Literature DB >> 16394139

Application of XIAP antisense to cancer and other proliferative disorders: development of AEG35156/ GEM640.

Eric C Lacasse1, Ekambar R Kandimalla, Peter Winocour, Tim Sullivan, Sudhir Agrawal, John W Gillard, Jon Durkin.   

Abstract

Targeting apoptosis control provides a novel therapeutic approach to the treatment of cancer and other proliferative disorders. We summarize the evidence for apoptosis deregulation in cancer and describe the pivotal role of XIAP, the X-linked Inhibitor-of-APoptosis. XIAP is the predominant inhibitor of caspases 3, 7 and 9 in cells, which suppresses the programmed cell death effector capability of these proteases. Evidence is presented validating XIAP as a cancer target. The inhibition or downregulation of XIAP in cancer cells lowers the apoptotic threshold, thereby inducing cell death and/or enhancing the cytotoxic action of chemotherapeutic agents. We describe the development of AEG35156 (also named GEM640), a second generation antisense compound targeting XIAP, from concept to in vivo preclinical proof-of-principle studies, through formal toxicology, and to a phase 1 clinical trial in cancer patients.

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Year:  2005        PMID: 16394139     DOI: 10.1196/annals.1359.032

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  18 in total

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3.  Regulation of colorectal cancer cell apoptosis by the n-3 polyunsaturated fatty acids Docosahexaenoic and Eicosapentaenoic.

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Review 6.  Exploiting cellular pathways to develop new treatment strategies for AML.

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7.  X-linked inhibitor of apoptosis protein and its E3 ligase activity promote transforming growth factor-{beta}-mediated nuclear factor-{kappa}B activation during breast cancer progression.

Authors:  Jason R Neil; Maozhen Tian; William P Schiemann
Journal:  J Biol Chem       Date:  2009-06-15       Impact factor: 5.157

8.  Phase I/II trial of AEG35156 X-linked inhibitor of apoptosis protein antisense oligonucleotide combined with idarubicin and cytarabine in patients with relapsed or primary refractory acute myeloid leukemia.

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Review 9.  The evolving landscape in the therapy of acute myeloid leukemia.

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Review 10.  New agents in acute myeloid leukemia: beyond cytarabine and anthracyclines.

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