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Preclinical characterization of AEG35156/GEM 640, a second-generation antisense oligonucleotide targeting X-linked inhibitor of apoptosis.

Preclinical characterization of AEG35156/GEM 640, a second-generation antisense oligonucleotide targeting X-linked inhibitor of apoptosis. Research Abstract Details 

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  • Preclinical characterization of AEG35156/GEM 640, a second-generation antisense oligonucleotide targeting X-linked inhibitor of apoptosis. Abstract Text:

    eric c lacasseEric C LaCasse,gabriele g cherton-horvatGabriele G Cherton-Horvat,kimberley e hewittKimberley E Hewitt,lori j jeromeLori J Jerome,stephen j morrisStephen J Morris,ekambar r kandimallaEkambar R Kandimalla,dong yuDong Yu,hui wangHui Wang,wei wangWei Wang,ruiwen zhangRuiwen Zhang,sudhir agrawalSudhir Agrawal,john w gillardJohn W Gillard,jon p durkinJon P Durkin,

    PURPOSE: Cancer cells can use X-linked inhibitor of apoptosis (XIAP) to evade apoptotic cues, including chemotherapy. The antitumor potential of AEG35156, a novel second-generation antisense oligonucleotide directed toward XIAP, was assessed in human cancer models when given as a single agent and in combination with clinically relevant chemotherapeutics. EXPERIMENTAL DESIGN: AEG35156 was characterized for its ability to cause dose-dependent reductions of XIAP mRNA and protein in vitro and in vivo, to sensitize cancer cell lines to death stimuli, and to exhibit antitumor activity in multiple human cancer xenograft models as a single agent or in combination with chemotherapy. RESULTS: AEG35156 reduced XIAP mRNA levels with an EC50 of 8 to 32 nmol/L and decreased XIAP protein levels by >80%. Loss of XIAP protein correlated with increased sensitization to tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-mediated apoptosis in Panc-1 pancreatic carcinoma cells. AEG35156 exhibited potent antitumor activity relative to control oligonucleotides in three human cancer xenograft models (prostate, colon, and lung) and was capable of inducing complete tumor regression when combined with taxanes. Antitumor effects of AEG35156 correlated with suppression of tumor XIAP levels. CONCLUSIONS: AEG35156 reduces XIAP levels and sensitizes tumors to chemotherapy. AEG35156 is presently under clinical assessment in multiple phase I trials in cancer patients as a single agent and in combination with docetaxel in solid tumors or cytarabine/idarubicin in leukemia.

    Preclinical characterization of AEG35156/GEM 640, a second-generation antisense oligonucleotide targeting X-linked inhibitor of apoptosis. Publishing Authors By Initials

    ec lacasseEC LaCasse,gg cherton-horvatGG Cherton-Horvat,ke hewittKE Hewitt,lj jeromeLJ Jerome,sj morrisSJ Morris,er kandimallaER Kandimalla,d yuD Yu,h wangH Wang,w wangW Wang,r zhangR Zhang,s agrawalS Agrawal,jw gillardJW Gillard,jp durkinJP Durkin,

    For similar abstracts research abstracts see: abstracts research

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    Preclinical characterization of AEG35156/GEM 640, a second-generation antisense oligonucleotide targeting X-linked inhibitor of apoptosis. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Clinical cancer research : an official journal of

    VOLUME: 12

    Page Numbers: 5231-41

    Journal Abbreviation:

    ISSN: 1078-0432

    DAY: 1

    MONTH: Sep

    YEAR: 2006

    Preclinical characterization of AEG35156/GEM 640, a second-generation antisense oligonucleotide targeting X-linked inhibitor of apoptosis. Information

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    LANGUAGE: eng

    NlmUniqueID: 9502500

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    Grant and Affiliation Information for Preclinical characterization of AEG35156/GEM 640, a second-generation antisense oligonucleotide targeting X-linked inhibitor of apoptosis.

    AFFILIATION: Aegera Therapeutics, Inc., Montreal, Quebec, Canada.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Clin Cancer Res

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