Loading…
Examination of the ovotoxicity of 5-fluorouracil in mice
Purpose Undesirable side effects of cancer treatments are common and include damage to the ovary, and depletion of the follicle reserve, which if severe enough, can lead to infertility and early menopause. Antimetabolite drugs, such as 5-fluorouracil (5-FU), are not considered to be detrimental to t...
Saved in:
Published in: | Journal of assisted reproduction and genetics 2018-06, Vol.35 (6), p.1053-1060 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c470t-95c594d9680a8b43a0056eabb325ced8c3a79567cbd6d4241ee21e046785f17f3 |
---|---|
cites | cdi_FETCH-LOGICAL-c470t-95c594d9680a8b43a0056eabb325ced8c3a79567cbd6d4241ee21e046785f17f3 |
container_end_page | 1060 |
container_issue | 6 |
container_start_page | 1053 |
container_title | Journal of assisted reproduction and genetics |
container_volume | 35 |
creator | Lambouras, M. Liew, S. H. Horvay, K. Abud, H. E. Stringer, J. M. Hutt, Karla J. |
description | Purpose
Undesirable side effects of cancer treatments are common and include damage to the ovary, and depletion of the follicle reserve, which if severe enough, can lead to infertility and early menopause. Antimetabolite drugs, such as 5-fluorouracil (5-FU), are not considered to be detrimental to the ovary, but the ovotoxicity of 5-FU has not been evaluated in any detail. The purpose of this study was to evaluate the effects of 5-FU on follicle number.
Methods
In this study, adult female C57Bl6 mice (
n
= 4–6 animals/group) received a single dose of saline or 5-FU (150 mg/kg) and markers of ovarian damage and follicle depletion were assessed 12 h and 7 days later.
Results
Exposure to 5-FU did not alter primordial and primary follicle numbers. Atresia of secondary and antral follicles was increased significantly 12 h after 5-FU treatment, but atresia rates returned to levels similar to that of saline treated controls at 7 days. The number of corpora lutea were reduced 7 days after exposure to 5-FU, possibly as a consequence of earlier follicular atresia.
Conclusions
These findings suggest that a single dose of 5-FU is mildly ovotoxic, but any effects on ovarian function are likely transient because the primordial follicle population is not depleted. Collectively, these data support the notion that 5-FU is unlikely to impact on the long-term fertility of women. |
doi_str_mv | 10.1007/s10815-018-1169-6 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6030007</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2019063633</sourcerecordid><originalsourceid>FETCH-LOGICAL-c470t-95c594d9680a8b43a0056eabb325ced8c3a79567cbd6d4241ee21e046785f17f3</originalsourceid><addsrcrecordid>eNp1kU9P3DAQxa2qqEuhH4BLFakXLi7j-P8FCSEoSEhc4Gw5jgNeJfFiJyv49nhZCqUSJ1ue37yZ54fQAYHfBEAeZQKKcAxEYUKExuIL2iVcUiwpha_lDlxhYEIt0PeclwCgVU2_oUWtudK1ZrtInT3aIYx2CnGsYldN976K6zjFx-DC9LR54rjr55jinKwLfRXGagjO76OdzvbZ_3g999Dt-dnN6QW-uv5zeXpyhR2TMGHNHdes1UKBVQ2jFoALb5uG1tz5VjlqpeZCuqYVLasZ8b4mvuwsFe-I7OgeOt7qruZm8K3z45Rsb1YpDDY9mWiD-VgZw725i2sjgBbDsggcvgqk-DD7PJkhZOf73o4-ztnUQHT5ImCsoL_-Q5fF9VjsvVAgqKC0UGRLuRRzTr57W4aA2eRitrmYkovZ5GJE6fn5r4u3jr9BFKDeArmUxjuf3kd_rvoMH9KXuw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2019063633</pqid></control><display><type>article</type><title>Examination of the ovotoxicity of 5-fluorouracil in mice</title><source>Springer Nature</source><source>PubMed Central</source><creator>Lambouras, M. ; Liew, S. H. ; Horvay, K. ; Abud, H. E. ; Stringer, J. M. ; Hutt, Karla J.</creator><creatorcontrib>Lambouras, M. ; Liew, S. H. ; Horvay, K. ; Abud, H. E. ; Stringer, J. M. ; Hutt, Karla J.</creatorcontrib><description>Purpose
Undesirable side effects of cancer treatments are common and include damage to the ovary, and depletion of the follicle reserve, which if severe enough, can lead to infertility and early menopause. Antimetabolite drugs, such as 5-fluorouracil (5-FU), are not considered to be detrimental to the ovary, but the ovotoxicity of 5-FU has not been evaluated in any detail. The purpose of this study was to evaluate the effects of 5-FU on follicle number.
