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Platinum-induced neurotoxicity: A review of possible mechanisms

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Ertaş, Hülya
Caner, Burcu

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Baishideng Publishing Group Inc

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Patients treated with platinum-based chemotherapy frequently experience neurotoxic symptoms, which may lead to premature discontinuation of therapy. Despite discontinuation of platinum drugs, these symptoms can persist over a long period of time. Cisplatin and oxaliplatin, among all platinum drugs, have significant neurotoxic potential. A distal dose-dependent symmetrical sensory neuropathy is the most common presentation of platinum neurotoxicity. DNA damage-induced apoptosis of dorsal root ganglion (DRG) neurons seems to be the principal cause of neurological symptoms. However, DRG injury alone cannot explain some unique symptoms such as cold-aggravated burning pain affecting distal extremities that is observed with oxaliplatin administration. In this article, we briefly reviewed potential mechanisms for the development of platinum drugs-associated neurological manifestations.

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Root ganglion neurons, Oxaliplatin-induced neurotoxicity, Induced peripheral neurotoxicity, Nerve hyperexcitability, Anticancer drug, Up-regulation, In-vitro, Cisplatin, Neuropathy, Dna, Cisplatin, Dorsal root ganglion, Mechanism, Oxaliplatin, Neurotoxicity, Neuropathic pain, Sodium channel, Science & technology, Life sciences & biomedicine, Oncology

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