Evidence map›Paper›PMID 20812891›Full record

ReviewExpert opinion on emerging drugs2011

Emerging Bcl-2 inhibitors for the treatment of cancer.

Asfar S Azmi, Zhiwei Wang, Philip A Philip, Ramzi M Mohammad, Fazlul H Sarkar

Abstract readReview
In one paragraph

Review in Expert opinion on emerging drugs, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 101 citations in OpenAlex.

  1. Pleiotropic Effects of 3-International journal of molecular sciences · 2026
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  18. Oncotarget · 2018
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Asfar S AzmiWayne 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.
Zhiwei Wang
Philip A Philip
Ramzi M Mohammad
Fazlul H Sarkar
The Barbara Ann Karmanos Cancer Institute · USWayne State University · US

Funding

RO1: A novel and targeted approach to inhibit invasion and angiogenesisR01CA131151 · NCI · WAYNE STATE UNIVERSITY · PI SARKAR, FAZLUL H. · 2008 to 2012
$1.8M
FoxM1: A molecular target in pancreatic cancerR01CA132794 · NCI · WAYNE STATE UNIVERSITY · PI SARKAR, FAZLUL H. · 2009 to 2013
$1.5M
Specific Targets for Pancreatic Cancer TherapyR01CA109389 · NCI · WAYNE STATE UNIVERSITY · PI MOHAMMAD, RAMZI M. · 2007 to 2011
$1.2M
NCI NIH HHS 5R01CA131151NCI NIH HHS 5R01CA132794NCI NIH HHS R01 CA109389NCI NIH HHS R01CA109389NCI NIH HHS R01 CA131151NCI NIH HHS R01 CA132794
6 · The paper itself

Abstract

introductionBcl-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. AREAS COVERED: 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. EXPERT OPINION: 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.

Indexed as

Antineoplastic AgentsApoptosisClinical Trials as TopicDisease-Free SurvivalDrug DiscoveryHumansNeoplasmsProto-Oncogene Proteins c-bcl-2Small Molecule LibrariesTreatment OutcomeAntineoplastic AgentsProto-Oncogene Proteins c-bcl-2Small Molecule Libraries

Identifiers

PMID20812891
PMCPMC3084453
OpenAlexW2128447926

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.