Clinical significance of mTOR and eIF4E expression in invasive ductal carcinoma

Tumori
|October 25, 2014
PubMed
Abstract

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.

Related Concept Videos

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...
3.6K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

1.4K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
5.1K
Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
6.3K