Literature DB >> 27919967

Epithelial-Mesenchymal Expression Phenotype of Primary Melanoma and Matched Metastases and Relationship with Overall Survival.

Shaofeng Yan1, Britt M Holderness2, Zhongze Li3, Gregory D Seidel1, Jiang Gui4, Jan L Fisher5, Marc S Ernstoff6.   

Abstract

E-Cadherin and N-cadherin are important components of epithelial-mesenchymal transition (EMT). The majority of studies on EMT in melanoma have been performed with cultured cell lines or pooled melanoma samples. The goal of our study was to evaluate the expression of E-cadherin and N-cadherin in matched tissue samples from primary and metastatic sites of melanoma and to determine the correlation with survival outcome. We analyzed tissues from 42 melanoma primary lesions and their corresponding metastases, as well as 53 benign nevi, for expression levels of E-cadherin and N-cadherin using immunohistochemical methods. There were heterogenous expression patterns of E- and N-cadherin in both primary and metastatic melanomas. Overall, metastatic tumor showed a decrease in E-cadherin expression and an increase in N-cadherin expression compared to the primary tumor, although the difference did not reach statistical significance (p=0.24 and 0.28 respectively). A switch of membranous expression from E-cadherin to N-cadherin from primary to metastatic melanoma was seen in eight patients (19%). Aberrant E-cadherin expression (defined as negative to weak membranous E-cadherin or positive nuclear E-cadherin expression) was more frequently observed in metastatic than in primary melanomas (p=0.03). Multivariate analysis showed that absence of N-cadherin expression in primary melanomas and the presence of aberrant E-cadherin expression in primary melanomas and metastatic melanomas was associated with a significantly worse overall survival. Our data support the importance of E-cadherin and N-cadherin proteins in melanoma progression and patient survival. Copyright
© 2016 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved.

Entities:  

Keywords:  E-cadherin; Epithelial–mesenchymal transition; N-cadherin; melanoma; metastasis

Mesh:

Substances:

Year:  2016        PMID: 27919967      PMCID: PMC5576452          DOI: 10.21873/anticanres.11243

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  32 in total

1.  Alterations in cadherin and catenin expression during the biological progression of melanocytic tumours.

Authors:  D S Sanders; K Blessing; G A Hassan; R Bruton; J R Marsden; J Jankowski
Journal:  Mol Pathol       Date:  1999-06

2.  Influence of the cytoplasmic domain of E-cadherin on endogenous N-cadherin expression in malignant melanoma.

Authors:  S Kuphal; A K Bosserhoff
Journal:  Oncogene       Date:  2006-01-12       Impact factor: 9.867

Review 3.  Reassessing epithelial to mesenchymal transition as a prerequisite for carcinoma invasion and metastasis.

Authors:  Jason J Christiansen; Ayyappan K Rajasekaran
Journal:  Cancer Res       Date:  2006-09-01       Impact factor: 12.701

Review 4.  Adhesion, migration and communication in melanocytes and melanoma.

Authors:  Nikolas K Haass; Keiran S M Smalley; Ling Li; Meenhard Herlyn
Journal:  Pigment Cell Res       Date:  2005-06

5.  Clinicopathologic significance of dysadherin expression in cutaneous malignant melanoma: immunohistochemical analysis of 115 patients.

Authors:  Aya Nishizawa; Yukihiro Nakanishi; Kimio Yoshimura; Yuko Sasajima; Naoya Yamazaki; Akifumi Yamamoto; Katsumi Hanada; Yae Kanai; Setsuo Hirohashi
Journal:  Cancer       Date:  2005-04-15       Impact factor: 6.860

6.  Cadherin switch from E- to N-cadherin in melanoma progression is regulated by the PI3K/PTEN pathway through Twist and Snail.

Authors:  L Hao; J R Ha; P Kuzel; E Garcia; S Persad
Journal:  Br J Dermatol       Date:  2012-05-08       Impact factor: 9.302

Review 7.  The role of epithelial-mesenchymal transition in cancer pathology.

