Repurposing Drugs in Oncology (ReDO)—clarithromycin as an anti-cancer agent

Clarithromycin (CAM) is a well-known macrolide antibiotic available as a generic drug. CAM is traditionally used for many types of bacterial infections, treatment of Lyme disease and eradication of gastric infection with Helicobacter pylori. Extensive preclinical and clinical data demonstrate a pote...

Full description

Saved in:
Bibliographic Details
Published inEcancermedicalscience Vol. 9; p. 513
Main Author Van Nuffel, An MT
Format Journal Article
LanguageEnglish
Published England Cancer Intelligence 24.02.2015
Subjects
Online AccessGet full text
ISSN1754-6605
1754-6605
DOI10.3332/ecancer.2015.513

Cover

Abstract Clarithromycin (CAM) is a well-known macrolide antibiotic available as a generic drug. CAM is traditionally used for many types of bacterial infections, treatment of Lyme disease and eradication of gastric infection with Helicobacter pylori. Extensive preclinical and clinical data demonstrate a potential role for CAM to treat various tumours in combination with conventional treatment. The mechanisms of action underlying the anti-tumour activity of CAM are multiple and include prolonged reduction of pro-inflammatory cytokines, autophagy inhibition, and anti-angiogenesis. Here, we present an overview of the current preclinical (in vitro and in vivo) and clinical evidence supporting the role of CAM in cancer. Overall these findings justify further research with CAM in many tumour types, with multiple myeloma, lymphoma, chronic myeloid leukaemia (CML), and lung cancer having the highest level of evidence. Finally, a series of proposals are being made to further investigate the use of CAM in clinical trials which offer the greatest prospect of clinical benefit to patients.
AbstractList Clarithromycin (CAM) is a well-known macrolide antibiotic available as a generic drug. CAM is traditionally used for many types of bacterial infections, treatment of Lyme disease and eradication of gastric infection with Helicobacter pylori. Extensive preclinical and clinical data demonstrate a potential role for CAM to treat various tumours in combination with conventional treatment. The mechanisms of action underlying the anti-tumour activity of CAM are multiple and include prolonged reduction of pro-inflammatory cytokines, autophagy inhibition, and anti-angiogenesis. Here, we present an overview of the current preclinical (in vitro and in vivo) and clinical evidence supporting the role of CAM in cancer. Overall these findings justify further research with CAM in many tumour types, with multiple myeloma, lymphoma, chronic myeloid leukaemia (CML), and lung cancer having the highest level of evidence. Finally, a series of proposals are being made to further investigate the use of CAM in clinical trials which offer the greatest prospect of clinical benefit to patients.
Clarithromycin (CAM) is a well-known macrolide antibiotic available as a generic drug. CAM is traditionally used for many types of bacterial infections, treatment of Lyme disease and eradication of gastric infection with Helicobacter pylori . Extensive preclinical and clinical data demonstrate a potential role for CAM to treat various tumours in combination with conventional treatment. The mechanisms of action underlying the anti-tumour activity of CAM are multiple and include prolonged reduction of pro-inflammatory cytokines, autophagy inhibition, and anti-angiogenesis. Here, we present an overview of the current preclinical ( in vitro and in vivo ) and clinical evidence supporting the role of CAM in cancer. Overall these findings justify further research with CAM in many tumour types, with multiple myeloma, lymphoma, chronic myeloid leukaemia (CML), and lung cancer having the highest level of evidence. Finally, a series of proposals are being made to further investigate the use of CAM in clinical trials which offer the greatest prospect of clinical benefit to patients.
