Literature DB >> 34161570

Cyclophosphamide-Induced Inflammation of Taste Buds and Cytoprotection by Amifostine.

Anish A Sarkar1, David M Allyn1,2, Rona J Delay1, Eugene R Delay1.   

Abstract

Taste buds in the oral cavity have a complex immune system regulating normal functions and inflammatory reactions. Cyclophosphamide (CYP), a chemotherapy drug, has wide-ranging disruptive effects on the taste system including loss of taste function, taste sensory cells, and capacity for taste cell renewal. In bladder epithelium, CYP also induces inflammation. To determine if CYP induces inflammation in taste buds, we used immunohistochemistry to examine tumor necrosis factor alpha (TNF-α) (a proinflammatory cytokine) expression over a 72-hour period. Expression of TNF-α increased in a subset of PLCβ2 labeled (Type II) cells, but not SNAP-25 labeled (Type III) cells, between 8 and 24 h postinjection and declined slowly thereafter. This inflammatory response may play an important role in the disruptive effects of CYP on the taste system. Further, pretreatment with amifostine, a sulfhydryl drug known to protect normal tissues during chemo- or radiation therapy, reduced the amount of CYP-induced TNF-α expression in taste buds, suggesting this drug is capable of protecting normal cells of the taste system from adverse effects of CYP. Amifostine, used as a pretreatment to CYP and possibly other chemotherapy drugs, may offer clinical support for preventing negative side effects of chemotherapy on the taste system.
© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  TNF-α; chemotherapy; circumvallate; fungiform; immune system; taste cells

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Substances:

Year:  2021        PMID: 34161570      PMCID: PMC8345827          DOI: 10.1093/chemse/bjab031

Source DB:  PubMed          Journal:  Chem Senses        ISSN: 0379-864X            Impact factor:   4.985


  59 in total

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Review 2.  Amifostine: an update on its clinical status as a cytoprotectant in patients with cancer receiving chemotherapy or radiotherapy and its potential therapeutic application in myelodysplastic syndrome.

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Journal:  Int J Radiat Oncol Biol Phys       Date:  1984-09       Impact factor: 7.038

4.  Cytotoxicity, DNA cross-linking, and single strand breaks induced by activated cyclophosphamide and acrolein in human leukemia cells.

Authors:  T R Crook; R L Souhami; A E McLean
Journal:  Cancer Res       Date:  1986-10       Impact factor: 12.701

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Review 7.  Cyclophosphamide: review of its mutagenicity for an assessment of potential germ cell risks.

Authors:  D Anderson; J B Bishop; R C Garner; P Ostrosky-Wegman; P B Selby
Journal:  Mutat Res       Date:  1995-08       Impact factor: 2.433

8.  Correction: Pre-Treatment with Amifostine Protects against Cyclophosphamide-Induced Disruption of Taste in Mice.

Authors:  Nabanita Mukherjee; Brittany L Carroll; Jeffrey L Spees; Eugene R Delay
Journal:  PLoS One       Date:  2013-07-31       Impact factor: 3.240

9.  Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal.

Authors:  Eugene R Delay; Sarah H Socia; Jessica L Girardin; Benjamin C Jewkes; John H King; Rona J Delay
Journal:  PLoS One       Date:  2019-04-04       Impact factor: 3.240

Review 10.  Chemosensory Changes from Cancer Treatment and Their Effects on Patients' Food Behavior: A Scoping Review.

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Journal:  Nutrients       Date:  2019-09-24       Impact factor: 5.717

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2.  Impact of Co-Administration of N-Acetylcysteine and Vitamin E on Cyclophosphamide-Induced Ovarian Toxicity in Female Rats.

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