Literature DB >> 12139711

The effect of keratinocyte growth factor on healing of manifest radiation ulcers in mouse tongue epithelium.

W Dörr1, K Spekl, C L Farrell.   

Abstract

The purpose of this study was to examine the effect of recombinant human keratinocyte growth factor (rHuKGF) on clinically manifest acute oral mucositis. The animal model utilized in this investigation was ventral tongue epithelium of C3H/Neu mice. In a first experiment, graded single doses were applied in order to define dose effect and time course of acute mucosal ulceration, as a clinically relevant endpoint. Irradiation was given to a 3 x 3 mm2 test field in the centre of the ventral tongue with 25 kV X-rays. A single dose of 18 Gy, i.e. a dose after which ulceration is expected in more than 99% of the animals, was applied in subsequent experiments. In the study group of 20 animals, rHuKGF was applied at a daily dose of 5 mg/kg subcutaneously from the time of first diagnosis of ulcer for a maximum of 5 days. In the control group, phosphate-buffered saline was used as a placebo. The time course of ulceration, i.e. individual ulcer duration, was analysed in both the control group without rHuKGF and the study group. Irradiation with graded single doses yielded an ED50 of 11.5 +/- 0.7 Gy (logit analysis). In responding animals, the latent time to first diagnosis of ulceration and the individual ulcer duration were independent of dose. Mean latency (+/- standard deviation) was 10.5 +/- 0.5 days, mean ulcer duration 3.9 +/- 0.6 days for doses 11, 13 and 16 Gy. After a dose of 18 Gy, 39 animals developed ulceration after a mean latency of 9.3 +/- 0.3 days (control and KGF-treated). The average ulcer duration was 4.2 +/- 0.9 days in the placebo group and 4.8 +/- 0.8 days in the KGF group (P = 0.02). We conclude that when rHuKGF treatment is delayed until radiation-induced ulcers are manifest, the therapeutic activity previously reported with other treatment schedules was not observed and there was a slight prolongation of duration of ulceration. These data suggest that during tumour radiotherapy, effective rHuKGF therapy schedules should include administration before the onset of ulcerative mucositis.

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Year:  2002        PMID: 12139711      PMCID: PMC6496397          DOI: 10.1046/j.1365-2184.35.s1.9.x

Source DB:  PubMed          Journal:  Cell Prolif        ISSN: 0960-7722            Impact factor:   6.831


  22 in total

1.  Changes in keratinocyte differentiation during accelerated repopulation of the irradiated mouse epidermis.

Authors:  K Liu; M Kasper; K R Trott
Journal:  Int J Radiat Biol       Date:  1996-06       Impact factor: 2.694

Review 2.  [The therapeutic management of radiogenic oral mucositis].

Authors:  W Dörr; I Dölling-Jochem; M Baumann; T Herrmann
Journal:  Strahlenther Onkol       Date:  1997-04       Impact factor: 3.621

3.  Effect of changing weekly dose on accelerated repopulation during fractionated irradiation of mouse tongue mucosa.

Authors:  W Dörr; M Weber-Frisch
Journal:  Int J Radiat Biol       Date:  1995-05       Impact factor: 2.694

4.  Prevention of chemotherapy-induced ulcerative mucositis by transforming growth factor beta 3.

Authors:  S T Sonis; L Lindquist; A Van Vugt; A A Stewart; K Stam; G Y Qu; K K Iwata; J D Haley
Journal:  Cancer Res       Date:  1994-03-01       Impact factor: 12.701

5.  Modification of oral mucositis by keratinocyte growth factor: single radiation exposure.

Authors:  W Dörr; R Noack; K Spekl; C L Farrell
Journal:  Int J Radiat Biol       Date:  2001-03       Impact factor: 2.694

6.  Short-term immobilization of mice by methohexitone.

Authors:  W Dörr; M Weber-Frisch
Journal:  Lab Anim       Date:  1999-01       Impact factor: 2.471

7.  Repopulation in mouse oral mucosa: changes in the effect of dose fractionation.

Authors:  W Dörr; K Brankovic; B Hartmann
Journal:  Int J Radiat Biol       Date:  2000-03       Impact factor: 2.694

8.  Stimulation and inhibition of proliferation in the small intestinal crypts of the mouse after in vivo administration of growth factors.