Methods
In this study, adult female C57Bl6 mice (
n
= 4–6 animals/group) received a single dose of saline or 5-FU (150 mg/kg) and markers of ovarian damage and follicle depletion were assessed 12 h and 7 days later.
Results
Exposure to 5-FU did not alter primordial and primary follicle numbers. Atresia of secondary and antral follicles was increased significantly 12 h after 5-FU treatment, but atresia rates returned to levels similar to that of saline treated controls at 7 days. The number of corpora lutea were reduced 7 days after exposure to 5-FU, possibly as a consequence of earlier follicular atresia.
Conclusions
These findings suggest that a single dose of 5-FU is mildly ovotoxic, but any effects on ovarian function are likely transient because the primordial follicle population is not depleted. Collectively, these data support the notion that 5-FU is unlikely to impact on the long-term fertility of women.</description><identifier>ISSN: 1058-0468</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/s10815-018-1169-6</identifier><identifier>PMID: 29589294</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>5-Fluorouracil ; Animals ; Antimetabolites, Antineoplastic - toxicity ; Apoptosis ; Cancer ; Dose-Response Relationship, Drug ; Female ; Fluorouracil - toxicity ; Follicles ; Follicular Atresia - drug effects ; Gynecology ; Human Genetics ; Infertility ; Medicine ; Medicine & Public Health ; Menopause ; Mice ; Mice, Inbred C57BL ; Ovarian Follicle - drug effects ; Ovarian Follicle - pathology ; Reproductive Medicine ; Reproductive Physiology and Disease ; Reproductive status</subject><ispartof>Journal of assisted reproduction and genetics, 2018-06, Vol.35 (6), p.1053-1060</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>Journal of Assisted Reproduction and Genetics is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-95c594d9680a8b43a0056eabb325ced8c3a79567cbd6d4241ee21e046785f17f3</citedby><cites>FETCH-LOGICAL-c470t-95c594d9680a8b43a0056eabb325ced8c3a79567cbd6d4241ee21e046785f17f3</cites><orcidid>0000-0002-5111-8389</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030007/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030007/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,725,778,782,883,27911,27912,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29589294$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lambouras, M.</creatorcontrib><creatorcontrib>Liew, S. H.</creatorcontrib><creatorcontrib>Horvay, K.</creatorcontrib><creatorcontrib>Abud, H. E.</creatorcontrib><creatorcontrib>Stringer, J. M.</creatorcontrib><creatorcontrib>Hutt, Karla J.</creatorcontrib><title>Examination of the ovotoxicity of 5-fluorouracil in mice</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><addtitle>J Assist Reprod Genet</addtitle><description>Purpose
Undesirable side effects of cancer treatments are common and include damage to the ovary, and depletion of the follicle reserve, which if severe enough, can lead to infertility and early menopause. Antimetabolite drugs, such as 5-fluorouracil (5-FU), are not considered to be detrimental to the ovary, but the ovotoxicity of 5-FU has not been evaluated in any detail. The purpose of this study was to evaluate the effects of 5-FU on follicle number.
