Literature DB >> 20846006

Adrenomedullin as a therapeutic target in angiogenesis.

Jean-Laurent Deville1, Sébastien Salas, Dominique Figarella-Branger, L'Houcine Ouafik, Laurent Daniel.   

Abstract

IMPORTANCE OF THE FIELD: Hypoxia, a frequent characteristic in the microenvironment of solid tumors, leads to adrenomedullin (AM) upregulation through the hypoxia inducible factor-1 pathway, explaining its high expression in a variety of malignant tissues. AM is believed to play an important role in tumor progression and angiogenesis in many cancers. Therefore, it could become a new therapeutic target. AREAS COVERED IN THIS REVIEW: We performed a review of the literature based on published data to highlight AM's critical roles in tumor cell growth and cancer invasiveness, and its involvement in tumor angiogenesis through promotion of recruitment of hematopoietic progenitors, vascular morphogenesis, and blood vessel stabilization and maturation. Inhibition of AM has antitumoral effects linked to antiangiogenic effects but in some cases also to direct antiproliferative activity on cancer cells. Several studies demonstrated that systemic inhibition of AM receptors was well tolerated in murine models. WHAT THE READER WILL GAIN: The goal of this review is to inform readers about the role of AM in tumor angiogenesis and cancer progression and, therefore, about its possible place as a new therapeutic target. TAKE HOME MESSAGE: Taken together, these data support targeting the AM pathway as a new potential therapy in cancer, complementary to other existing treatments.

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Year:  2010        PMID: 20846006     DOI: 10.1517/14728222.2010.522328

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  6 in total

1.  Effects of nickel treatment on H3K4 trimethylation and gene expression.

Authors:  Kam-Meng Tchou-Wong; Kathrin Kiok; Zuojian Tang; Thomas Kluz; Adriana Arita; Phillip R Smith; Stuart Brown; Max Costa
Journal:  PLoS One       Date:  2011-03-24       Impact factor: 3.240

2.  Lack of adrenomedullin in mouse endothelial cells results in defective angiogenesis, enhanced vascular permeability, less metastasis, and more brain damage.

Authors:  Laura Ochoa-Callejero; Andrea Pozo-Rodrigálvarez; Ricardo Martínez-Murillo; Alfredo Martínez
Journal:  Sci Rep       Date:  2016-09-19       Impact factor: 4.379

3.  Infiltrating mast cells promote renal cell carcinoma angiogenesis by modulating PI3K→︀AKT→︀GSK3β→︀AM signaling.

Authors:  Y Chen; C Li; H Xie; Y Fan; Z Yang; J Ma; D He; L Li
Journal:  Oncogene       Date:  2017-01-23       Impact factor: 9.867

4.  Development of chimeric and bifunctional antagonists for CLR/RAMP receptors.

Authors:  Chia Lin Chang; Sheau Yu Teddy Hsu
Journal:  PLoS One       Date:  2019-05-31       Impact factor: 3.240

5.  AR facilitates YAP-TEAD interaction with the AM promoter to enhance mast cell infiltration into cutaneous neurofibroma.

Authors:  Jing Jia; Haibao Zhang; Hongke Zhang; Wenbo Liu; Huicong Du; Maoguo Shu; Lin He
Journal:  Sci Rep       Date:  2019-12-18       Impact factor: 4.379

6.  PERK-mediated expression of peptidylglycine α-amidating monooxygenase supports angiogenesis in glioblastoma.

Authors:  Himanshu Soni; Julia Bode; Chi D L Nguyen; Laura Puccio; Michelle Neßling; Rosario M Piro; Jonas Bub; Emma Phillips; Robert Ahrends; Betty A Eipper; Björn Tews; Violaine Goidts
Journal:  Oncogenesis       Date:  2020-02-13       Impact factor: 7.485

  6 in total

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