Emerging Bcl-2 inhibitors for the treatment of cancer

Bcl-2 family proteins are a component of the antiapoptotic machinery and are overexpressed in different malignancies. Accordingly, their enhanced expression has been attributed to the observed chemoresistance in most of the cancers. Therefore, targeting Bcl-2 family members becomes an important and...

Full description

Saved in:
Bibliographic Details
Published inExpert opinion on emerging drugs Vol. 16; no. 1; p. 59
Main Authors Azmi, Asfar S, Wang, Zhiwei, Philip, Philip A, Mohammad, Ramzi M, Sarkar, Fazlul H
Format Journal Article
LanguageEnglish
Published England 01.03.2011
Subjects
Online AccessGet more information
ISSN1744-7623
DOI10.1517/14728214.2010.515210

Cover

Loading…
Abstract Bcl-2 family proteins are a component of the antiapoptotic machinery and are overexpressed in different malignancies. Accordingly, their enhanced expression has been attributed to the observed chemoresistance in most of the cancers. Therefore, targeting Bcl-2 family members becomes an important and attractive approach towards cancer therapy and is currently a very rapidly evolving area of research. This article highlights the numerous advancements that have been made in the design and synthesis of small molecule inhibitors (SMI) of pro-survival Bcl-2 proteins. This review comprehensively describes the progress made over the last 2 decades on this subject, including the clinical status of SMIs of Bcl-2 family proteins. Newer insights on the status of our knowledge on SMIs of Bcl-2 family proteins, their most beneficial application as well as current and future directions in this field are discussed. Targeting Bcl-2 family proteins using SMI strategies is gaining momentum, with the emergence of certain new classes of inhibitors in Phase I and II clinical settings. In view of the tremendous progress toward the development of such inhibitors, this innovative approach certainly holds promise and has the potential to become a future mainstay for cancer therapy. The stage is set for the next generation of SMIs, for not only Bcl-2 proteins but also for Mcl-1. Other emerging molecules in the apoptotic machinery will also be explored and targeted.
AbstractList Bcl-2 family proteins are a component of the antiapoptotic machinery and are overexpressed in different malignancies. Accordingly, their enhanced expression has been attributed to the observed chemoresistance in most of the cancers. Therefore, targeting Bcl-2 family members becomes an important and attractive approach towards cancer therapy and is currently a very rapidly evolving area of research. This article highlights the numerous advancements that have been made in the design and synthesis of small molecule inhibitors (SMI) of pro-survival Bcl-2 proteins. This review comprehensively describes the progress made over the last 2 decades on this subject, including the clinical status of SMIs of Bcl-2 family proteins. Newer insights on the status of our knowledge on SMIs of Bcl-2 family proteins, their most beneficial application as well as current and future directions in this field are discussed. Targeting Bcl-2 family proteins using SMI strategies is gaining momentum, with the emergence of certain new classes of inhibitors in Phase I and II clinical settings. In view of the tremendous progress toward the development of such inhibitors, this innovative approach certainly holds promise and has the potential to become a future mainstay for cancer therapy. The stage is set for the next generation of SMIs, for not only Bcl-2 proteins but also for Mcl-1. Other emerging molecules in the apoptotic machinery will also be explored and targeted.
Author Sarkar, Fazlul H
Azmi, Asfar S
Philip, Philip A
Mohammad, Ramzi M
Wang, Zhiwei
Author_xml – sequence: 1
  givenname: Asfar S
  surname: Azmi
  fullname: Azmi, Asfar S
  organization: Wayne State University School of Medicine, 740 Hudson Webber Cancer Research Center, Barbara Ann Karmanos Cancer Institute, Department of Pathology, 4100 John R, Detroit, MI 48201, USA