Methods
In this study, adult female C57Bl6 mice (
n
= 4–6 animals/group) received a single dose of saline or 5-FU (150 mg/kg) and markers of ovarian damage and follicle depletion were assessed 12 h and 7 days later.
Results
Exposure to 5-FU did not alter primordial and primary follicle numbers. Atresia of secondary and antral follicles was increased significantly 12 h after 5-FU treatment, but atresia rates returned to levels similar to that of saline treated controls at 7 days. The number of corpora lutea were reduced 7 days after exposure to 5-FU, possibly as a consequence of earlier follicular atresia.
Conclusions
These findings suggest that a single dose of 5-FU is mildly ovotoxic, but any effects on ovarian function are likely transient because the primordial follicle population is not depleted. Collectively, these data support the notion that 5-FU is unlikely to impact on the long-term fertility of women.</description><subject>5-Fluorouracil</subject><subject>Animals</subject><subject>Antimetabolites, Antineoplastic - toxicity</subject><subject>Apoptosis</subject><subject>Cancer</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Fluorouracil - toxicity</subject><subject>Follicles</subject><subject>Follicular Atresia - drug effects</subject><subject>Gynecology</subject><subject>Human Genetics</subject><subject>Infertility</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Menopause</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Ovarian Follicle - drug effects</subject><subject>Ovarian Follicle - pathology</subject><subject>Reproductive Medicine</subject><subject>Reproductive Physiology and Disease</subject><subject>Reproductive status</subject><issn>1058-0468</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kU9P3DAQxa2qqEuhH4BLFakXLi7j-P8FCSEoSEhc4Gw5jgNeJfFiJyv49nhZCqUSJ1ue37yZ54fQAYHfBEAeZQKKcAxEYUKExuIL2iVcUiwpha_lDlxhYEIt0PeclwCgVU2_oUWtudK1ZrtInT3aIYx2CnGsYldN976K6zjFx-DC9LR54rjr55jinKwLfRXGagjO76OdzvbZ_3g999Dt-dnN6QW-uv5zeXpyhR2TMGHNHdes1UKBVQ2jFoALb5uG1tz5VjlqpeZCuqYVLasZ8b4mvuwsFe-I7OgeOt7qruZm8K3z45Rsb1YpDDY9mWiD-VgZw725i2sjgBbDsggcvgqk-DD7PJkhZOf73o4-ztnUQHT5ImCsoL_-Q5fF9VjsvVAgqKC0UGRLuRRzTr57W4aA2eRitrmYkovZ5GJE6fn5r4u3jr9BFKDeArmUxjuf3kd_rvoMH9KXuw</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Lambouras, M.</creator><creator>Liew, S. H.</creator><creator>Horvay, K.</creator><creator>Abud, H. E.</creator><creator>Stringer, J. M.</creator><creator>Hutt, Karla J.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5111-8389</orcidid></search><sort><creationdate>20180601</creationdate><title>Examination of the ovotoxicity of 5-fluorouracil in mice</title><author>Lambouras, M. ; Liew, S. H. ; Horvay, K. ; Abud, H. E. ; Stringer, J. M. ; Hutt, Karla J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-95c594d9680a8b43a0056eabb325ced8c3a79567cbd6d4241ee21e046785f17f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>5-Fluorouracil</topic><topic>Animals</topic><topic>Antimetabolites, Antineoplastic - toxicity</topic><topic>Apoptosis</topic><topic>Cancer</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Fluorouracil - toxicity</topic><topic>Follicles</topic><topic>Follicular Atresia - drug effects</topic><topic>Gynecology</topic><topic>Human Genetics</topic><topic>Infertility</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Menopause</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Ovarian Follicle - drug effects</topic><topic>Ovarian Follicle - pathology</topic><topic>Reproductive Medicine</topic><topic>Reproductive Physiology and Disease</topic><topic>Reproductive status</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lambouras, M.</creatorcontrib><creatorcontrib>Liew, S. H.</creatorcontrib><creatorcontrib>Horvay, K.</creatorcontrib><creatorcontrib>Abud, H. E.</creatorcontrib><creatorcontrib>Stringer, J. M.