Literature DB >> 28955112

Vascular Anomalies Caused by Abnormal Signaling within Endothelial Cells: Targets for Novel Therapies.

Ha-Long Nguyen1, Laurence M Boon1,2, Miikka Vikkula1,2.   

Abstract

Vascular anomalies arise as a consequence of improper development and maintenance of the vasculature. Our knowledge on the pathophysiological bases of vascular anomalies has skyrocketed during the past 5 years. It is becoming clear that common intracellular signaling pathways are often activated by mutations, causing endothelial cell dysfunction. These mutations cause hyperactivation of two major intracellular signaling pathways that may be controlled by inhibitors developed for cancer treatment. Although we do not know yet all the downstream effects, it has become evident that normalization of the abnormal signaling is an interesting target for therapy. This is a major paradigm change, as developmental malformations were considered to be inert to any molecular treatment.

Entities:  

Keywords:  interventional radiology; mutations; vascular malformations

Year:  2017        PMID: 28955112      PMCID: PMC5615384          DOI: 10.1055/s-0037-1604296

Source DB:  PubMed          Journal:  Semin Intervent Radiol        ISSN: 0739-9529            Impact factor:   1.513


  51 in total

1.  Rac-MEKK3-MKK3 scaffolding for p38 MAPK activation during hyperosmotic shock.

Authors:  Mark T Uhlik; Amy N Abell; Nancy L Johnson; Weiyong Sun; Bruce D Cuevas; Katherine E Lobel-Rice; Eric A Horne; Mark L Dell'Acqua; Gary L Johnson
Journal:  Nat Cell Biol       Date:  2003-11-23       Impact factor: 28.824

2.  Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ.

Authors:  Matthew D Shirley; Hao Tang; Carol J Gallione; Joseph D Baugher; Laurence P Frelin; Bernard Cohen; Paula E North; Douglas A Marchuk; Anne M Comi; Jonathan Pevsner
Journal:  N Engl J Med       Date:  2013-05-08       Impact factor: 91.245

3.  Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).

Authors:  T Sahoo; E W Johnson; J W Thomas; P M Kuehl; T L Jones; C G Dokken; J W Touchman; C J Gallione; S Q Lee-Lin; B Kosofsky; J H Kurth; D N Louis; G Mettler; L Morrison; A Gil-Nagel; S S Rich; J M Zabramski; M S Boguski; E D Green; D A Marchuk
Journal:  Hum Mol Genet       Date:  1999-11       Impact factor: 6.150

4.  Identification of BMP9 and BMP10 as functional activators of the orphan activin receptor-like kinase 1 (ALK1) in endothelial cells.

Authors:  Laurent David; Christine Mallet; Sabine Mazerbourg; Jean-Jacques Feige; Sabine Bailly
Journal:  Blood       Date:  2006-10-26       Impact factor: 22.113

5.  A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7.

Authors:  Pinar Bayrak-Toydemir; Jamie McDonald; Nurten Akarsu; Reha M Toydemir; Fernanda Calderon; Timur Tuncali; Wei Tang; Franklin Miller; Rong Mao
Journal:  Am J Med Genet A       Date:  2006-10-15       Impact factor: 2.802

6.  Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome.

Authors:  Kyle C Kurek; Valerie L Luks; Ugur M Ayturk; Ahmad I Alomari; Steven J Fishman; Samantha A Spencer; John B Mulliken; Margot E Bowen; Guilherme L Yamamoto; Harry P W Kozakewich; Matthew L Warman
Journal:  Am J Hum Genet       Date:  2012-05-31       Impact factor: 11.025

7.  Biallelic somatic and germline mutations in cerebral cavernous malformations (CCMs): evidence for a two-hit mechanism of CCM pathogenesis.

