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Published on: May 1, 2020
Clinical significance of mTOR and eIF4E expression in invasive ductal carcinoma
Aims And Background:
Mammalian target of rapamycin (mTOR) is one of the serine-threonine protein kinases and plays an important regulatory role in cell growth. Eukaryotic translation initiation factor 4E (eIF4E) and 4E binding protein (4EBP) are the downstream proteins of mTOR signaling pathway and are the most efficient speed regulator of eukaryotic mRNA translation. The aim of the study was to investigate the clinical significance of mTOR, eIF4E and 4EBPs expression in invasive ductal carcinoma.
Methods:
Fresh biopsy specimens of invasive ductal carcinoma tissues and normal breast tissues were collected from 45 patients with breast cancer. The expressions of mTOR, eIF4E and 4EBPs in specimens were detected by an immunohistochemical SP method, and the relationship of mTOR, eIF4E and 4EBPS expressions and of their expressions with tumor metastasis were analyzed.
Results:
Expressions of mTOR, eIF4E and 4EBPs in invasive ductal carcinoma were significantly higher than in normal breast tissue (P <0.05). mTOR expression was positively correlated with eIF4E and 4EBP expression in invasive ductal carcinoma (P <0.05). The positive rates of mTOR, eIF4E and 4EBPs in patients with lymph node metastasis were significantly higher than in patients without lymph node metastasis (P <0.05).
Conclusions:
Increased expressions of mTOR and eIF4E in invasive ductal carcinoma may be correlated with the occurrence and metastasis of breast cancer.
Insights
Increased expression of mTOR and eIF4E in invasive ductal carcinoma may indicate a higher risk of breast cancer occurrence and metastasis. This study analyzed protein levels in patient tissues to understand their clinical significance.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Mammalian target of rapamycin (mTOR) is a key regulator of cell growth.
- Eukaryotic translation initiation factor 4E (eIF4E) and 4E binding protein (4EBP) are downstream effectors in the mTOR signaling pathway, controlling mRNA translation.
- Aberrant mTOR signaling is implicated in various cancers, including breast cancer.
Purpose of the Study:
- To investigate the clinical significance of mTOR, eIF4E, and 4EBP expression in invasive ductal carcinoma.
- To determine the correlation between the expression of these proteins and clinicopathological features, particularly tumor metastasis.
Main Methods:
- Immunohistochemical SP method was used to detect the expression of mTOR, eIF4E, and 4EBPs.
- Expression levels were analyzed in 45 invasive ductal carcinoma tissue specimens and matched normal breast tissues.
- Statistical analysis was performed to assess correlations between protein expressions and lymph node metastasis.
Main Results:
- Expressions of mTOR, eIF4E, and 4EBPs were significantly elevated in invasive ductal carcinoma compared to normal breast tissue (P <0.05).
- A positive correlation was observed between mTOR expression and the expression of eIF4E and 4EBP in invasive ductal carcinoma (P <0.05).
- Higher positive rates of mTOR, eIF4E, and 4EBPs were found in patients with lymph node metastasis than in those without (P <0.05).
Conclusions:
- Elevated expression of mTOR and eIF4E in invasive ductal carcinoma is associated with an increased risk of breast cancer occurrence.
- The findings suggest that mTOR and eIF4E may play a role in the metastasis of breast cancer.
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