Literature DB >> 20364346

The effects of methylprednisolone and halofuginone on preventing esophageal and hypopharyngeal fibrosis in delivered radiotherapy.

Hakan Dabak1, Turgut Karlidag, Nusret Akpolat, Erol Keles, Hayrettin Cengiz Alpay, Meltem Serin, Irfan Kaygusuz, Sinasi Yalcin, Ozgur Isik.   

Abstract

In this study, we assessed the effects of halofuginone and methylprednisolone on hypopharyngeal and esophageal stricture that can develop following radiation to the head and neck of rats. Rats were divided into four groups randomly and 18 Gy radiation was given to the head and neck regions of all rats except the control group. Group 1 (Control Group): No radiation or drugs were administered. Group 2 (Radiation Group): only radiation was applied without any drugs. Group 3 (Halofuginone Group): halofuginone 100 microg/kg per day was given intraperitoneally. Group 4 (Methylprednisolone Group): methylprednisolone 1 mg/kg per day was administered intramuscularly. In all groups, 90 days after application of radiation, sections of the proximal esophagus and hypopharynx were examined for fibrosis, fibroblast proliferation, vascularization, epithelial atypia, necrosis, polymorphonuclear leukocytes, mononuclear cells, and stenosis index by light microscope and the hydroxyproline levels were assessed biochemically. Fibrosis, epithelial atypia and hydroxyproline levels were found to be significantly higher in the radiation group compared to the control group (P < 0.05). We did not observe fibrosis in either the halofuginone or the control groups. Fibrosis was also significantly lower in the methylprednisolone group than the radiation group (P < 0.05). The differences of the stenosis index scores between the groups were not statistically significant (P < 0.05). Vascularization was similar in all groups. We think that especially halofuginone is a drug that can be used safely to prevent fibrosis due to radiotherapy, but further studies are needed.

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Year:  2010        PMID: 20364346     DOI: 10.1007/s00405-010-1242-y

Source DB:  PubMed          Journal:  Eur Arch Otorhinolaryngol        ISSN: 0937-4477            Impact factor:   2.503


  24 in total

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Authors:  E Eylem Ertuğrul; Hakan Cincik; Salim Dogru; Engin Cekin; Ufuk Berber; Atila Gungor; I Ethem Poyrazoğlu
Journal:  Laryngoscope       Date:  2007-02       Impact factor: 3.325

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Authors:  R Bruck; O Genina; H Aeed; R Alexiev; A Nagler; Y Avni; M Pines
Journal:  Hepatology       Date:  2001-02       Impact factor: 17.425

5.  Halofuginone, an inhibitor of type-I collagen synthesis and skin sclerosis, blocks transforming-growth-factor-beta-mediated Smad3 activation in fibroblasts.

Authors:  Tracy L McGaha; Robert G Phelps; Harry Spiera; Constantin Bona
Journal:  J Invest Dermatol       Date:  2002-03       Impact factor: 8.551

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Journal:  J Biol Chem       Date:  2004-01-19       Impact factor: 5.157

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Journal:  Radiology       Date:  1983-08       Impact factor: 11.105

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  3 in total

Review 1.  Halofuginone for fibrosis, regeneration and cancer in the gastrointestinal tract.

Authors:  Mark Pines
Journal:  World J Gastroenterol       Date:  2014-10-28       Impact factor: 5.742

2.  Preliminary results of antiscarring therapy in the prevention of postendoscopic esophageal mucosectomy strictures.

Authors:  Yuhsin Wu; Steve J Schomisch; Cassandra Cipriano; Amitabh Chak; Richard H Lash; Jeffrey L Ponsky; Jeffrey M Marks
Journal:  Surg Endosc       Date:  2013-10-08       Impact factor: 4.584

3.  Inhibition of TGF-β signaling with halofuginone can enhance the antitumor effect of irradiation in Lewis lung cancer.

Authors:  Runlong Lin; Shuai Yi; Linlin Gong; Weishuai Liu; Peng Wang; Ningbo Liu; Lujun Zhao; Ping Wang
Journal:  Onco Targets Ther       Date:  2015-12-02       Impact factor: 4.147

  3 in total

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