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Updated: Jan 19, 2026

A "Patient-Like" Orthotopic Syngeneic Mouse Model of Hepatocellular Carcinoma Metastasis
Published on: October 24, 2015
Positive Correlative over-Expression between eIF4E and Snail in Nasopharyngeal Carcinoma Promotes its Metastasis and
Yunhong Yao1, Tianyun Pang2, Ying Cheng1
1Department of Pathology, Cancer Research Institute of Guangdong Medical University, Dongguan, 523808, China.
Abstract:
EIF4E is the rate-limiting factor in the mRNA translation of specific set of oncogenes. Snail is the core transcription factor of epithelial-mesenchymal transition (EMT), a key step of cancer metastasis. The connection between the two oncoproteins has not been well established in the human cancer tissues and in nasopharyngeal carcinoma (NPC). Here we showed that the positive correlative over-expression was seen between eIF4E and Snail in NPC tissues, and the expression was significantly higher in the metastatic NPC than in the un-metastatic NPC. In NPC cells, eIF4E knockdown significantly reduced Snail mRNA and protein levels, increased the mRNA level of E-cad (a direct downstream gene of Snail and a negative EMT marker), attenuated the invasive ability of the cells, and sensitized the cells to cisplatin in invasion. In contrast, enforced the expression of eIF4E significantly increased Snail mRNA and protein levels, and promoted the invasive ability in NPC cells. Under the condition of the high eIF4E expression, Snail knockdown significantly increased E-cad mRNA level and weaken the invasive ability of NPC cells. Finally, eIF4E directly bound Snail mRNA for translation initiation displayed by the RIP assay. Therefore, the results firstly suggested that eIF4E enhanced the Snail expression in both transcription and translation manner in human cancer tissues and targeting the eIF4E/Snail axis might intervene with the EMT and metastasis of NPC. This finding provided a new clue for further understanding the metastatic mechanism of human cancers and for preventing and treating NPC metastasis.
Insights
Eukaryotic initiation factor 4E (eIF4E) boosts Snail expression, promoting cancer metastasis in nasopharyngeal carcinoma (NPC). Targeting this eIF4E/Snail pathway may offer new treatments for NPC metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Metastasis Research
Background:
- Eukaryotic initiation factor 4E (eIF4E) regulates oncogene translation.
- Snail is a key transcription factor in epithelial-mesenchymal transition (EMT), crucial for cancer metastasis.
- The relationship between eIF4E and Snail in nasopharyngeal carcinoma (NPC) is not well understood.
Purpose of the Study:
- To investigate the functional connection between eIF4E and Snail in NPC.
- To determine the role of eIF4E in regulating Snail expression and NPC cell invasion.
- To explore the potential of targeting the eIF4E/Snail axis for NPC metastasis intervention.
Main Methods:
- Analysis of eIF4E and Snail expression in NPC tissues.
- Knockdown and overexpression experiments in NPC cells.
- Measurement of E-cadherin (E-cad) mRNA levels.
- Assessment of NPC cell invasive ability.
- RNA immunoprecipitation (RIP) assay to confirm direct binding.
Main Results:
- Positive correlation between eIF4E and Snail overexpression in NPC tissues, higher in metastatic cases.
- eIF4E knockdown reduced Snail levels, increased E-cad, and attenuated NPC cell invasion.
- eIF4E overexpression increased Snail levels and promoted NPC cell invasion.
- eIF4E directly binds to Snail mRNA, enhancing its translation.
Conclusions:
- eIF4E enhances Snail expression via both transcriptional and translational mechanisms in NPC.
- The eIF4E/Snail axis plays a critical role in promoting EMT and metastasis in NPC.
- Targeting the eIF4E/Snail pathway presents a potential therapeutic strategy for preventing and treating NPC metastasis.
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