Literature DB >> 28339142

Selective effects of oral antiangiogenic tyrosine kinase inhibitors on an animal model of hereditary hemorrhagic telangiectasia.

Y H Kim1, M-J Kim2,3, S-W Choe1,4, D Sprecher5, Y J Lee3, S P Oh1,5.   

Abstract

Essentials Antiangiogenic drugs are indicated as therapies for hereditary hemorrhagic telangiectasia. We interrogated the response to four antiangiogenic drugs for anemia and intestinal bleeding. Sorafenib and a pazopanib analog significantly improved while erlotinib worsened anemia. Some oral antiangiogenic drugs were effective in reducing intestinal bleeding.
SUMMARY: Background Epistaxis and gastrointestinal (GI) tract hemorrhages are common symptoms of aged hereditary hemorrhagic telangiectasia (HHT) patients that result in anemia. Clinical as well as animal studies have suggested that vascular endothelial growth factor (VEGF) neutralizing antibodies lessen hemorrhage associated with adult-onset arteriovenous malformations (AVMs). Objectives The goal of this study is to evaluate potential therapeutic effects of oral delivery of four antiangiogenic tyrosine-kinase inhibitors (TKIs) in the development of adult-onset AVMs in a murine model of HHT. Methods An adult activin receptor-like kinase 1 (Alk1)-inducible knockout (iKO) model was utilized to evaluate the effect of oral administration of sorafenib, sunitinib, erlotinib and a pazopanib analog (GW771806) on hemoglobin level, GI hemorrhages and formation of wound-induced skin AVMs. Results and Conclusions Sorafenib and GW771806 significantly improved, yet erlotinib worsened, anemia and GI-bleeding in the Alk1-iKO model. However, none of these TKIs appeared to be effective for inhibiting the development of wound-induced skin AVMs. Taken together, these results suggest that oral delivery of antiangiogenic TKIs is selectively more effective for GI bleeding than mucocutaneous AVMs, and it may provide an experimental basis for selective therapeutic options depending on the symptoms of HHT.
© 2017 International Society on Thrombosis and Haemostasis.

Entities:  

Keywords:  activin receptors; anemia; angiogenesis inhibitors; arteriovenous malformation; hereditary hemorrhagic; telangiectasia

Mesh:

Substances:

Year:  2017        PMID: 28339142      PMCID: PMC5902312          DOI: 10.1111/jth.13683

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  27 in total

1.  Epidemiological investigation of Rendu-Osler disease in France: its geographical distribution and prevalence.

Authors:  A Bideau; H Plauchu; G Brunet; J Robert
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2.  Antitumor activity of erlotinib in combination with capecitabine in human tumor xenograft models.

Authors:  Kaori F Ouchi; Mieko Yanagisawa; Fumiko Sekiguchi; Yutaka Tanaka
Journal:  Cancer Chemother Pharmacol       Date:  2005-12-16       Impact factor: 3.333

Review 3.  Sorafenib for the treatment of advanced renal cell carcinoma.

Authors:  Robert C Kane; Ann T Farrell; Haleh Saber; Shenghui Tang; Gene Williams; Josephine M Jee; Chengyi Liang; Brian Booth; Nallaperumal Chidambaram; David Morse; Rajeshwari Sridhara; Patricia Garvey; Robert Justice; Richard Pazdur
Journal:  Clin Cancer Res       Date:  2006-12-15       Impact factor: 12.531

4.  Effect of Bevacizumab Nasal Spray on Epistaxis Duration in Hereditary Hemorrhagic Telangectasia: A Randomized Clinical Trial.

Authors:  Sophie Dupuis-Girod; Alexis Ambrun; Evelyne Decullier; Anne-Emmanuelle Fargeton; Adeline Roux; Valentine Bréant; Bettina Colombet; Sophie Rivière; César Cartier; Pascal Lacombe; Thierry Chinet; Sandra Blivet; Jean-Hugues Blondel; Brigitte Gilbert-Dussardier; Xavier Dufour; Justin Michel; Jean-Robert Harle; Patrick Dessi; Frédéric Faure
Journal:  JAMA       Date:  2016-09-06       Impact factor: 56.272

5.  Effect of Topical Intranasal Therapy on Epistaxis Frequency in Patients With Hereditary Hemorrhagic Telangiectasia: A Randomized Clinical Trial.

