Literature DB >> 10680582

Treatment and survival study in the C57BL/6J-APC(Min)/+(Min) mouse with R-flurbiprofen.

W J Wechter1, E D Murray, D Kantoci, D D Quiggle, D D Leipold, K M Gibson, J D McCracken.   

Abstract

Our previous studies with the mouse model of familial adenomatous polyposis (FAP), C57BL/6J-APC(Min)/+ or Min mouse, demonstrated the optimal dose for adenoma reduction with R-flurbiprofen was 10 mg/kg/day as an undivided dose. Divided doses exhibited no increased efficaciousness. This study examines 10 mg/kg R-flurbiprofen daily (qd) on survival as well as a second daily (q.o.d.) schedule and compares it with sulindac sulfone. The q.o.d. schedule at 10 mg/kg was equally efficacious as qd treatment at the same dose. For the q.o.d. group, tumor number decreased similarly (p<0.01); while body weight gain (p<0.01), hematocrit and average tumor area (both, p<0.05) were improved compared with qd treatment. Treatment with R-flurbiprofen (10 mg/kg/day) increased survival significantly (p=0.0004, log-rank) compared to vehicle treated animals. Major biological endpoints (hematocrit, weight gain, tumor number, average and total area [99% reduction]) were significantly improved in treated animals (p<0.01). Sulindac sulfone treatment (50 mg/kg/day) of the Min mouse produced no significant biological benefit. The dose schedule study suggests that for tumor reduction it is necessary to attain a threshold drug-level but not necessarily sustain it over 24 hrs (pharmacodynamic t1/2 >> pharmacokinetic t1/2). During the period of administration R-flurbiprofen dramatically prolongs survival for the mouse model of the human disease, FAP.

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Year:  2000        PMID: 10680582     DOI: 10.1016/s0024-3205(99)00645-1

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  7 in total

1.  R-flurbiprofen, a novel nonsteroidal anti-inflammatory drug, decreases cell proliferation and induces apoptosis in pituitary adenoma cells in vitro.

Authors:  James K Liu; Smruti K Patel; David L Gillespie; Kum Whang; William T Couldwell
Journal:  J Neurooncol       Date:  2011-09-22       Impact factor: 4.130

2.  NSAIDs and enantiomers of flurbiprofen target gamma-secretase and lower Abeta 42 in vivo.

Authors:  Jason L Eriksen; Sarah A Sagi; Tawnya E Smith; Sascha Weggen; Pritam Das; D C McLendon; Victor V Ozols; Kevin W Jessing; Kenton H Zavitz; Edward H Koo; Todd E Golde
Journal:  J Clin Invest       Date:  2003-08       Impact factor: 14.808

3.  Insulin receptor substrate-1 deficiency promotes apoptosis in the putative intestinal crypt stem cell region, limits Apcmin/+ tumors, and regulates Sox9.

Authors:  Nicole M Ramocki; Heather R Wilkins; Scott T Magness; James G Simmons; Brooks P Scull; Ginny H Lee; Kirk K McNaughton; P Kay Lund
Journal:  Endocrinology       Date:  2007-10-04       Impact factor: 4.736

Review 4.  Point: From animal models to prevention of colon cancer. Systematic review of chemoprevention in min mice and choice of the model system.

Authors:  Denis E Corpet; Fabrice Pierre
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2003-05       Impact factor: 4.254

Review 5.  What are the best routes to effectively model human colorectal cancer?

Authors:  Madeleine Young; Liliana Ordonez; Alan R Clarke
Journal:  Mol Oncol       Date:  2013-02-20       Impact factor: 6.603

Review 6.  Resveratrol and cancer: focus on in vivo evidence.

Authors:  Lindsay G Carter; John A D'Orazio; Kevin J Pearson
Journal:  Endocr Relat Cancer       Date:  2014-05-06       Impact factor: 5.678

7.  R-Flurbiprofen Traps Prostaglandins within Cells by Inhibition of Multidrug Resistance-Associated Protein-4.

Authors:  Ivonne Wobst; Lisa Ebert; Kerstin Birod; Marthe-Susanna Wegner; Marika Hoffmann; Dominique Thomas; Carlo Angioni; Michael J Parnham; Dieter Steinhilber; Irmgard Tegeder; Gerd Geisslinger; Sabine Grösch
Journal:  Int J Mol Sci       Date:  2016-12-30       Impact factor: 5.923

  7 in total

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