Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse model.

<h4>Background</h4>Treatment of head and neck cancer with radiation often results in damage to surrounding normal tissues such as salivary glands. Permanent loss of function in the salivary glands often leads patients to discontinue treatment due to incapacitating side effects. It has pr...

Full description

Bibliographic Details
Main Authors: Katie L Martin, Grace A Hill, Rob R Klein, Deborah G Arnett, Randy Burd, Kirsten H Limesand
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23236487/pdf/?tool=EBI
_version_ 1818573215929204736
author Katie L Martin
Grace A Hill
Rob R Klein
Deborah G Arnett
Randy Burd
Kirsten H Limesand
author_facet Katie L Martin
Grace A Hill
Rob R Klein
Deborah G Arnett
Randy Burd
Kirsten H Limesand
author_sort Katie L Martin
collection DOAJ
description <h4>Background</h4>Treatment of head and neck cancer with radiation often results in damage to surrounding normal tissues such as salivary glands. Permanent loss of function in the salivary glands often leads patients to discontinue treatment due to incapacitating side effects. It has previously been shown that IGF-1 suppresses radiation-induced apoptosis and enhances G2/M arrest leading to preservation of salivary gland function. In an effort to recapitulate the effects of IGF-1, as well as increase the likelihood of translating these findings to the clinic, the small molecule therapeutic Roscovitine, is being tested. Roscovitine is a cyclin-dependent kinase inhibitor that acts to transiently inhibit cell cycle progression and allow for DNA repair in damaged tissues.<h4>Methodology/principal findings</h4>Treatment with Roscovitine prior to irradiation induced a significant increase in the percentage of cells in the G(2)/M phase, as demonstrated by flow cytometry. In contrast, mice treated with radiation exhibit no differences in the percentage of cells in G(2)/M when compared to unirradiated controls. Similar to previous studies utilizing IGF-1, pretreatment with Roscovitine leads to a significant up-regulation of p21 expression and a significant decrease in the number of PCNA positive cells. Radiation treatment leads to a significant increase in activated caspase-3 positive salivary acinar cells, which is suppressed by pretreatment with Roscovitine. Administration of Roscovitine prior to targeted head and neck irradiation preserves normal tissue function in mouse parotid salivary glands, both acutely and chronically, as measured by salivary output.<h4>Conclusions/significance</h4>These studies suggest that induction of transient G(2)/M cell cycle arrest by Roscovitine allows for suppression of apoptosis, thus preserving normal salivary function following targeted head and neck irradiation. This could have an important clinical impact by preventing the negative side effects of radiation therapy in surrounding normal tissues.
first_indexed 2024-12-15T00:08:13Z
format Article
id doaj.art-43e615c81dfa4af9a15f2c9251404a6e
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-15T00:08:13Z
publishDate 2012-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-43e615c81dfa4af9a15f2c9251404a6e2022-12-21T22:42:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5136310.1371/journal.pone.0051363Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse model.Katie L MartinGrace A HillRob R KleinDeborah G ArnettRandy BurdKirsten H Limesand<h4>Background</h4>Treatment of head and neck cancer with radiation often results in damage to surrounding normal tissues such as salivary glands. Permanent loss of function in the salivary glands often leads patients to discontinue treatment due to incapacitating side effects. It has previously been shown that IGF-1 suppresses radiation-induced apoptosis and enhances G2/M arrest leading to preservation of salivary gland function. In an effort to recapitulate the effects of IGF-1, as well as increase the likelihood of translating these findings to the clinic, the small molecule therapeutic Roscovitine, is being tested. Roscovitine is a cyclin-dependent kinase inhibitor that acts to transiently inhibit cell cycle progression and allow for DNA repair in damaged tissues.<h4>Methodology/principal findings</h4>Treatment with Roscovitine prior to irradiation induced a significant increase in the percentage of cells in the G(2)/M phase, as demonstrated by flow cytometry. In contrast, mice treated with radiation exhibit no differences in the percentage of cells in G(2)/M when compared to unirradiated controls. Similar to previous studies utilizing IGF-1, pretreatment with Roscovitine leads to a significant up-regulation of p21 expression and a significant decrease in the number of PCNA positive cells. Radiation treatment leads to a significant increase in activated caspase-3 positive salivary acinar cells, which is suppressed by pretreatment with Roscovitine. Administration of Roscovitine prior to targeted head and neck irradiation preserves normal tissue function in mouse parotid salivary glands, both acutely and chronically, as measured by salivary output.<h4>Conclusions/significance</h4>These studies suggest that induction of transient G(2)/M cell cycle arrest by Roscovitine allows for suppression of apoptosis, thus preserving normal salivary function following targeted head and neck irradiation. This could have an important clinical impact by preventing the negative side effects of radiation therapy in surrounding normal tissues.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23236487/pdf/?tool=EBI
spellingShingle Katie L Martin
Grace A Hill
Rob R Klein
Deborah G Arnett
Randy Burd
Kirsten H Limesand
Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse model.
PLoS ONE
title Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse model.
title_full Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse model.
title_fullStr Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse model.
title_full_unstemmed Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse model.
title_short Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse model.
title_sort prevention of radiation induced salivary gland dysfunction utilizing a cdk inhibitor in a mouse model
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23236487/pdf/?tool=EBI
work_keys_str_mv AT katielmartin preventionofradiationinducedsalivaryglanddysfunctionutilizingacdkinhibitorinamousemodel
AT graceahill preventionofradiationinducedsalivaryglanddysfunctionutilizingacdkinhibitorinamousemodel
AT robrklein preventionofradiationinducedsalivaryglanddysfunctionutilizingacdkinhibitorinamousemodel
AT deborahgarnett preventionofradiationinducedsalivaryglanddysfunctionutilizingacdkinhibitorinamousemodel
AT randyburd preventionofradiationinducedsalivaryglanddysfunctionutilizingacdkinhibitorinamousemodel
AT kirstenhlimesand preventionofradiationinducedsalivaryglanddysfunctionutilizingacdkinhibitorinamousemodel