Literature DB >> 15247138

Irreversible ototoxicity associated with difluoromethylornithine.

Christopher D Lao1, Patricia Backoff, Lawrence I Shotland, Deborah McCarty, Tracy Eaton, Frank G Ondrey, Jaye L Viner, Stuart Jon Spechler, Ernest T Hawk, Dean E Brenner.   

Abstract

Difluoromethylornithine (DFMO) is a potent, irreversible inhibitor of ornithine decarboxylase, the rate-limiting enzyme in the synthesis of polyamines that promote cellular proliferation. DFMO has been tested as a potential cancer therapeutic and chemopreventive agent in clinical trials. Reversible hearing loss is a recognized toxicity of DFMO that usually occurs at doses above 2 g/m(2)/d, and generally when the cumulative dose exceeds 250 g/m(2). In a recently completed Barrett's esophagus chemoprevention trial, a participant developed a 15-dB decrease in hearing at frequencies of 250, 2,000, and 3,000 Hz in the right ear and a > or =20-dB decrease in hearing at 4,000 to 6,000 Hz in the left ear after taking 0.5 g/m(2)/d DFMO for approximately 13 weeks (cumulative dose of 45 g/m(2)). The threshold shifts persisted 7 months after DFMO was discontinued. There was no obvious impact on the participant's clinical hearing, but these findings were consistent with irreversible hearing loss. This is the first case reported of irreversible ototoxicity in a clinical trial participant receiving DFMO and, thus, trial participants should be made aware of this small but important risk.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15247138

Source DB:  PubMed          Journal:  Cancer Epidemiol Biomarkers Prev        ISSN: 1055-9965            Impact factor:   4.254


  9 in total

Review 1.  Chemoprevention of hereditary colon cancers: time for new strategies.

Authors:  Luigi Ricciardiello; Dennis J Ahnen; Patrick M Lynch
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2016-04-20       Impact factor: 46.802

2.  Longitudinal assessment of air conduction audiograms in a phase III clinical trial of difluoromethylornithine and sulindac for prevention of sporadic colorectal adenomas.

Authors:  Christine E McLaren; Sharon Fujikawa-Brooks; Wen-Pin Chen; Daniel L Gillen; Daniel Pelot; Eugene W Gerner; Frank L Meyskens
Journal:  Cancer Prev Res (Phila)       Date:  2008-12

3.  Herbacetin Is a Novel Allosteric Inhibitor of Ornithine Decarboxylase with Antitumor Activity.

Authors:  Dong Joon Kim; Eunmiri Roh; Mee-Hyun Lee; Naomi Oi; Do Young Lim; Myoung Ok Kim; Young-Yeon Cho; Angelo Pugliese; Jung-Hyun Shim; Hanyong Chen; Eun Jin Cho; Jong-Eun Kim; Sun Chul Kang; Souren Paul; Hee Eun Kang; Ji Won Jung; Sung-Young Lee; Sung-Hyun Kim; Kanamata Reddy; Young Il Yeom; Ann M Bode; Zigang Dong
Journal:  Cancer Res       Date:  2015-12-16       Impact factor: 12.701

4.  Multitargeted low-dose GLAD combination chemoprevention: a novel and promising approach to combat colon carcinogenesis.

Authors:  Altaf Mohammed; Naveena B Janakiram; Misty Brewer; Krishna Vedala; Vernon E Steele; Chinthalapally V Rao
Journal:  Neoplasia       Date:  2013-05       Impact factor: 5.715

5.  Spermine synthase deficiency leads to deafness and a profound sensitivity to alpha-difluoromethylornithine.

Authors:  Xiaojing Wang; Snezana Levic; Michael Anne Gratton; Karen Jo Doyle; Ebenezer N Yamoah; Anthony E Pegg
Journal:  J Biol Chem       Date:  2008-11-10       Impact factor: 5.157

Review 6.  Cellular and Animal Model Studies on the Growth Inhibitory Effects of Polyamine Analogues on Breast Cancer.

Authors:  T J Thomas; Thresia Thomas
Journal:  Med Sci (Basel)       Date:  2018-03-13

Review 7.  Structural Basis for Allostery in PLP-dependent Enzymes.

Authors:  Jenny U Tran; Breann L Brown
Journal:  Front Mol Biosci       Date:  2022-04-25

Review 8.  Alpha-Difluoromethylornithine, an Irreversible Inhibitor of Polyamine Biosynthesis, as a Therapeutic Strategy against Hyperproliferative and Infectious Diseases.

Authors:  Nicole LoGiudice; Linh Le; Irene Abuan; Yvette Leizorek; Sigrid C Roberts
Journal:  Med Sci (Basel)       Date:  2018-02-08

9.  Thymoquinone and Difluoromethylornithine (DFMO) Synergistically Induce Apoptosis of Human Acute T Lymphoblastic Leukemia Jurkat Cells Through the Modulation of Epigenetic Pathways.

Authors:  Mahmoud Alhosin; Syed Shoeb I Razvi; Ryan A Sheikh; Jalaluddin A Khan; Mazin A Zamzami; Hani Choudhry
Journal:  Technol Cancer Res Treat       Date:  2020 Jan-Dec
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.