Literature DB >> 19628077

Eukaryotic initiation factor 4E overexpression in triple-negative breast cancer predicts a worse outcome.

Anthony Flowers1, Quyen D Chu, Lori Panu, Carol Meschonat, Gloria Caldito, Mary Lowery-Nordberg, Benjamin D L Li.   

Abstract

BACKGROUND: Triple-negative (estrogen receptor [ER], progesterone receptor [PR], and HER2/neu receptor negative) breast neoplasms are typically high grade and portend a higher risk for relapse. Not being amendable to ER, PR, or HER2-targeted therapy, adjuvant cytotoxic chemotherapy remains the only option. High eukaryotic Initiation Factor 4E (eIF4E) overexpression in tumor specimens is an independent predictor for relapse in breast cancer, perhaps secondary to tousled-like kinase 1B upregulation and subsequent doxorubicin resistance. In this prospective study, eIF4E elevation in triple-negative breast cancer (TNBC) specimens was studied to determine its effect on cancer outcome.
METHODS: A prospective study of 103 TNBC patients was initiated. Tumor specimens were quantified for eIF4E expression using Western blots. Clinical outcomes data were collected after standardized adjuvant treatment and surveillance protocols. Primary end points were cancer recurrence and cancer-related death. The eIF4E levels in cancer specimens were quantified as x-fold over benign samples from noncancer patients. Statistical procedures performed include survival analysis by Kaplan-Meier method, log-rank test, Cox proportional hazards regression model, and the chi-square test.
RESULTS: Levels of eIF4E were categorized into 3 tertiles. Among 103 patients, 36 were in the low group (< or =7.5-fold), 40 were in the intermediate group (7.5- to 15-fold), and 27 were in the high group (> or =15-fold). Patients with triple-negative neoplasms that were in the high eIF4E group had greater rates of cancer recurrence (P = .04) and cancer-related death (P = .02) than the low eIF4E group. Among patients with node-negative disease, high eIF4E overexpression in tumor specimens continues to portend a greater rate of cancer recurrence (P = .02), and a higher rate of cancer death (P = .03) than those in the low eIF4E group.
CONCLUSION: TNBC patients with high eIF4E overexpression are more likely to recur and die from cancer recurrence. High eIF4E seems to be a significant prognostic marker, even in TNBC patients.

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Year:  2009        PMID: 19628077     DOI: 10.1016/j.surg.2009.05.010

Source DB:  PubMed          Journal:  Surgery        ISSN: 0039-6060            Impact factor:   3.982


  15 in total

1.  The role of MNK proteins and eIF4E phosphorylation in breast cancer cell proliferation and survival.

Authors:  Matthew J Wheater; Peter Wm Johnson; Jeremy P Blaydes
Journal:  Cancer Biol Ther       Date:  2010-10-01       Impact factor: 4.742

2.  EIF4E over-expresses and enhances cell proliferation and cell cycle progression in nasopharyngeal carcinoma.

Authors:  Mengyan Wu; Yingxia Liu; Xiaoqing Di; Haixian Kang; Hua Zeng; Yi Zhao; Kangrong Cai; Tianyun Pang; Sen Wang; Yunhong Yao; Xinrong Hu
Journal:  Med Oncol       Date:  2013-01-01       Impact factor: 3.064

3.  Knockdown of eIF4E suppresses cell growth and migration, enhances chemosensitivity and correlates with increase in Bax/Bcl-2 ratio in triple-negative breast cancer cells.

Authors:  Fei-fei Zhou; Min Yan; Gui-fang Guo; Fang Wang; Hui-juan Qiu; Fei-meng Zheng; Yan Zhang; Qiang Liu; Xiao-feng Zhu; Liang-ping Xia
Journal:  Med Oncol       Date:  2010-07-22       Impact factor: 3.064

4.  Targeting eukaryotic translation initiation factor 4E (eIF4E) in cancer.

Authors:  Andrew C Hsieh; Davide Ruggero
Journal:  Clin Cancer Res       Date:  2010-08-11       Impact factor: 12.531

5.  Detection of eukaryotic translation initiation factor 4E and its clinical significance in hepatocellular carcinoma.

Authors:  Xiao-Lin Wang; Hong-Pei Cai; Jun-Hui Ge; Xiao-Feng Su
Journal:  World J Gastroenterol       Date:  2012-05-28       Impact factor: 5.742

6.  Targeted Dual pH-Sensitive Lipid ECO/siRNA Self-Assembly Nanoparticles Facilitate In Vivo Cytosolic sieIF4E Delivery and Overcome Paclitaxel Resistance in Breast Cancer Therapy.

Authors:  Maneesh Gujrati; Amita M Vaidya; Margaret Mack; Dayton Snyder; Anthony Malamas; Zheng-Rong Lu
Journal:  Adv Healthc Mater       Date:  2016-10-10       Impact factor: 9.933

Review 7.  Oncogenic AKTivation of translation as a therapeutic target.

Authors:  A C Hsieh; M L Truitt; D Ruggero
Journal:  Br J Cancer       Date:  2011-07-19       Impact factor: 7.640

8.  Translation initiation complex eIF4F is a therapeutic target for dual mTOR kinase inhibitors in non-Hodgkin lymphoma.

Authors:  Christos Demosthenous; Jing Jing Han; Mary J Stenson; Matthew J Maurer; Linda E Wellik; Brian Link; Kristen Hege; Ahmet Dogan; Eduardo Sotomayor; Thomas Witzig; Mamta Gupta
Journal:  Oncotarget       Date:  2015-04-20

9.  First MNKs degrading agents block phosphorylation of eIF4E, induce apoptosis, inhibit cell growth, migration and invasion in triple negative and Her2-overexpressing breast cancer cell lines.

Authors:  Senthilmurugan Ramalingam; Lalji Gediya; Andrew K Kwegyir-Afful; Vidya P Ramamurthy; Puranik Purushottamachar; Hannah Mbatia; Vincent C O Njar
Journal:  Oncotarget       Date:  2014-01-30

10.  Overexpression of eIF4E in colorectal cancer patients is associated with liver metastasis.

Authors:  Tao Xu; Yuanyuan Zong; Lipan Peng; Shuai Kong; Mingliang Zhou; Jianqiang Zou; Jinglei Liu; Ruizheng Miao; Xichao Sun; Leping Li
Journal:  Onco Targets Ther       Date:  2016-02-19       Impact factor: 4.147

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