Authors:  C S Potten; G Owen; D Hewitt; C A Chadwick; H Hendry; B I Lord; L B Woolford
Journal:  Gut       Date:  1995-06       Impact factor: 23.059

9.  Interleukin 1 increases thymidine labeling index of normal tissues of mice but not the tumor.

Authors:  M S Zaghloul; M J Dorie; R F Kallman
Journal:  Int J Radiat Oncol Biol Phys       Date:  1994-07-01       Impact factor: 7.038

10.  Human keratinocyte growth factor effects in a porcine model of epidermal wound healing.

Authors:  L Staiano-Coico; J G Krueger; J S Rubin; S D'limi; V P Vallat; L Valentino; T Fahey; A Hawes; G Kingston; M R Madden
Journal:  J Exp Med       Date:  1993-09-01       Impact factor: 14.307

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  13 in total

1.  Epithelial separation theory for post-tonsillectomy secondary hemorrhage: evidence in a mouse model and potential heparin-binding epidermal growth factor-like growth factor therapy.

Authors:  Daniel M Beswick; Chloe Santa Maria; Noel F Ayoub; Robson Capasso; Peter Luke Santa Maria
Journal:  Eur Arch Otorhinolaryngol       Date:  2017-11-29       Impact factor: 2.503

Review 2.  Growth factors and cytokines in the prevention and treatment of oral and gastrointestinal mucositis.

Authors:  Inger von Bültzingslöwen; Michael T Brennan; Fred K L Spijkervet; Richard Logan; Andrea Stringer; Judith E Raber-Durlacher; Dorothy Keefe
Journal:  Support Care Cancer       Date:  2006-04-21       Impact factor: 3.603

3.  Effect of post-exposure administration of keratinocyte growth factor (Palifermin) on radiation effects in oral mucosa in mice.

Authors:  Yasemin Kiliç; Katja Rajewski; Wolfgang Dörr
Journal:  Radiat Environ Biophys       Date:  2006-11-14       Impact factor: 1.925

4.  Durability of and role of AKT in FGF7p urothelial protection against cyclophosphamide.

Authors:  Sridhar Tatarao Narla; Lori Rice; David Ostrov; Daniel Scott Bushnell; Joanne Lindsey Duara; Carlton Matthew Bates
Journal:  Physiol Rep       Date:  2022-06

5.  Effect of tumour-cell-derived or recombinant keratinocyte growth factor (KGF) on proliferation and radioresponse of human epithelial tumour cells (HNSCC) and normal keratinocytes in vitro.

Authors:  Andrea Hille; Susanne Grüger; Hans Christiansen; Hendrik A Wolff; Beate Volkmer; Jörg Lehmann; Wolfgang Dörr; Margret Rave-Fränk
Journal:  Radiat Environ Biophys       Date:  2010-03-07       Impact factor: 1.925

6.  Cell kinetic studies in the murine ventral tongue epithelium: the effects of repeated exposure to keratinocyte growth factor.

Authors:  C S Potten; D Booth; N J Cragg; J A O'Shea; G L Tudor; C Booth
Journal:  Cell Prolif       Date:  2002-08       Impact factor: 6.831

7.  Prevention of radiation-induced oral mucositis after adenoviral vector-mediated transfer of the keratinocyte growth factor cDNA to mouse submandibular glands.

Authors:  Changyu Zheng; Ana P Cotrim; Abraham N Sunshine; Takayuki Sugito; Lina Liu; Anastasia Sowers; James B Mitchell; Bruce J Baum
Journal:  Clin Cancer Res       Date:  2009-07-07       Impact factor: 12.531

8.  AKT Signaling Downstream of KGF Is Necessary and Sufficient for Blocking Cyclophosphamide Bladder Injury.

Authors:  Sridhar T Narla; Daniel S Bushnell; Joanne L Duara; Carlton M Bates
Journal:  Am J Pathol       Date:  2022-01-19       Impact factor: 5.770

9.  Protected graft copolymer-formulated fibroblast growth factors mitigate the lethality of partial body irradiation injury.

Authors:  Gerardo M Castillo; Akiko Nishimoto-Ashfield; Cynthia C Jones; Kasim K Kabirov; Alexander Zakharov; Alexander V Lyubimov
Journal:  PLoS One       Date:  2017-02-16       Impact factor: 3.240

10.  Palifermin for management of treatment-induced oral mucositis in cancer patients.

Authors:  Andrei Barasch; Joel Epstein; Ken Tilashalski
Journal:  Biologics       Date:  2009-07-13
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