Overexpression of p-4EBP1 associates with peIF4E and predicts poor prognosis for non-small cell lung cancer patients with resection

10Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Eukaryotic initiation factor 4E (eIF4E) and its phosphorylated form (p-eIF4E) play a crucial role in the protein synthesis, both are under regulation of eIF4E-binding protein 1 (4EBP1) and mitogen-activated protein kinase (MAPK)-interacting kinases (MNKs). This study aims to explore the potential prognostic significance of p-4EBP1 and p-eIF4E in NSCLC patients. The expression of p-4EBP1 and p-eIF4E in NSCLC patients was detected by immunohistochemistry (IHC) staining in tissue microarrays (TMAs) containing 354 NSCLC and 53 noncancerous lung tissues (Non-CLT). The overexpression percentage of p-4EBP1 and peIF4E in lung squamous cell carcinoma (SCC) and adenocarcinoma (ADC) was significantly higher than that of Non-CLT. P-4EBP1 expression in patients with advanced clinical stage was higher than that in early stage. Expression of p-4EBP1 had a positive relationship with p-eIF4E expression both in lung SCC and ADC. NSCLC patients with high expression of p-4EBP1 and p-eIF4E alone or in combination had a lower survival rate than that of other phenotypes. For NSCLC patients, p-4EBP1 is an independent poor prognostic factor as well as clinical stage, LNM and pathological grade. Overexpression of p-4EBP1 and p-eIF4E might be novel prognostic marker for NSCLC, who possesses potential application value for NSCLC targeted therapy.

Cite

CITATION STYLE

APA

Tang, Y., Luo, J., Yang, Liu, S., Zheng, H., Zhan, Y., … Wen, Q. (2022). Overexpression of p-4EBP1 associates with peIF4E and predicts poor prognosis for non-small cell lung cancer patients with resection. PLoS ONE, 17(6 June). https://doi.org/10.1371/journal.pone.0265465

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free