The CSB repair factor is overexpressed in cancer cells,increases apoptotic resistance,and promotes tumor growth |
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Authors: | Manuela Caputo Mattia Frontini Renier Velez-Cruz Serena Nicolai Giorgio Prantera Luca Proietti-De-Santis |
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Affiliation: | 1. Unit of Molecular Genetics of Aging, Department of Ecology and Biology, University of Tuscia, 01100 Viterbo, Italy;2. Department of Haematology, University of Cambridge, CB2 0PT Cambridge, United Kingdom;3. The University of Texas MD Anderson Cancer Center, Department of Molecular Carcinogenesis, Science Park Division, Smithville, TX 78657, USA |
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Abstract: | In the present study we show that a number of cancer cell lines from different tissues display dramatically increased expression of the Cockayne Syndrome group B (CSB) protein, a DNA repair factor, that has recently been shown to be involved in cell robustness. Furthermore, we demonstrated that ablation of this protein by antisense technology causes devastating effects on tumor cells through a drastic reduction of cell proliferation and massive induction of apoptosis, while non-transformed cells remain unaffected. Finally, suppression of CSB in cancer cells makes these cells hypersensitive to a variety of commonly used cancer chemotherapeutic agents. Based on these results, we conclude that cancer cells overexpress CSB protein in order to enhance their anti-apoptotic capacity. The fact that CSB suppression specifically affects only cancerous cells, without harming healthy cells, suggests that CSB may be a very attractive target for the development of new anticancer therapies. |
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