Literature DB >> 21252859

Molecular mechanisms of epidermal growth factor receptor overexpression in patients with cervical cancer.

Marlies Schrevel1, Arko Gorter, Sandra M Kolkman-Uljee, J Baptist M Z Trimbos, Gert Jan Fleuren, Ekaterina S Jordanova.   

Abstract

The epidermal growth factor receptor is overexpressed in 70-90% of cervical cancers. Previously, we have shown that epidermal growth factor receptor overexpression independently predicts poor prognosis in cervical cancer patients, which makes it a potential therapeutic target. The aim of this study was to systematically analyze the molecular mechanism leading to epidermal growth factor receptor overexpression in cervical cancer. All experiments were performed on archival paraffin-embedded material. In 166 cervical cancer patients, cytoplasmic, membrane and phosphorylated epidermal growth factor receptor protein expression were studied in association with patient survival. Membrane epidermal growth factor receptor overexpression was associated with poor disease-specific survival (P=0.027). This association was particularly present in human papillomavirus 16-positive patients (P=0.029). We analyzed whether epidermal growth factor receptor overexpression was caused by gene amplification using fluorescence in situ hybridization. Epidermal growth factor receptor gene copy number was linked to chromosome 7 ploidy, as no gene amplification could be detected when corrected for chromosome 7 centromeric signals. Chromosome 7 aneuploidy was associated with membrane epidermal growth factor receptor overexpression (P=0.013). Additional mutation analysis was performed by sequencing pure, flow-sorted tumor cells, but no mutations were detected. Furthermore, human papillomavirus 16 E5 and E6 oncogene mRNA expression was measured, using quantitative real-time polymerase chain reaction, to determine the association between the human papillomavirus and epidermal growth factor receptor overexpression. High human papillomavirus 16 E5 and E6 mRNA expression were associated with decreased survival (P=0.045 and 0.047, respectively). High human papillomavirus 16 E6 mRNA expression was associated with membrane epidermal growth factor receptor overexpression (P=0.013). This is the first study performed on cancer patient material showing that chromosome 7 aneuploidy and high human papillomavirus 16 E6 mRNA expression lead to membrane epidermal growth factor receptor overexpression in cervical cancer.

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Year:  2011        PMID: 21252859     DOI: 10.1038/modpathol.2010.239

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  20 in total

1.  E5 can be expressed in anal cancer and leads to epidermal growth factor receptor-induced invasion in a human papillomavirus 16-transformed anal epithelial cell line.

Authors:  Erin Isaacson Wechsler; Sharof Tugizov; Rossana Herrera; Maria Da Costa; Joel M Palefsky
Journal:  J Gen Virol       Date:  2018-04-06       Impact factor: 3.891

2.  Autocrine expression of the epidermal growth factor receptor ligand heparin-binding EGF-like growth factor in cervical cancer.

Authors:  Marlies Schrevel; E Michelle Osse; Frans A Prins; J Baptist M Z Trimbos; Gert Jan Fleuren; Arko Gorter; Ekaterina S Jordanova
Journal:  Int J Oncol       Date:  2017-05-03       Impact factor: 5.650

3.  Investigation of molecular mechanisms underlying JAK/STAT signaling pathway in HPV-induced cervical carcinogenesis using 'omics' approach.

Authors:  Kulbhushan Thakur; Divya Janjua; Gauri Shishodia; Arun Chhokar; Nikita Aggarwal; Joni Yadav; Tanya Tripathi; Apoorva Chaudhary; Anna Senrung; Alok Chandra Bharti
Journal:  Med Oncol       Date:  2022-10-12       Impact factor: 3.738

4.  Epidermal Growth Factor Receptor and Transforming Growth Factor β Signaling Pathways Cooperate To Mediate Chlamydia Pathogenesis.

Authors:  Joseph U Igietseme; James Partin; Zenas George; Yusuf Omosun; Jason Goldstein; Kahaliah Joseph; Debra Ellerson; Francis O Eko; Jan Pohl; Claudiu Bandea; Carolyn M Black
Journal:  Infect Immun       Date:  2020-03-23       Impact factor: 3.441

5.  TACC3 is essential for EGF-mediated EMT in cervical cancer.

Authors:  Geun-Hyoung Ha; Jung-Lye Kim; Eun-Kyoung Breuer; Eun-Kyoung Yim Breuer
Journal:  PLoS One       Date:  2013-08-01       Impact factor: 3.240

6.  Mutation analysis of EGFR and its correlation with the HPV in Indian cervical cancer patients.

Authors:  Rehana Qureshi; Himanshu Arora; Shilpi Biswas; Ahmad Perwez; Afreen Naseem; Saima Wajid; Gauri Gandhi; Moshahid Alam Rizvi
Journal:  Tumour Biol       Date:  2016-01-14

7.  CXCR7 expression is associated with disease-free and disease-specific survival in cervical cancer patients.

Authors:  M Schrevel; R Karim; N T ter Haar; S H van der Burg; J B M Z Trimbos; G J Fleuren; A Gorter; E S Jordanova
Journal:  Br J Cancer       Date:  2012-04-24       Impact factor: 7.640

8.  HPV16 Down-Regulates the Insulin-Like Growth Factor Binding Protein 2 to Promote Epithelial Invasion in Organotypic Cultures.

Authors:  Adam Pickard; Simon S McDade; Marie McFarland; W Glenn McCluggage; Cosette M Wheeler; Dennis J McCance
Journal:  PLoS Pathog       Date:  2015-06-24       Impact factor: 6.823

9.  An Optimization-Driven Analysis Pipeline to Uncover Biomarkers and Signaling Paths: Cervix Cancer.

Authors:  Enery Lorenzo; Katia Camacho-Caceres; Alexander J Ropelewski; Juan Rosas; Michael Ortiz-Mojer; Lynn Perez-Marty; Juan Irizarry; Valerie Gonzalez; Jesús A Rodríguez; Mauricio Cabrera-Rios; Clara Isaza
Journal:  Microarrays (Basel)       Date:  2015-06

10.  The Hippo/YAP pathway interacts with EGFR signaling and HPV oncoproteins to regulate cervical cancer progression.

Authors:  Chunbo He; Dagan Mao; Guohua Hua; Xiangmin Lv; Xingcheng Chen; Peter C Angeletti; Jixin Dong; Steven W Remmenga; Kerry J Rodabaugh; Jin Zhou; Paul F Lambert; Peixin Yang; John S Davis; Cheng Wang
Journal:  EMBO Mol Med       Date:  2015-11       Impact factor: 12.137

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