Literature DB >> 21236475

Tyrosine kinase A receptor (trkA): a potential marker in epithelial ovarian cancer.

Verónica Tapia1, Fernando Gabler, Marcela Muñoz, Roberto Yazigi, Alfonso Paredes, Alberto Selman, Margarita Vega, Carmen Romero.   

Abstract

OBJECTIVES: To evaluate the role of trkA receptor as a potential tumor marker in serous epithelial ovarian cancer and its relationship with the angiogenic factors expression as vascular endothelial growth factor (VEGF) and nerve growth factor (NGF). Additionally, to examine whether NGF and VEGF secreted by epithelial ovarian cancer (EOC) explants and from epithelial ovarian cancer cell line (A2780) are involved in the process of angiogenesis, such as cellular proliferation, migration and differentiation of the human endothelial cell line (EA.hy926).
METHODS: The mRNA levels of VEGF, NGF and trkA receptors were measured using PCR in 60 ovarian samples. Cellular localization and semi-quantitative estimation of VEGF, NGF, total trkA and p-trkA was performed using IHC in epithelial cells. NGF, total trkA and p-trkA protein were also evaluated in endothelial cells from the same tissues. Human endothelial cell line EA.hy926 was cultured with conditioned media obtained from both EOC explants and from the A2780 cell line, with or without NGF stimulus.
RESULTS: Significantly higher levels of NGF, total trkA and p-trkA protein expressions were observed in epithelial and endothelial cells in poorly differentiated EOC versus normal ovary. Interestingly, the p-trkA receptor expression level showed the most significant difference and its presence was only found in borderline tumor and EOC samples indicating the importance of trkA receptor in EOC as a potential tumor marker. A significant increase in proliferation, migration and differentiation of EA.hy926 cells was observed with NGF, and this effect was significantly reverted when NGF was immuno-blocked and when a trkA inhibitor was used, showing that NGF is an important angiogenic factor in EOC by activating its trkA receptor.
CONCLUSION: These results indicate that p-trkA may be considered as a new potential tumor marker in EOC, and that NGF may also act as a direct angiogenic factor in EOC.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21236475     DOI: 10.1016/j.ygyno.2010.12.341

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  19 in total

1.  Transient receptor potential canonical channels are required for in vitro endothelial tube formation.

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Journal:  J Biol Chem       Date:  2011-12-27       Impact factor: 5.157

2.  Toward an integrative analysis of the tumor microenvironment in ovarian epithelial carcinoma.

Authors:  Ryan N Serio
Journal:  Cancer Microenviron       Date:  2011-11-23

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Review 5.  Stress Hormones: Emerging Targets in Gynecological Cancers.

Authors:  Guoqiang Chen; Lei Qiu; Jinghai Gao; Jing Wang; Jianhong Dang; Lingling Li; Zhijun Jin; Xiaojun Liu
Journal:  Front Cell Dev Biol       Date:  2021-07-09

Review 6.  Role of nerve growth factor and its TRKA receptor in normal ovarian and epithelial ovarian cancer angiogenesis.

Authors:  Carolina Vera; Verónica Tapia; Margarita Vega; Carmen Romero
Journal:  J Ovarian Res       Date:  2014-08-10       Impact factor: 4.234

7.  Role of dihydrotestosterone (DHT) on TGF-β1 signaling pathway in epithelial ovarian cancer cells.

Authors:  Karla Kohan-Ivani; Fernando Gabler; Alberto Selman; Margarita Vega; Carmen Romero
Journal:  J Cancer Res Clin Oncol       Date:  2015-06-20       Impact factor: 4.553

8.  Nerve growth factor modulates the tumor cells migration in ovarian cancer through the WNT/β-catenin pathway.

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Review 9.  Nerve growth factor: from the early discoveries to the potential clinical use.

Authors:  Luigi Aloe; Maria Luisa Rocco; Patrizia Bianchi; Luigi Manni
Journal:  J Transl Med       Date:  2012-11-29       Impact factor: 5.531

10.  Detecting Gene Rearrangements in Patient Populations Through a 2-Step Diagnostic Test Comprised of Rapid IHC Enrichment Followed by Sensitive Next-Generation Sequencing.

Authors:  Danielle A Murphy; Heather A Ely; Robert Shoemaker; Aaron Boomer; Brady P Culver; Ian Hoskins; Josh D Haimes; Ryan D Walters; Diane Fernandez; Joshua A Stahl; Jeeyun Lee; Kyoung-Mee Kim; Jennifer Lamoureux; Jason Christiansen
Journal:  Appl Immunohistochem Mol Morphol       Date:  2017-08
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