Literature DB >> 21333567

Masitinib as a chemosensitizer of canine tumor cell lines: a proof of concept study.

D H Thamm1, B Rose, K Kow, M Humbert, C D Mansfield, A Moussy, O Hermine, P Dubreuil.   

Abstract

Masitinib, a selective tyrosine kinase inhibitor, has previously been shown to enhance the antiproliferative effects of gemcitabine in human pancreatic cancer, demonstrating potential as a chemosensitizer. This exploratory study investigated the ability of masitinib to sensitize various canine cancer cell lines to doxorubicin, vinblastine, and gemcitabine. Masitinib strongly sensitized histiocytic sarcoma cells to vinblastine (>70-fold reduction in IC(50) at 5 μM masitinib), as well as osteosarcoma and mammary carcinoma cells to gemcitabine (>70-fold reduction at 5-10 μM). In addition, several cell lines were sensitized to doxorubicin (2-10-fold reduction at 10 μM). These data establish proof-of-concept that masitinib in combination with chemotherapeutic agents can generate synergistic growth inhibition in various canine cancers, possibly through chemosensitization. The findings justify further investigation into those combinations that may potentially yield therapeutic benefit.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21333567     DOI: 10.1016/j.tvjl.2011.01.001

Source DB:  PubMed          Journal:  Vet J        ISSN: 1090-0233            Impact factor:   2.688


  9 in total

1.  Detection of novel polymorphisms in the ckit gene of canine patients with lymphoma, melanoma, haemangiosarcoma, and osteosarcoma.

Authors:  Irina Gramer; Martin Kessler; Joachim Geyer
Journal:  Vet Res Commun       Date:  2016-03-12       Impact factor: 2.459

2.  Presumed masitinib-induced nephrotic syndrome and azotemia in a dog.

Authors:  Lauren Devine; David J Polzin
Journal:  Can Vet J       Date:  2016-07       Impact factor: 1.008

3.  Transcriptome and proteome analysis of tyrosine kinase inhibitor treated canine mast cell tumour cells identifies potentially kit signaling-dependent genes.

Authors:  Robert Klopfleisch; Anja Meyer; Patricia Schlieben; Angelika Bondzio; Chris Weise; Dido Lenze; Michael Hummel; Ralf Einspanier; Achim D Gruber
Journal:  BMC Vet Res       Date:  2012-06-29       Impact factor: 2.741

4.  Evaluation of the drug sensitivity and expression of 16 drug resistance-related genes in canine histiocytic sarcoma cell lines.

Authors:  Hajime Asada; Hirotaka Tomiyasu; Yuko Goto-Koshino; Yasuhito Fujino; Koichi Ohno; Hajime Tsujimoto
Journal:  J Vet Med Sci       Date:  2015-02-21       Impact factor: 1.267

Review 5.  Mechanisms of Drug Resistance in Veterinary Oncology- A Review with an Emphasis on Canine Lymphoma.

Authors:  Maurice Zandvliet; Erik Teske
Journal:  Vet Sci       Date:  2015-08-12

6.  A novel canine histiocytic sarcoma cell line: initial characterization and utilization for drug screening studies.

Authors:  Marilia Takada; Maciej Parys; Emmalena Gregory-Bryson; Paulo Vilar Saavedra; Matti Kiupel; Vilma Yuzbasiyan-Gurkan
Journal:  BMC Cancer       Date:  2018-03-01       Impact factor: 4.430

7.  Cyclooxygenase inhibitors potentiate receptor tyrosine kinase therapies in bladder cancer cells in vitro.

Authors:  Jennifer Bourn; Maria Cekanova
Journal:  Drug Des Devel Ther       Date:  2018-06-13       Impact factor: 4.162

8.  Effects of Tyrosine Kinase Inhibitor-masitinib Mesylate on Canine Mammary Tumour Cell Lines.

Authors:  Fulya Ustun-Alkan; Tülay Bakırel; Oya Üstüner; Ceren Anlas; Suzan Cinar; Funda Yıldırım; Aydın Gürel
Journal:  J Vet Res       Date:  2021-07-24       Impact factor: 1.744

9.  Antiproliferative effects of masitinib and imatinib against canine oral fibrosarcoma in vitro.

Authors:  Milan Milovancev; Stuart C Helfand; Kevin Marley; Cheri P Goodall; Christiane V Löhr; Shay Bracha
Journal:  BMC Vet Res       Date:  2016-06-04       Impact factor: 2.741

  9 in total

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