ZHAO Ling-zho, ZHANG Hua-bei. Research Progress of PARP-1 Inhibitors in Antitumor Drugs and Radionuclide Markers[J]. Journal of Isotopes, 2011, 24(增刊): 45-58. DOI: 10.7538/tws.2011.24.增刊.0045
Citation: ZHAO Ling-zho, ZHANG Hua-bei. Research Progress of PARP-1 Inhibitors in Antitumor Drugs and Radionuclide Markers[J]. Journal of Isotopes, 2011, 24(增刊): 45-58. DOI: 10.7538/tws.2011.24.增刊.0045

Research Progress of PARP-1 Inhibitors in Antitumor Drugs and Radionuclide Markers

  • Poly(ADPribose)polymerase (PARP) is a new target in the cancer treatment nowadays. PARP not only can repair DNA damage, regulate and control transcription, maintain the stability of intracellular environment and genome, regulate the process of cell survival and death, but also is the main transcription factor in the development of inflammation and the process of cancer. To inhibit PARP activity can reduce the DNA repair function in tumor cells, and increase the sensibility to DNA damage agents, so as to improve the efficacy of radiation therapy and chemotherapy for tumor. A number of studies have suggested that, whether used alone or combination with other chemotherapy drugs, PARP inhibitors show the potential in the anti-tumor therapeutic areas. In this paper, PARP-1 inhibitors were reviewed in antitumor research progress. According to the stage of development, PARP-1 inhibitors are classified. Several representative PARP-1 inhibitors, in clinical trials, with potential clinical value were introduced. Positron emission tomography (PET), uses the main short half-life elementary in human body as tracer, and at the molecular level, achieve the no wound, quantitative and dynamic observation about the different changes of metabolites or drugs in the body. PET is the most advanced contemporary video diagnostic technology, and this paper simply introduce the research progress of PARP-1 inhibitors labeled with radioactive nuclides.
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