Evidence map›Paper›PMID 21851287›Full record

ReviewExpert opinion on investigational drugs2011

Targeting Mcl-1 for the therapy of cancer.

Bridget A Quinn, Rupesh Dash, Belal Azab, Siddik Sarkar, Swadesh K Das, Sachin Kumar, Regina A Oyesanya, Santanu Dasgupta, Paul Dent, Steven Grant and 11 more

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on investigational drugs, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

100 citing papers in PubMed, 207 citations in OpenAlex.

  1. Article
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  15. Review
  16. Article
  17. B Cell Lymphoma 2: A Potential Therapeutic Target for Cancer Therapy.International journal of molecular sciences · 2021
    Review
  18. Article
  19. Article
  20. Review of Venetoclax in CLL, AML and Multiple Myeloma.Journal of personalized medicine · 2021
    Review

40 more citing papers are in PubMed but not listed here.

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

21 authors at 4 institutions in 1 country.

Bridget A QuinnVirginia Commonwealth University, School of Medicine, Department of Human and Molecular Genetics, Richmond, VA, USA. pbfisher@vcu.edu
Rupesh Dash
Belal Azab
Siddik Sarkar
Swadesh K Das
Sachin Kumar
Regina A Oyesanya
Santanu Dasgupta
Paul Dent
Steven Grant
Mohamed Rahmani
David T Curiel
Igor Dmitriev
Michael Hedvat
Jun Wei
Bainan Wu
John L Stebbins
John C Reed
Maurizio Pellecchia
Devanand Sarkar
Paul B Fisher
Virginia Commonwealth University · USSanford Burnham Prebys Medical Discovery Institute · USWashington University in St. Louis · USVirginia Commonwealth University Medical Center · US

Funding

SPORE in LymphomaP50CA130805 · NCI · UNIVERSITY OF ROCHESTER · PI FISHER, RICHARD I · 2008 to 2012
$11.7M
P4 -TARGETING MULTIPLE MYELOMA BY COMBINING CDK INHIBITORS AND BCL-2 ANTAGONISTSP50CA142509 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2010 to 2014
$11.1M
Virginia Commonwealth University IRADCAK12GM093857 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DANIEL C BULLARD, John J Ryan · 2010 to 2026
$7.0M
Translational Applications of mda-7/IL-24 in CancerP01CA104177 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI CURIEL, DAVID TERRY · 2005 to 2009
$6.5M
SIGNALING PATHWAYS REGULATING EPITHELIAL CELL SURVIVALR01DK052825 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 1999 to 2013
$3.3M
MDA-7: Novel Cancer Therapeutic GeneR01CA097318 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2002 to 2012
$2.8M
NF-kappaB Inhibitors and Differentiation-Inducers in LeukemiaR01CA093738 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRANT, STEVEN · 2002 to 2011
$2.4M
Interplay between tumor and microenvironment in bone metastasisR01CA259599 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B, WANG, XIANG-YANG SHAWN · 2021 to 2025
$2.3M
Checkpoint Abrogation and MEK 1/2 Inhibition in MyelomaR01CA100866 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRANT, STEVEN · 2003 to 2013
$2.2M
Targeting apoptosis via chemical design of Bcl-2 antagonistsR01CA149668 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PELLECCHIA, MAURIZIO · 2010 to 2014
$1.9M
OSU-03012 therapy for glioblastomaR01CA141703 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 2010 to 2014
$1.5M
Lapatinib and Obatoclax combination therapyR01CA150214 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 2010 to 2014
$1.5M
NCI NIH HHS P01 CA104177NCI NIH HHS P50 CA130805NCI NIH HHS P50 CA142509NCI NIH HHS R01 CA093738NCI NIH HHS R01 CA097318NCI NIH HHS R01 CA100866NCI NIH HHS R01 CA127641NCI NIH HHS R01 CA141703NCI NIH HHS R01 CA149668NCI NIH HHS R01 CA150214NCI NIH HHS R01 CA259599NCI NIH HHS RC2 CA148431NCI NIH HHS RC2CA148431NIDDK NIH HHS R01 DK052825NIGMS NIH HHS K12 GM093857
6 · The paper itself

Abstract

introductionHuman cancers are genetically and epigenetically heterogeneous and have the capacity to commandeer a variety of cellular processes to aid in their survival, growth and resistance to therapy. One strategy is to overexpress proteins that suppress apoptosis, such as the Bcl-2 family protein Mcl-1. The Mcl-1 protein plays a pivotal role in protecting cells from apoptosis and is overexpressed in a variety of human cancers. AREAS COVERED: Targeting Mcl-1 for extinction in these cancers, using genetic and pharmacological approaches, represents a potentially effectual means of developing new efficacious cancer therapeutics. Here we review the multiple strategies that have been employed in targeting this fundamental protein, as well as the significant potential these targeting agents provide in not only suppressing cancer growth, but also in reversing resistance to conventional cancer treatments. EXPERT OPINION: We discuss the potential issues that arise in targeting Mcl-1 and other Bcl-2 anti-apoptotic proteins, as well problems with acquired resistance. The application of combinatorial approaches that involve inhibiting Mcl-1 and manipulation of additional signaling pathways to enhance therapeutic outcomes is also highlighted. The ability to specifically inhibit key genetic/epigenetic elements and biochemical pathways that maintain the tumor state represent a viable approach for developing rationally based, effective cancer therapies.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsDrug DesignHumansMyeloid Cell Leukemia Sequence 1 ProteinNeoplasmsProto-Oncogene Proteins c-bcl-2Antineoplastic AgentsMyeloid Cell Leukemia Sequence 1 ProteinProto-Oncogene Proteins c-bcl-2

Identifiers

PMID21851287
PMCPMC3205956
OpenAlexW2120308617

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.