– sequence: 2
  givenname: Zhiwei
  surname: Wang
  fullname: Wang, Zhiwei
– sequence: 3
  givenname: Philip A
  surname: Philip
  fullname: Philip, Philip A
– sequence: 4
  givenname: Ramzi M
  surname: Mohammad
  fullname: Mohammad, Ramzi M
– sequence: 5
  givenname: Fazlul H
  surname: Sarkar
  fullname: Sarkar, Fazlul H
BackLink https://www.ncbi.nlm.nih.gov/pubmed/20812891$$D View this record in MEDLINE/PubMed
BookMark eNo1jstKAzEUQIMo9qF_IJIfmJp7J69ZamlVKHRT1yXJ3LQjnUzJxIV_b0FdHTiLw5mx6zQkYuwBxAIUmCeQBi2CXKC4KAUKQVyxKRgpK6OxnrDZOH4KgVoZecsmKCygbWDK1KqnfOjSgb-EU4W8S8fOd2XII49D5uVIvGRypadU-BB5cClQvmM30Z1Guv_jnH2sV7vlW7XZvr4vnzdVuAyVyjlQyocmemGsC1G01lKLBpxEpa0nr1qNXgmSFqBxZIDqGHSsvSTRAM7Z42_3_OV7avfn3PUuf-____EHzj1HPw
CitedBy_id crossref_primary_10_14348_molcells_2016_2243
crossref_primary_10_1016_j_coph_2011_04_013
crossref_primary_10_1016_j_compbiolchem_2018_03_003
crossref_primary_10_1007_s00066_014_0600_x
crossref_primary_10_1016_j_cbpa_2011_05_024
crossref_primary_10_1007_s11033_024_09254_6
crossref_primary_10_18632_oncotarget_23069
crossref_primary_10_1177_107327481602300203
crossref_primary_10_3390_antiox11061074
crossref_primary_10_1039_C5MD00582E
crossref_primary_10_3390_cancers13020197
crossref_primary_10_5301_jbm_5000116
crossref_primary_10_1007_s00280_012_1995_7
crossref_primary_10_1111_jop_12020
crossref_primary_10_1016_j_ygyno_2022_01_021
crossref_primary_10_1002_jcb_24704
crossref_primary_10_1002_ijc_29509
crossref_primary_10_1007_s00894_024_05901_8
crossref_primary_10_1007_s10620_012_2395_x
crossref_primary_10_1007_s40610_020_00129_w
crossref_primary_10_1016_j_taap_2012_03_007
crossref_primary_10_1371_journal_pone_0106571
crossref_primary_10_1371_journal_pone_0056369
crossref_primary_10_1101_gad_215871_113
crossref_primary_10_1016_j_ejps_2019_04_005
crossref_primary_10_3390_cancers3010001
crossref_primary_10_3892_etm_2018_6865
crossref_primary_10_3892_mmr_2019_10114
crossref_primary_10_1016_j_drudis_2017_05_001
crossref_primary_10_1002_ijc_35157
crossref_primary_10_18632_oncotarget_3868
crossref_primary_10_3760_cma_j_issn_0366_6999_20123391
crossref_primary_10_3390_cancers3021527
crossref_primary_10_1016_j_ejmech_2012_09_012
crossref_primary_10_1016_j_bmc_2012_02_022
crossref_primary_10_14233_ajomc_2022_AJOMC_P384
crossref_primary_10_1002_jcp_28000
crossref_primary_10_1038_ncomms11190
crossref_primary_10_1158_0008_5472_CAN_12_1118
crossref_primary_10_2174_1389557522666220113122117
crossref_primary_10_1042_BSR20192372
crossref_primary_10_4155_ppa_12_41
crossref_primary_10_1002_cncr_26195
crossref_primary_10_1182_blood_2012_06_437624
crossref_primary_10_18632_oncotarget_5342
crossref_primary_10_1158_0008_5472_CAN_14_1849
crossref_primary_10_1158_2326_6066_CIR_23_1001
crossref_primary_10_4161_15384047_2014_986997
crossref_primary_10_1111_his_12076
crossref_primary_10_1039_D2MD00023G
crossref_primary_10_1098_rsif_2013_0860
crossref_primary_10_1097_PAI_0000000000000185
crossref_primary_10_1002_jcp_26015
crossref_primary_10_4155_fmc_11_177
crossref_primary_10_1371_journal_pone_0052483
crossref_primary_10_58600_eurjther1951
crossref_primary_10_1016_j_semcancer_2013_08_008
crossref_primary_10_3892_ijo_2016_3758
crossref_primary_10_1038_cddis_2013_248
crossref_primary_10_1002_psc_3385
crossref_primary_10_1088_1755_1315_743_1_012067
crossref_primary_10_1016_j_ejmech_2014_07_044
crossref_primary_10_1016_j_biopha_2013_09_006
crossref_primary_10_1002_biof_1098
crossref_primary_10_1016_j_msec_2019_110386
crossref_primary_10_1111_febs_13955
crossref_primary_10_1007_s12038_018_9834_6
crossref_primary_10_1186_1471_2407_12_541
crossref_primary_10_1016_j_semcancer_2015_03_001
crossref_primary_10_1016_j_cbi_2016_03_006
crossref_primary_10_1177_1098612X12451404
crossref_primary_10_1186_1476_4598_12_42
crossref_primary_10_3748_wjg_v20_i41_15275
crossref_primary_10_1021_acs_jmedchem_9b01310
crossref_primary_10_1124_jpet_118_251694
crossref_primary_10_18632_aging_204207
crossref_primary_10_3390_v6041837
crossref_primary_10_3390_cancers14020279
crossref_primary_10_3390_md16040123