Authors:  Marcello Guarino; Barbara Rubino; Gianmario Ballabio
Journal:  Pathology       Date:  2007-06       Impact factor: 5.306

8.  Prognostic significance of cadherin-based adhesion molecules in cutaneous malignant melanoma.

Authors:  Gretchen M Kreizenbeck; Aaron J Berger; Antonio Subtil; David L Rimm; Bonnie E Gould Rothberg
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2008-04       Impact factor: 4.254

9.  Targeting N-cadherin increases vascular permeability and differentially activates AKT in melanoma.

Authors:  Ryan S Turley; Yoshihiro Tokuhisa; Hiroaki Toshimitsu; Michael E Lidsky; James C Padussis; Andrew Fontanella; Wanleng Deng; Christina K Augustine; Georgia M Beasley; Michael A Davies; Mark W Dewhirst; Douglas S Tyler
Journal:  Ann Surg       Date:  2015-02       Impact factor: 12.969

10.  E-cadherin is the major mediator of human melanocyte adhesion to keratinocytes in vitro.

Authors:  A Tang; M S Eller; M Hara; M Yaar; S Hirohashi; B A Gilchrest
Journal:  J Cell Sci       Date:  1994-04       Impact factor: 5.285

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2.  Melanoma protective antitumor immunity activated by catalytic DNA.

Authors:  Hong Cai; Eun-Ae Cho; Yue Li; Jim Sockler; Christopher R Parish; Beng H Chong; Jarem Edwards; Tristan J Dodds; Peter M Ferguson; James S Wilmott; Richard A Scolyer; Gary M Halliday; Levon M Khachigian
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3.  Role of epithelial-mesenchymal transition involved molecules in the progression of cutaneous melanoma.

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Review 4.  Significance of epithelial-to-mesenchymal transition inducing transcription factors in predicting distance metastasis and survival in patients with colorectal cancer: A systematic review and meta-analysis.

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Journal:  J Res Med Sci       Date:  2020-06-30       Impact factor: 1.852

Review 5.  Neural crest and cancer: Divergent travelers on similar paths.

Authors:  Kristin L Gallik; Randall W Treffy; Lynne M Nacke; Kamil Ahsan; Manuel Rocha; Abigail Green-Saxena; Ankur Saxena
Journal:  Mech Dev       Date:  2017-09-06       Impact factor: 1.882

Review 6.  Upregulated N-cadherin expression is associated with poor prognosis in epithelial-derived solid tumours: A meta-analysis.

Authors:  Yong Luo; Ting Yu; Qiongwen Zhang; Qingyu Fu; Yuzhu Hu; Mengmeng Xiang; Haoning Peng; Tianying Zheng; Li Lu; Huashan Shi
Journal:  Eur J Clin Invest       Date:  2018-02-25       Impact factor: 4.686

7.  Zebrafish modeling reveals that SPINT1 regulates the aggressiveness of skin cutaneous melanoma and its crosstalk with tumor immune microenvironment.

Authors:  Elena Gómez-Abenza; Sofía Ibáñez-Molero; Diana García-Moreno; Inmaculada Fuentes; Leonard I Zon; Maria C Mione; María L Cayuela; Chiara Gabellini; Victoriano Mulero
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8.  FAM3B promotes progression of oesophageal carcinoma via regulating the AKT-MDM2-p53 signalling axis and the epithelial-mesenchymal transition.

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Journal:  J Cell Mol Med       Date:  2018-12-18       Impact factor: 5.310

9.  Mass Spectrometry-Based Proteomic Characterization of Cutaneous Melanoma Ectosomes Reveals the Presence of Cancer-Related Molecules.

Authors:  Magdalena Surman; Sylwia Kędracka-Krok; Dorota Hoja-Łukowicz; Urszula Jankowska; Anna Drożdż; Ewa Ł Stępień; Małgorzata Przybyło
Journal:  Int J Mol Sci       Date:  2020-04-22       Impact factor: 5.923

10.  Comparative Study of Transcriptomics-Based Scoring Metrics for the Epithelial-Hybrid-Mesenchymal Spectrum.

Authors:  Priyanka Chakraborty; Jason T George; Shubham Tripathi; Herbert Levine; Mohit Kumar Jolly
Journal:  Front Bioeng Biotechnol       Date:  2020-03-20
  10 in total

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