether tumor cells invade beyond the elastic...
7.4K
Establishment of Gastric Cancer Patient-derived Xenograft Models and Primary Cell Lines08:42

Establishment of Gastric Cancer Patient-derived Xenograft Models and Primary Cell Lines

The current protocol describes methods to establish patient-derived xenograft (PDX) models and primary cancer cell lines from surgical gastric cancer samples. The methods provide a useful tool for drug development and cancer biology...
10.7K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
4.6K
Bioluminescent Orthotopic Model of Pancreatic Cancer Progression09:25

Bioluminescent Orthotopic Model of Pancreatic Cancer Progression

Improved understanding of pancreatic cancer biology is critically needed to enable the development of better therapeutic options to treat pancreatic cancer. To address this need, we demonstrate an orthotopic model of pancreatic cancer that permits non-invasive monitoring of cancer progression using in vivo bioluminescence...
27.5K
Microfluidic Co-culture of Renal Healthy and Tumor Epithelium to Model Kidney Cancer Progression06:29

Microfluidic Co-culture of Renal Healthy and Tumor Epithelium to Model Kidney Cancer Progression

Here, we present protocols that detail instructions for implementing 3D cell cultures using collagen and collagen-agarose matrixes in a microphysiological system. These protocols support renal proximal tubule and renal cell carcinoma spheroids co-culture, simulating in vivo conditions and enabling advanced investigation of kidney cancer cell...
1.2K
3D Cell-Printed Hypoxic Cancer-on-a-Chip for Recapitulating Pathologic Progression of Solid Cancer10:51

3D Cell-Printed Hypoxic Cancer-on-a-Chip for Recapitulating Pathologic Progression of Solid Cancer

Hypoxia is a hallmark of tumor microenvironment and plays a crucial role in cancer progression. This article describes the fabrication process of a hypoxic cancer-on-a-chip based on 3D cell-printing technology to recapitulate a hypoxia-related pathology of...
5.1K