crossref_primary_10_1016_S0716_8640_13_70659_X
crossref_primary_10_1158_1535_7163_MCT_13_0058
crossref_primary_10_1016_j_jcis_2018_05_033
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
DOI 10.1517/14728214.2010.515210
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
DatabaseTitleList MEDLINE
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
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Economics
EISSN 1744-7623
ExternalDocumentID 20812891
Genre Journal Article
Review
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: NCI NIH HHS
  grantid: 5R01CA131151
– fundername: NCI NIH HHS
  grantid: R01 CA109389
– fundername: NCI NIH HHS
  grantid: R01CA109389
– fundername: NCI NIH HHS
  grantid: R01 CA131151
– fundername: NCI NIH HHS
  grantid: 5R01CA132794
– fundername: NCI NIH HHS
  grantid: R01 CA132794
GroupedDBID ---
00X
03L
0R~
0VX
29G
4.4
53G
5GY
AAMIU
AAOUU
AAPWH
ABBAB
ABEIZ
ABJNI
ABJYH
ABLIJ
ABLKL
ABXYU
ACGFS
ACIEZ
ADCVX
ADRBQ
ADTOD
AECIN
AENEX
AEOZL
AFRVT
AGDLA
AGMHR
AGMLL
AIJEM
AIRBT
AIYSM
AKBVH
ALMA_UNASSIGNED_HOLDINGS
ALQZU
BABNJ
BLEHA
CAZVN
CCCUG
CGR
CS3
CUY
CVF
DASJU
DAWQK
DKSSO
DU5
EBS
ECM
EIF
EJD
EMOBN
F5P
H13
HZ~
KRBQP
KSSTO
KUULJ
KWAYT
KYCEM
LJTGL
M44
M4Z
MK0
NPM
O9-
RNANH
TASJS
TBQAZ
TDBHL
TERGH
TFDNU
TFL
TFW
TUROJ
TZHSB
V1S
~1N
ID FETCH-LOGICAL-c472t-aa155bc9fb078acf0d88ed271a42568beb5d62b50e48119ae71e3fc6f3b4e0912
IngestDate Mon Jul 21 06:01:16 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c472t-aa155bc9fb078acf0d88ed271a42568beb5d62b50e48119ae71e3fc6f3b4e0912
PMID 20812891
ParticipantIDs pubmed_primary_20812891
PublicationCentury 2000
PublicationDate 2011-03-01
PublicationDateYYYYMMDD 2011-03-01
PublicationDate_xml – month: 03
  year: 2011
  text: 2011-03-01
  day: 01
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Expert opinion on emerging drugs
PublicationTitleAlternate Expert Opin Emerg Drugs
PublicationYear 2011
SSID ssj0026574
Score 2.2139158
SecondaryResourceType review_article
Snippet Bcl-2 family proteins are a component of the antiapoptotic machinery and are overexpressed in different malignancies. Accordingly, their enhanced expression...
SourceID pubmed
SourceType Index Database
StartPage 59
SubjectTerms Antineoplastic Agents - administration & dosage
Antineoplastic Agents - adverse effects
Antineoplastic Agents - therapeutic use
Apoptosis - drug effects
Clinical Trials as Topic
Disease-Free Survival
Drug Discovery - methods
Humans
Neoplasms - drug therapy
Neoplasms - metabolism
Neoplasms - pathology
Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors
Small Molecule Libraries - administration & dosage
Small Molecule Libraries - adverse effects
Small Molecule Libraries - therapeutic use
Treatment Outcome
Title Emerging Bcl-2 inhibitors for the treatment of cancer
URI https://www.ncbi.nlm.nih.gov/pubmed/20812891
Volume 16
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3Pa9swFBZLd-guo93WdT_RYbeiNLIl2T5mY6MMssNIWNklSLJEDLUTkpRB_vo9SXbUphltdzHBCkLR-_zyvc_vPSH0yeTwtyZ1SUShLGGllSTnRpNUMWuEzFLra2FGP8TFhH2_5JdRyvbVJWvV15u9dSX_Y1W4B3Z1VbKPsOx2UrgBn8G-cAULw_VBNnaKkj9k6LO-IslZ1cwqVfnjc7rkwZhH7tLHnYWXt7R41-gYxhZV44ljc2a6KcvldZTQh5vav_UfrqxcRrX0Vys2_55Vf0x18wVDtYhqTZRLR_OZrOsAqp-y3lStFltGGbVLu-qb4Ckzxgh40vSWKxV3IBP8Yuj6fcddcxoK_jMI_CgLiXbcMYrBza_Dpi9qb8IECAxEiPT-0Z0m2t1QD_UgnHDnozpRp43LBc9YW1UJCzrftxzXM7qdYif-8DxkfISetwEEHgY0HKMnpnmBDrv68tVLxDtUYI8KHFGBARUYUIG3qMBziwMqXqHJt6_jLxekPRyDaFjfmkgJTFDpwiogeVLbQZnnpkwyKsELi1wZxUuRKD4wLKe0kCajJrVaWHgKDZDE5AQdNPPGnCJMxcAqT_R0wVimpTK5KgS1hc1szvgb9Dr84ukidECZdnvx9p8j79CzCJv36KmFR858AP62Vh_97v8Fh0ZBWw
linkProvider National Library of Medicine
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=Emerging+Bcl-2+inhibitors+for+the+treatment+of+cancer&rft.jtitle=Expert+opinion+on+emerging+drugs&rft.au=Azmi%2C+Asfar+S&rft.au=Wang%2C+Zhiwei&rft.au=Philip%2C+Philip+A&rft.au=Mohammad%2C+Ramzi+M&rft.date=2011-03-01&rft.eissn=1744-7623&rft.volume=16&rft.issue=1&rft.spage=59&rft_id=info:doi/10.1517%2F14728214.2010.515210&rft_id=info%3Apmid%2F20812891&rft_id=info%3Apmid%2F20812891&rft.externalDocID=20812891