Overexpressed eIF4E Is Functionally Active in Surgical Margins of Head and Neck Cancer Patients via Activation of the Akt/Mammalian Target of Rapamycin Pathway

• Published in: Clinical cancer research 2004-09, Vol.10 (17), p.5820-5827
• Main Authors: NATHAN, Cherie-Ann O, AMIRGHAHARI, Nazanin, ABREO, Fleurette, XIAOHUA RONG, CALDITO, Gloria, JONES, M. Lamar, HUIJUAN ZHOU, SMITH, Melanie, KIMBERLY, Donnellan, GLASS, Jonathan
• Format: Article
• Language: English
• Subjects: Adaptor Proteins, Signal Transducing; Adult; Aged; Antineoplastic agents; Biological and medical sciences; Blotting, Western; Carcinoma, Squamous Cell - metabolism; Carcinoma, Squamous Cell - pathology; Carrier Proteins - metabolism; Eukaryotic Initiation Factor-4E - metabolism; Head and Neck Neoplasms - metabolism; Head and Neck Neoplasms - pathology; Humans; Immunoprecipitation; Medical sciences; Middle Aged; Pharmacology. Drug treatments; Phosphoproteins - metabolism; Phosphorylation; Protein Kinases - metabolism; Protein-Serine-Threonine Kinases - metabolism; Proto-Oncogene Proteins - metabolism; Proto-Oncogene Proteins c-akt; Ribosomal Protein S6 Kinases, 70-kDa - metabolism; Risk Factors; Signal Transduction; TOR Serine-Threonine Kinases; Tumors
• ISSN: 1078-0432; 1557-3265
• DOI: 10.1158/1078-0432.CCR-03-0483

Purpose: Overexpression of eIF4E in surgical margins of head and neck cancer patients is an independent risk factor for recurrence. We hypothesize that overexpressed eIF4E is functionally active in tumor margins through activation of the Akt/mammalian target of rapamycin (mTOR) pathway Experimental Design: Western blots and/or immunohistochemistry were performed to determine whether phosphorylation of mTOR and activation of its downstream molecules eIF4E-binding protein-1 (4E-BP1) and p70 S6 kinase and the upstream modulator of mTOR, Akt, were expressed in margins overexpressing eIF4E. Results: There was a significant association between phospho-4E-BP1 and eIF4E expression of a margin or a significant difference in phospho-4E-BP1 expression between the eIF4E-positive and -negative margins ( P < 0.01). A significant association between eIF4E and phospho-p70 S6 kinase as well as eIF4E and phospho-mTOR was also noted ( P < 0.05). Western blot analysis indicated a highly significant difference in the phosphorylation status of 4E-BP1 between tumors and resection margins. A total of 89% of the 4E-BP1-expressing margins expressed more of the phosphorylated (β, γ, and δ) isoforms, whereas 81% of the 4E-BP1-expressing tumors expressed more of the unphosphorylated α isoform. A similar difference in Akt activation was noted between eIF4E-positive margins and tumors ( P < 0.05). Conclusions: Overexpression of eIF4E is functionally active in tumor margins through activation of the Akt/mTOR signaling pathway. The greater degree of expression of downstream targets and upstream regulators of mTOR in margins compared with the tumors indicates preferential activation of the Akt/mTOR signaling pathway in margins overexpressing eIF4E. Rapamycin analogs can potentially be used as adjuvant therapy for patients with eIF4E-positive margins.