</creatorcontrib><creatorcontrib>Hutt, Karla J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of assisted reproduction and genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lambouras, M.</au><au>Liew, S. H.</au><au>Horvay, K.</au><au>Abud, H. E.</au><au>Stringer, J. M.</au><au>Hutt, Karla J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Examination of the ovotoxicity of 5-fluorouracil in mice</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><stitle>J Assist Reprod Genet</stitle><addtitle>J Assist Reprod Genet</addtitle><date>2018-06-01</date><risdate>2018</risdate><volume>35</volume><issue>6</issue><spage>1053</spage><epage>1060</epage><pages>1053-1060</pages><issn>1058-0468</issn><eissn>1573-7330</eissn><abstract>Purpose
Undesirable side effects of cancer treatments are common and include damage to the ovary, and depletion of the follicle reserve, which if severe enough, can lead to infertility and early menopause. Antimetabolite drugs, such as 5-fluorouracil (5-FU), are not considered to be detrimental to the ovary, but the ovotoxicity of 5-FU has not been evaluated in any detail. The purpose of this study was to evaluate the effects of 5-FU on follicle number.
Methods
In this study, adult female C57Bl6 mice (
n
= 4–6 animals/group) received a single dose of saline or 5-FU (150 mg/kg) and markers of ovarian damage and follicle depletion were assessed 12 h and 7 days later.
Results
Exposure to 5-FU did not alter primordial and primary follicle numbers. Atresia of secondary and antral follicles was increased significantly 12 h after 5-FU treatment, but atresia rates returned to levels similar to that of saline treated controls at 7 days. The number of corpora lutea were reduced 7 days after exposure to 5-FU, possibly as a consequence of earlier follicular atresia.
Conclusions
These findings suggest that a single dose of 5-FU is mildly ovotoxic, but any effects on ovarian function are likely transient because the primordial follicle population is not depleted. Collectively, these data support the notion that 5-FU is unlikely to impact on the long-term fertility of women.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>29589294</pmid><doi>10.1007/s10815-018-1169-6</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-5111-8389</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1058-0468 |
ispartof | Journal of assisted reproduction and genetics, 2018-06, Vol.35 (6), p.1053-1060 |
issn | 1058-0468 1573-7330 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6030007 |
source | Springer Nature; PubMed Central |
subjects | 5-Fluorouracil Animals Antimetabolites, Antineoplastic - toxicity Apoptosis Cancer Dose-Response Relationship, Drug Female Fluorouracil - toxicity Follicles Follicular Atresia - drug effects Gynecology Human Genetics Infertility Medicine Medicine & Public Health Menopause Mice Mice, Inbred C57BL Ovarian Follicle - drug effects Ovarian Follicle - pathology Reproductive Medicine Reproductive Physiology and Disease Reproductive status |
title | Examination of the ovotoxicity of 5-fluorouracil in mice |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T18%3A55%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Examination%20of%20the%20ovotoxicity%20of%205-fluorouracil%20in%20mice&rft.jtitle=Journal%20of%20assisted%20reproduction%20and%20genetics&rft.au=Lambouras,%20M.&rft.date=2018-06-01&rft.volume=35&rft.issue=6&rft.spage=1053&rft.epage=1060&rft.pages=1053-1060&rft.issn=1058-0468&rft.eissn=1573-7330&rft_id=info:doi/10.1007/s10815-018-1169-6&rft_dat=%3Cproquest_pubme%3E2019063633%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c470t-95c594d9680a8b43a0056eabb325ced8c3a79567cbd6d4241ee21e046785f17f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2019063633&rft_id=info:pmid/29589294&rfr_iscdi=true |