Clarithromycin (CAM) is a well-known macrolide antibiotic available as a generic drug. CAM is traditionally used for many types of bacterial infections, treatment of Lyme disease and eradication of gastric infection with Helicobacter pylori. Extensive preclinical and clinical data demonstrate a potential role for CAM to treat various tumours in combination with conventional treatment. The mechanisms of action underlying the anti-tumour activity of CAM are multiple and include prolonged reduction of pro-inflammatory cytokines, autophagy inhibition, and anti-angiogenesis. Here, we present an overview of the current preclinical (in vitro and in vivo) and clinical evidence supporting the role of CAM in cancer. Overall these findings justify further research with CAM in many tumour types, with multiple myeloma, lymphoma, chronic myeloid leukaemia (CML), and lung cancer having the highest level of evidence. Finally, a series of proposals are being made to further investigate the use of CAM in clinical trials which offer the greatest prospect of clinical benefit to patients.Clarithromycin (CAM) is a well-known macrolide antibiotic available as a generic drug. CAM is traditionally used for many types of bacterial infections, treatment of Lyme disease and eradication of gastric infection with Helicobacter pylori. Extensive preclinical and clinical data demonstrate a potential role for CAM to treat various tumours in combination with conventional treatment. The mechanisms of action underlying the anti-tumour activity of CAM are multiple and include prolonged reduction of pro-inflammatory cytokines, autophagy inhibition, and anti-angiogenesis. Here, we present an overview of the current preclinical (in vitro and in vivo) and clinical evidence supporting the role of CAM in cancer. Overall these findings justify further research with CAM in many tumour types, with multiple myeloma, lymphoma, chronic myeloid leukaemia (CML), and lung cancer having the highest level of evidence. Finally, a series of proposals are being made to further investigate the use of CAM in clinical trials which offer the greatest prospect of clinical benefit to patients.
Author Van Nuffel, An MT
Author_xml – sequence: 1
  givenname: An MT
  surname: Van Nuffel
  fullname: Van Nuffel, An MT
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25729426$$D View this record in MEDLINE/PubMed
BookMark eNp1kUtLxDAUhYMovveupEtddMy77UYQ36AMiPuQZm5rpJOMSSvMzh_hL_SXmGFGUcFNEsh3zrncs4PWnXeA0AHBI8YYPQGjnYEwopiIkSBsDW2TQvBcSizWf7y30E6MzxhLUlGxibaoKGjFqdxG9w8wG8LMR-va7CIMbcysy8bO-M638-zoAS7Gxx9v76bTwfZPwU_nJgE6Zjqdrrf5coRMt-D6PbTR6C7C_ureRY9Xl4_nN_nd-Pr2_OwuN1zSPq8biQtSsrokdQkYKmMqwnRNJqUAWRYTLkWDm6YBURAARvmEGSko4RVUvGS76HRpOxvqKUxMSg66U7NgpzrMlddW_f5x9km1_lVxxklVyWRwtDII_mWA2KupjQa6TjvwQ1QkLY1zVnKR0MOfWd8hXytMAF4CJvgYAzTfCMFq0ZJataQWLanUUpLIPxJje91bv5jWdv8LPwH3x5p_
CitedBy_id crossref_primary_10_1007_s11030_024_10995_6
crossref_primary_10_1080_23723556_2020_1745038
crossref_primary_10_1111_bjh_14878
crossref_primary_10_1186_s13256_017_1550_6
crossref_primary_10_1186_s13256_018_1636_9
crossref_primary_10_1038_bcj_2016_32
crossref_primary_10_3389_fphar_2021_599598
crossref_primary_10_1016_j_oraloncology_2018_07_016
crossref_primary_10_12793_tcp_2017_25_3_134
crossref_primary_10_1371_journal_pone_0164529
crossref_primary_10_1016_j_lungcan_2016_12_010
crossref_primary_10_4251_wjgo_v14_i1_153
crossref_primary_10_1007_s15010_020_01536_y
crossref_primary_10_1016_j_leukres_2021_106523
crossref_primary_10_2174_0929867327999200817102154
crossref_primary_10_1089_jop_2018_0103
crossref_primary_10_3748_wjg_v27_i37_6290
crossref_primary_10_1016_j_bbcan_2019_188319
crossref_primary_10_1016_j_semcancer_2019_10_019
crossref_primary_10_1016_j_intimp_2016_01_021
crossref_primary_10_1021_acs_jmedchem_2c01408
crossref_primary_10_1016_j_addr_2018_08_012
crossref_primary_10_1186_s40164_018_0110_0
crossref_primary_10_1002_hon_2754
crossref_primary_10_1016_j_pupt_2021_102095
crossref_primary_10_20517_cdr_2023_108
crossref_primary_10_1080_15548627_2016_1252890
crossref_primary_10_1002_hon_2738
crossref_primary_10_1080_23808993_2017_1338920
crossref_primary_10_3389_fmicb_2022_960693
crossref_primary_10_1111_epi_13994
crossref_primary_10_1007_s00277_015_2412_1
crossref_primary_10_2174_1568026619666190119152706
crossref_primary_10_1021_acsomega_4c00617
crossref_primary_10_1186_s13046_022_02350_0
crossref_primary_10_1007_s00284_022_03089_9
crossref_primary_10_1016_j_ejps_2020_105401
crossref_primary_10_1074_jbc_RA119_010770
crossref_primary_10_1186_s40880_018_0309_9
crossref_primary_10_2147_BCTT_S270799
crossref_primary_10_1126_scitranslmed_abd5524
crossref_primary_10_3389_fphar_2018_01357
crossref_primary_10_1038_s41419_020_2349_8
ContentType Journal Article
Copyright the authors; licensee ecancermedicalscience. 2015
Copyright_xml – notice: the authors; licensee ecancermedicalscience. 2015
DBID AAYXX
CITATION
NPM
7X8
5PM
DOI 10.3332/ecancer.2015.513
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList PubMed

MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1754-6605
ExternalDocumentID PMC4341996
25729426
10_3332_ecancer_2015_513
Genre Journal Article
GroupedDBID ---
29G
2WC
53G
5GY
5VS
7X7
8FI
8FJ
AAYXX
ABDBF
ABUWG
ACUHS
ADBBV
ADRAZ
AEGXH
AFKRA
AHMBA
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BCNDV
BENPR
BPHCQ
BVXVI
CCPQU
CITATION
CS3
DIK
EBD
EBS
EJD
ESX
FRP
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
KQ8
M48
M~E
OK1
OVT
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
RNS
RPM
TR2
TUS
UKHRP
C1A
NPM
7X8
PUEGO
5PM
ID FETCH-LOGICAL-c462t-bf607183b81b8e0e9cc913ab1d85e687d465f0fffe571ee324d3c652149e9483
IEDL.DBID M48
ISSN 1754-6605
IngestDate Thu Aug 21 18:07:09 EDT 2025
Fri Sep 05 05:38:27 EDT 2025
Mon Jul 21 05:47:54 EDT 2025
Tue Jul 01 02:44:20 EDT 2025
Thu Apr 24 23:03:07 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords ReDO project
antineoplastic agents
clarithromycin
anti-bacterial agents
drug repositioning
neoplasms
Language English
License This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c462t-bf607183b81b8e0e9cc913ab1d85e687d465f0fffe571ee324d3c652149e9483
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.3332/ecancer.2015.513
PMID 25729426
PQID 1660443845
PQPubID 23479
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_4341996
proquest_miscellaneous_1660443845
pubmed_primary_25729426
crossref_primary_10_3332_ecancer_2015_513
crossref_citationtrail_10_3332_ecancer_2015_513
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2015-02-24
PublicationDateYYYYMMDD 2015-02-24
PublicationDate_xml – month: 02
  year: 2015
  text: 2015-02-24
  day: 24
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Ecancermedicalscience
PublicationTitleAlternate Ecancermedicalscience
PublicationYear 2015
Publisher Cancer Intelligence
Publisher_xml – name: Cancer Intelligence
SSID ssj0061925
Score 2.2477708
Snippet Clarithromycin (CAM) is a well-known macrolide antibiotic available as a generic drug. CAM is traditionally used for many types of bacterial infections,...
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 513
SubjectTerms Conference Report
Title Repurposing Drugs in Oncology (ReDO)—clarithromycin as an anti-cancer agent
URI https://www.ncbi.nlm.nih.gov/pubmed/25729426
https://www.proquest.com/docview/1660443845
https://pubmed.ncbi.nlm.nih.gov/PMC4341996
Volume 9
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3JatxAEC1iG4wvIZudyTJ0wIf40LY16vUQQhLbGMPYwdgwN6FulZwBR5PMAplbPiJfmC9JlSRPMokx5CIEvdC8aqleqVWvALZL5VITMUiP1kqV2CAdeRVpEx_zXoLO5Zzg3D81x5fqZKAHv9OjWwAnt4Z2XE_qcny9--3r_C098G844kzT3h5GBojFPRO9q7mE7Rr5JcOhWF8tzhQ4UtB1eqRW0hCLbw4tb51h2Un9wzz__oHyD4909ADut1RSvGts_xDuYfUI1vvtYflj6BO5JhhH_DVAHIxnVxMxrMRZVetUz8Xrczw42_n5_UckBIZcLuHznAaKfCJyulbToWzWK3JOv3oCF0eHFx-OZVs9QUZlelMZSpaOc2kgYupwH32MPknzkBROo3G2UEaX-2VZorYJIhGrIo2GvLny6MmCm7BajSp8CsIbi4EboylVEVJPrDLEwpjchRDRdGDvBq0stsriXODiOqMIg_HNWnwzxjcjfDuwsxjxpVHVuKPvqxsDZLT1-Twjr3A0m2QJWVGp1Cndga3GIIvZ6E3U88Q-OmCXTLXowLLayy3V8FMtr61Y4s6bZ_-xxuewwbd1qrt6AavT8QxfElmZhi6s2IHtwtr7w9OP59065O_W-_IXKf7uZA
linkProvider Scholars Portal
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Repurposing+Drugs+in+Oncology+%28ReDO%29%E2%80%94clarithromycin+as+an+anti-cancer+agent&rft.jtitle=Ecancermedicalscience&rft.au=Van+Nuffel%2C+An+MT&rft.date=2015-02-24&rft.issn=1754-6605&rft.eissn=1754-6605&rft.volume=9&rft_id=info:doi/10.3332%2Fecancer.2015.513&rft.externalDBID=n%2Fa&rft.externalDocID=10_3332_ecancer_2015_513
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1754-6605&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1754-6605&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1754-6605&client=summon