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PARP inhibitors and cancer therapy - early results and potential applications.

AbstractPolyadenosine diphosphate-ribose polymerase (PARP) inhibitors are emerging as an exciting new class of agents for treating cancer. There is pre-clinical evidence for their use to potentiate both chemotherapeutic agents and radiotherapy, and also as single agents. This paper discusses the early clinical work published showing their use in combination with temozolomide in malignant melanoma, and in familial (BRCA-related) cancers.
AuthorsC Jones, E R Plummer (Affiliation: Northern Institute for Cancer Research, Newcastle University, Paul O'Gorman Building, Framlington Place, Newcastle upon Tyne NE2 4HH, UK.)
JournalThe British journal of radiology (Br J Radiol) Vol. 81 Spec No 1 Pg. S2-5 (Oct 2008) ISSN: 1748-880X [Electronic] England
PMID18819994 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Antineoplastic Agents, Alkylating
  • Enzyme Inhibitors
  • Dacarbazine
  • temozolomide
  • Poly(ADP-ribose) Polymerases
Topics
  • Animals
  • Antineoplastic Agents (therapeutic use)
  • Antineoplastic Agents, Alkylating (therapeutic use)
  • Breast Neoplasms (drug therapy, genetics)
  • Dacarbazine (analogs & derivatives, therapeutic use)
  • Enzyme Inhibitors (therapeutic use)
  • Female
  • Humans
  • Melanoma (drug therapy)
  • Mice
  • Ovarian Neoplasms (drug therapy, genetics)
  • Poly(ADP-ribose) Polymerases (antagonists & inhibitors)

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