Authors:  Kevin J Whitehead; Nathan B Sautter; Justin P McWilliams; Murali M Chakinala; Christian A Merlo; Maribeth H Johnson; Melissa James; Eric M Everett; Marianne S Clancy; Marie E Faughnan; S Paul Oh; Scott E Olitsky; Reed E Pyeritz; James R Gossage
Journal:  JAMA       Date:  2016-09-06       Impact factor: 56.272

Review 6.  Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease.

Authors:  S A Abdalla; M Letarte
Journal:  J Med Genet       Date:  2005-05-06       Impact factor: 6.318

Review 7.  Pazopanib: the newest tyrosine kinase inhibitor for the treatment of advanced or metastatic renal cell carcinoma.

Authors:  Sidney V Keisner; Sachin R Shah
Journal:  Drugs       Date:  2011-03-05       Impact factor: 9.546

8.  Bevacizumab reverses need for liver transplantation in hereditary hemorrhagic telangiectasia.

Authors:  Andrew Mitchell; Leon A Adams; Gerry MacQuillan; Jon Tibballs; Rohan vanden Driesen; Luc Delriviere
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Review 9.  Molecular basis for sunitinib efficacy and future clinical development.

Authors:  Sandrine Faivre; George Demetri; William Sargent; Eric Raymond
Journal:  Nat Rev Drug Discov       Date:  2007-09       Impact factor: 84.694

10.  Common and distinctive pathogenetic features of arteriovenous malformations in hereditary hemorrhagic telangiectasia 1 and hereditary hemorrhagic telangiectasia 2 animal models--brief report.

Authors:  Eva M Garrido-Martin; Ha-Long Nguyen; Tyler A Cunningham; Se-Woon Choe; Zhihua Jiang; Helen M Arthur; Young-Jae Lee; S Paul Oh
Journal:  Arterioscler Thromb Vasc Biol       Date:  2014-07-31       Impact factor: 8.311

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Review 2.  Hereditary hemorrhagic telangiectasia: diagnosis and management from the hematologist's perspective.

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Journal:  Haematologica       Date:  2018-05-24       Impact factor: 9.941

3.  Pazopanib may reduce bleeding in hereditary hemorrhagic telangiectasia.

Authors:  Marie E Faughnan; James R Gossage; Murali M Chakinala; S Paul Oh; Raj Kasthuri; Christopher C W Hughes; Justin P McWilliams; Joseph G Parambil; Nicholas Vozoris; Jill Donaldson; Gitanjali Paul; Pamela Berry; Dennis L Sprecher
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4.  SMAD4 Deficiency Leads to Development of Arteriovenous Malformations in Neonatal and Adult Mice.

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Review 5.  Future treatments for hereditary hemorrhagic telangiectasia.

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Review 6.  Hereditary Haemorrhagic Telangiectasia, an Inherited Vascular Disorder in Need of Improved Evidence-Based Pharmaceutical Interventions.

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Review 7.  Hereditary Hemorrhagic Telangiectasia: Genetics, Pathophysiology, Diagnosis, and Management.

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8.  Overexpression of Activin Receptor-Like Kinase 1 in Endothelial Cells Suppresses Development of Arteriovenous Malformations in Mouse Models of Hereditary Hemorrhagic Telangiectasia.

Authors:  Yong Hwan Kim; Phuong-Nhung Vu; Se-Woon Choe; Chang-Jin Jeon; Helen M Arthur; Calvin P H Vary; Young Jae Lee; S Paul Oh
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9.  Defective Flow-Migration Coupling Causes Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia.

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10.  Pazopanib for severe bleeding and transfusion-dependent anemia in hereditary hemorrhagic telangiectasia.

Authors:  Joseph G Parambil; James R Gossage; Keith R McCrae; Troy D Woodard; K V Narayanan Menon; Kasi L Timmerman; Douglas P Pederson; Dennis L Sprecher; Hanny Al-Samkari
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