Literature DB >> 29162497

Expression signatures of early-stage and advanced medaka melanomas.

Barbara Klotz1, Susanne Kneitz2, Martina Regensburger2, Lena Hahn2, Michael Dannemann3, Janet Kelso3, Birgit Nickel3, Yuan Lu4, William Boswell4, John Postlethwait5, Wesley Warren6, Manfred Kunz7, Ronald B Walter4, Manfred Schartl8.   

Abstract

Melanoma is one of the most aggressive tumors with a very low survival rate once metastasized. The incidence of newly detected cases increases every year suggesting the necessity of development and application of innovative treatment strategies. Human melanoma develops from melanocytes localized in the epidermis of the skin to malignant tumors because of deregulated effectors influencing several molecular pathways. Despite many advances in describing the molecular changes accompanying melanoma formation, many critical and clinically relevant molecular features of the transformed pigment cells and the underlying mechanisms are largely unknown. To contribute to a better understanding of the molecular processes of melanoma formation, we use a transgenic medaka melanoma model that is well suited for the investigation of melanoma tumor development because fish and human melanocytes are both localized in the epidermis. The purpose of our study was to gain insights into melanoma development from the first steps of tumor formation up to melanoma progression and to identify gene expression patterns that will be useful for monitoring treatment effects in drug screening approaches. Comparing transcriptomes from juvenile fish at the tumor initiating stage with nevi and advanced melanoma of adults, we identified stage specific expression signatures and pathways that are characteristic for the development of medaka melanoma, and are also found in human malignancies.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Gene expression signature; Medaka; Melanoma; RNA-sequencing; Transcriptome; Transgenic fish model

Mesh:

Substances:

Year:  2017        PMID: 29162497      PMCID: PMC5936653          DOI: 10.1016/j.cbpc.2017.11.005

Source DB:  PubMed          Journal:  Comp Biochem Physiol C Toxicol Pharmacol        ISSN: 1532-0456            Impact factor:   3.228


  64 in total

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