Authors:  Amy L Akers; Eric Johnson; Gary K Steinberg; Joseph M Zabramski; Douglas A Marchuk
Journal:  Hum Mol Genet       Date:  2008-12-16       Impact factor: 6.150

8.  Somatic Activating PIK3CA Mutations Cause Venous Malformation.

Authors:  Nisha Limaye; Jaakko Kangas; Antonella Mendola; Catherine Godfraind; Matthieu J Schlögel; Raphael Helaers; Lauri Eklund; Laurence M Boon; Miikka Vikkula
Journal:  Am J Hum Genet       Date:  2015-12-03       Impact factor: 11.025

9.  PIK3CA activating mutations in facial infiltrating lipomatosis.

Authors:  Reid A Maclellan; Valerie L Luks; Matthew P Vivero; John B Mulliken; David Zurakowski; Bonnie L Padwa; Matthew L Warman; Arin K Greene; Kyle C Kurek
Journal:  Plast Reconstr Surg       Date:  2014-01       Impact factor: 4.730

10.  BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia.

Authors:  Whitney L Wooderchak-Donahue; Jamie McDonald; Brendan O'Fallon; Paul D Upton; Wei Li; Beth L Roman; Sarah Young; Parker Plant; Gyula T Fülöp; Carmen Langa; Nicholas W Morrell; Luisa M Botella; Carmelo Bernabeu; David A Stevenson; James R Runo; Pinar Bayrak-Toydemir
Journal:  Am J Hum Genet       Date:  2013-08-22       Impact factor: 11.025

View more
  7 in total

Review 1.  New and Emerging Targeted Therapies for Vascular Malformations.

Authors:  An Van Damme; Emmanuel Seront; Valérie Dekeuleneer; Laurence M Boon; Miikka Vikkula
Journal:  Am J Clin Dermatol       Date:  2020-10       Impact factor: 7.403

2.  Endothelial GNAQ p.R183Q Increases ANGPT2 (Angiopoietin-2) and Drives Formation of Enlarged Blood Vessels.

Authors:  Lan Huang; Colette Bichsel; Alexis L Norris; Jeremy Thorpe; Jonathan Pevsner; Sanda Alexandrescu; Anna Pinto; David Zurakowski; Robin J Kleiman; Mustafa Sahin; Arin K Greene; Joyce Bischoff
Journal:  Arterioscler Thromb Vasc Biol       Date:  2021-10-21       Impact factor: 8.311

3.  Gorham-Stout case report: a multi-omic analysis reveals recurrent fusions as new potential drivers of the disease.

Authors:  Marcos Yébenes Mayordomo; Sofian Al Shboul; Maria Gómez-Herranz; Asim Azfer; Alison Meynert; Donald Salter; Larry Hayward; Anca Oniscu; James T Patton; Ted Hupp; Mark J Arends; Javier Antonio Alfaro
Journal:  BMC Med Genomics       Date:  2022-06-06       Impact factor: 3.622

Review 4.  Endothelial sprouting, proliferation, or senescence: tipping the balance from physiology to pathology.

Authors:  Severin Mühleder; Macarena Fernández-Chacón; Irene Garcia-Gonzalez; Rui Benedito
Journal:  Cell Mol Life Sci       Date:  2020-10-19       Impact factor: 9.261

Review 5.  A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestations.

Authors:  Guillaume Canaud; Adrienne M Hammill; Denise Adams; Miikka Vikkula; Kim M Keppler-Noreuil
Journal:  Orphanet J Rare Dis       Date:  2021-07-08       Impact factor: 4.123

Review 6.  A Primer on a Comprehensive Genetic Approach to Vascular Anomalies.

Authors:  Alexandra J Borst; Taizo A Nakano; Francine Blei; Denise M Adams; Jessica Duis
Journal:  Front Pediatr       Date:  2020-10-19       Impact factor: 3.418

7.  Efficacy and safety of sirolimus in the treatment of vascular malformations: A protocol for systematic review and meta-analysis.

Authors:  Jianyong Dong; Deting Han; Desheng Wang; Huijun Lu; Xiaoliang Wang
Journal:  Medicine (Baltimore)       Date:  2020-10-02       Impact factor: 1.817

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.