Literature DB >> 21707488

Ceramidases in hematological malignancies: senseless or neglected target?

Gemma Fabrias1, Carmen Bedia, Josefina Casas, Jose Luis Abad, Antonio Delgado.   

Abstract

Ceramidases are ubiquitous amidohydrolases that catalyze the cleavage of ceramides into sphingosine and fatty acids. This reaction exerts a cytoprotective role in physiological conditions, while altered ceramidase activities favour a number of human diseases. Among these diseases, several reports point to important roles of ceramidases, mainly the acid ceramidase, in the initiation and progression of cancer, and the response of tumors to radio- or chemotherapy. Multiple reports confirm the interest of acid ceramidase inhibitors as anticancer drugs, either alone or in combination with other therapies. Sphingolipid metabolism plays a role in hematological malignancies and appears as an interesting target for therapeutic intervention. Although the use of ceramidase inhibitors in chemotherapy of hematologic cancers has not been widely investigated, a number of indirect evidence suggest that inhibition of specific ceramidases could potentiate the effect of drugs in clinical use to treat hematologic malignancies and may afford strategies to combat relapses. The arsenal of ceramidase inhibitors so far available is wide and hopefully, upcoming research will assess the feasibility of this approach.

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Year:  2011        PMID: 21707488     DOI: 10.2174/187152011797655104

Source DB:  PubMed          Journal:  Anticancer Agents Med Chem        ISSN: 1871-5206            Impact factor:   2.505


  7 in total

Review 1.  Tamoxifen regulation of sphingolipid metabolism--Therapeutic implications.

Authors:  Samy A F Morad; Myles C Cabot
Journal:  Biochim Biophys Acta       Date:  2015-05-09

2.  Dynamics of ceramide generation and metabolism in response to fenretinide--Diversity within and among leukemia.

Authors:  Samy A F Morad; Traci S Davis; Mark Kester; Thomas P Loughran; Myles C Cabot
Journal:  Leuk Res       Date:  2015-07-02       Impact factor: 3.156

3.  The antiproliferative effect of C2-ceramide on lung cancer cells through apoptosis by inhibiting Akt and NFκB.

Authors:  I-Ling Lin; Han-Lin Chou; Jin-Ching Lee; Feng-Wei Chen; Yao Fong; Wei-Chiao Chang; Hurng Wern Huang; Chang-Yi Wu; Wen-Tsan Chang; Hui-Min David Wang; Chien-Chih Chiu
Journal:  Cancer Cell Int       Date:  2014-01-06       Impact factor: 5.722

4.  C2-Ceramide-Induced Rb-Dominant Senescence-Like Phenotype Leads to Human Breast Cancer MCF-7 Escape from p53-Dependent Cell Death.

Authors:  Wen-Tsan Chang; Chang-Yi Wu; Yin-Chieh Lin; Min-Tsui Wu; Kai-Li Su; Shyng-Shiou Yuan; Hui-Min David Wang; Yao Fong; Yi-Hsiung Lin; Chien-Chih Chiu
Journal:  Int J Mol Sci       Date:  2019-09-02       Impact factor: 5.923

Review 5.  Lysosomal Ceramide Metabolism Disorders: Implications in Parkinson's Disease.

Authors:  Silvia Paciotti; Elisabetta Albi; Lucilla Parnetti; Tommaso Beccari
Journal:  J Clin Med       Date:  2020-02-21       Impact factor: 4.241

6.  Click and count: specific detection of acid ceramidase activity in live cells.

Authors:  Mireia Casasampere; Eduardo Izquierdo; Josefina Casas; José Luís Abad; Xiao Liu; Ruijuan Xu; Cungui Mao; Young-Tae Chang; Antonio Delgado; Gemma Fabrias
Journal:  Chem Sci       Date:  2020-10-22       Impact factor: 9.825

7.  Exogenous C₈-Ceramide Induces Apoptosis by Overproduction of ROS and the Switch of Superoxide Dismutases SOD1 to SOD2 in Human Lung Cancer Cells.

Authors:  Yuli C Chang; Yao Fong; Eing-Mei Tsai; Ya-Gin Chang; Han Lin Chou; Chang-Yi Wu; Yen-Ni Teng; Ta-Chih Liu; Shyng-Shiou Yuan; Chien-Chih Chiu
Journal:  Int J Mol Sci       Date:  2018-10-02       Impact factor: 5.923

  7 in total

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