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First inhibitor for enzyme linked to cancers created

Date:
November 20, 2014
Source:
University of California - Irvine
Summary:
Recent studies showing acid ceramidase (AC) to be upregulated in melanoma, lung and prostate cancers have made the enzyme a desired target for novel synthetic inhibitor compounds. Now scientists describe the very first class of AC inhibitors that may aid in the efficacy of chemotherapies.
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Recent studies showing acid ceramidase (AC) to be upregulated in melanoma, lung and prostate cancers have made the enzyme a desired target for novel synthetic inhibitor compounds. This week in Angewandte Chemie, scientists with UC Irvine School of Medicine and the Italian Institute of Technology describe the very first class of AC inhibitors that may aid in the efficacy of chemotherapies.

AC, which is encoded by the ASAH1 gene, plays an important role in the regulation of cell fate, setting the balance between pro-aging/death and pro-life signals. Mutations in the ASAH1 gene have been associated with a lysosomal storage disorder called Farber disease and with spinal muscular atrophy.

In their Angewandte Chemie study, UC Irvine's Daniele Piomelli -- the Louise Turner Arnold Chair in the Neurosciences -- and colleagues present a potent and systematically active small-molecule inhibitor of intracellular AC.

In in vivo studies, the team found that inhibiting AC with their novel compound tilts the balance between pro-aging/death and pro-life chemical signals, favoring the former at the expense of the latter.

"We hope that AC inhibitors may be one day used as 'chemosensitizers' -- drugs that enhance the cancer-killing power of anti-tumoral drugs," said Piomelli, a professor in the Department of Anatomy & Neurobiology who also is affiliated with UC Irvine Chao Family Comprehensive Cancer Center.

"The new chemical scaffold we published is a promising starting point for the development of novel therapeutic agents, and we aim to pursue its further pharmaceutical development."


Story Source:

Materials provided by University of California - Irvine. Note: Content may be edited for style and length.


Journal Reference:

  1. Daniela Pizzirani, Anders Bach, Natalia Realini, Andrea Armirotti, Luisa Mengatto, Inga Bauer, Stefania Girotto, Chiara Pagliuca, Marco De Vivo, Maria Summa, Alison Ribeiro, Daniele Piomelli. Benzoxazolone Carboxamides: Potent and Systemically Active Inhibitors of Intracellular Acid Ceramidase. Angewandte Chemie International Edition, 2014; DOI: 10.1002/anie.201409042

Cite This Page:

University of California - Irvine. "First inhibitor for enzyme linked to cancers created." ScienceDaily. ScienceDaily, 20 November 2014. <www.sciencedaily.com/releases/2014/11/141120183627.htm>.
University of California - Irvine. (2014, November 20). First inhibitor for enzyme linked to cancers created. ScienceDaily. Retrieved October 30, 2024 from www.sciencedaily.com/releases/2014/11/141120183627.htm
University of California - Irvine. "First inhibitor for enzyme linked to cancers created." ScienceDaily. www.sciencedaily.com/releases/2014/11/141120183627.htm (accessed October 30, 2024).

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