Literature DB >> 25533096

N-cadherin antagonists as oncology therapeutics.

Orest W Blaschuk1.   

Abstract

The cell adhesion molecule (CAM), N-cadherin, has emerged as an important oncology therapeutic target. N-cadherin is a transmembrane glycoprotein mediating the formation and structural integrity of blood vessels. Its expression has also been documented in numerous types of poorly differentiated tumours. This CAM is involved in regulating the proliferation, survival, invasiveness and metastasis of cancer cells. Disruption of N-cadherin homophilic intercellular interactions using peptide or small molecule antagonists is a promising novel strategy for anti-cancer therapies. This review discusses: the discovery of N-cadherin, the mechanism by which N-cadherin promotes cell adhesion, the role of N-cadherin in blood vessel formation and maintenance, participation of N-cadherin in cancer progression, the different types of N-cadherin antagonists and the use of N-cadherin antagonists as anti-cancer drugs.
© 2014 The Author(s) Published by the Royal Society. All rights reserved.

Entities:  

Keywords:  ADH-1; N-cadherin antagonists; angiogenesis; cancer; endothelial cells

Mesh:

Substances:

Year:  2015        PMID: 25533096      PMCID: PMC4275908          DOI: 10.1098/rstb.2014.0039

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  38 in total

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3.  Identification of a cadherin cell adhesion recognition sequence.

Authors:  O W Blaschuk; R Sullivan; S David; Y Pouliot
Journal:  Dev Biol       Date:  1990-05       Impact factor: 3.582

4.  A monoclonal antibody disrupting calcium-dependent cell-cell adhesion of brain tissues: possible role of its target antigen in animal pattern formation.

Authors:  K Hatta; T S Okada; M Takeichi
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

5.  Cleavage of A-CAM by endogenous proteinases in cultured lens cells and in developing chick embryos.

Authors:  T Volk; T Volberg; I Sabanay; B Geiger
Journal:  Dev Biol       Date:  1990-06       Impact factor: 3.582

6.  ADH-1 suppresses N-cadherin-dependent pancreatic cancer progression.

Authors:  Yasushi Shintani; Yuri Fukumoto; Nina Chaika; Paul M Grandgenett; Michael A Hollingsworth; Margaret J Wheelock; Keith R Johnson
Journal:  Int J Cancer       Date:  2008-01-01       Impact factor: 7.396

Review 7.  Angiogenesis: an organizing principle for drug discovery?

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8.  Targeting N-cadherin enhances antitumor activity of cytotoxic therapies in melanoma treatment.

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Journal:  Cancer Res       Date:  2008-05-15       Impact factor: 12.701

9.  Clinical and pharmacological phase I evaluation of Exherin (ADH-1), a selective anti-N-cadherin peptide in patients with N-cadherin-expressing solid tumours.

Authors:  A Perotti; C Sessa; A Mancuso; C Noberasco; S Cresta; A Locatelli; M L Carcangiu; K Passera; A Braghetti; D Scaramuzza; F Zanaboni; A Fasolo; G Capri; M Miani; W P Peters; L Gianni
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Journal:  PLoS One       Date:  2012-02-15       Impact factor: 3.240

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  19 in total

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2.  Interplay between cadherins and α2β1 integrin differentially regulates melanoma cell invasion.

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Authors:  Y Klymenko; O Kim; E Loughran; J Yang; R Lombard; M Alber; M S Stack
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Review 4.  Complex Determinants of Epithelial: Mesenchymal Phenotypic Plasticity in Ovarian Cancer.

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Review 7.  Cadherin Signaling in Cancer: Its Functions and Role as a Therapeutic Target.

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8.  Molecular and nanoscale evaluation of N-cadherin expression in invasive bladder cancer cells under control conditions or GW501516 exposure.

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Review 9.  N-cadherin in cancer metastasis, its emerging role in haematological malignancies and potential as a therapeutic target in cancer.

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Review 10.  The E-Cadherin and N-Cadherin Switch in Epithelial-to-Mesenchymal Transition: Signaling, Therapeutic Implications, and Challenges.

Authors:  Chin-Yap Loh; Jian Yi Chai; Ting Fang Tang; Won Fen Wong; Gautam Sethi; Muthu Kumaraswamy Shanmugam; Pei Pei Chong; Chung Yeng Looi
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