Abstract
Interferon-β (IFN-β) has been widely used in cancer therapy, but the clinical trial results are generally disappointing. Our previous studies have shown that an oncolytic adenovirus carrying IFN-β (ZD55-IFN-β) exhibits significant anti-tumor activities. However, the underlying mechanisms are not clear. Here we showed that ZD55-IFN-β infection-induced S-phase cell cycle arrest in a p53-dependent manner by activating the ataxia telangiectasia mutated-dependent DNA damage pathway. In addition, ZD55-IFN-β infection could initiate both caspase-dependent apoptosis and necroptosis in cancer cells. More importantly, ZD55-IFN-β showed a synergistic effect on cancer cells when combined with doxorubicin. These results suggest that the combination of ZD55-IFN-β with doxorubicin may represent a promising clinical strategy in cancer therapy.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenoviridae / genetics
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Antibiotics, Antineoplastic / pharmacology
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Apoptosis / drug effects
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Apoptosis / physiology*
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Ataxia Telangiectasia Mutated Proteins
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Blotting, Western
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Cell Cycle Checkpoints / drug effects
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Cell Cycle Checkpoints / physiology*
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Cell Cycle Proteins / metabolism
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Cell Line, Tumor
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Cell Survival / drug effects
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Cell Survival / physiology
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DNA-Binding Proteins / metabolism
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Doxorubicin / pharmacology
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Green Fluorescent Proteins / genetics
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Green Fluorescent Proteins / metabolism
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HEK293 Cells
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Humans
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Interferon-beta / genetics
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Interferon-beta / metabolism
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Interferon-beta / physiology*
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MCF-7 Cells
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Microscopy, Confocal
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Mutation
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Necrosis
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Neoplasms / genetics
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Neoplasms / metabolism
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Neoplasms / pathology
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Oncolytic Viruses / genetics
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Protein Serine-Threonine Kinases / metabolism
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S Phase / drug effects
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S Phase / physiology*
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Tumor Suppressor Protein p53 / genetics
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Tumor Suppressor Protein p53 / metabolism
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Tumor Suppressor Proteins / metabolism
Substances
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Antibiotics, Antineoplastic
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Cell Cycle Proteins
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DNA-Binding Proteins
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Tumor Suppressor Protein p53
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Tumor Suppressor Proteins
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Green Fluorescent Proteins
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Interferon-beta
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Doxorubicin
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ATM protein, human
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Ataxia Telangiectasia Mutated Proteins
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Protein Serine-Threonine Kinases