Evidence map›Paper›PMID 20941592›Full record

ReviewCurrent topics in microbiology and immunology2011

Small-molecule inhibitors reveal a new function for Bcl-2 as a proangiogenic signaling molecule.

Benjamin D Zeitlin, Jacques E Nör

Abstract readReview
In one paragraph

Review in Current topics in microbiology and immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
4.7field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Inhibitor of MYC identified in a Kröhnke pyridine library.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  4. Review
  5. Article
  6. Article
  7. Article
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

2 authors at 2 institutions in 1 country.

Benjamin D ZeitlinDepartment of Restorative Sciences, University of Michigan School of Dentistry, Ann Arbor, MI, USA.
Jacques E Nör
Michigan Center for Translational Pathology · USUniversity of Michigan–Ann Arbor · US

Funding

Therapeutic Potential and Mechanism of Action of Potent Small Molecule InhibitorsP50CA097248 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WOLF, GREGORY T · 2002 to 2013
$25.3M
Bcl-2 /CXC Chemokines in Head /Neck Tumor AngiogenesisR01DE015948 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NOR, JACQUES EDUARDO · 2004 to 2008
$1.9M
Therapeutic Inhibition of Bcl-2 and Head & Neck Tumor AngiogenesisR01DE016586 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NOR, JACQUES EDUARDO · 2005 to 2009
$1.7M
Neovascular Regression for Oral Cancer TherapyR01DE014601 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NOR, JACQUES EDUARDO · 2002 to 2006
$1.3M
Endothelial and head & neck cancer stem cell crosstalks and resistance to therapyR21DE019279 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NOR, JACQUES EDUARDO · 2008 to 2009
$419k
NCI NIH HHS P50 CA097248NCI NIH HHS P50-CA97248NIDCR NIH HHS R01 DE014601NIDCR NIH HHS R01 DE015948NIDCR NIH HHS R01 DE016586NIDCR NIH HHS R01-DE14601NIDCR NIH HHS R01-DE15948NIDCR NIH HHS R01-DE16586NIDCR NIH HHS R21 DE019279NIDCR NIH HHS R21-DE19279
6 · The paper itself

Abstract

Cancer has a complex etiology and displays a wide range of cellular escape pathways that allow it to circumvent treatment. Signaling molecules functionally downstream of the circumvented pathways, and particularly at checkpoints where several of these pathways intersect, provide valuable targets for the development of novel anti-cancer drugs. Bcl-2, a pro-survival signaling molecule, is one such protein. This review examines the efficacy, potency, and function of several small molecule inhibitor drugs targeted to the Bcl-2 family of proteins. The review focuses on the compounds with most available data within the literature and discusses both the anti-cancer and the recently unveiled anti-angiogenic potential of this new class of drugs.

Indexed as

Neovascularization, PathologicAngiogenesis InhibitorsAnimalsApoptosisDrug DiscoveryHumansMitochondriaNeoplasmsProto-Oncogene Proteins c-bcl-2Signal TransductionAngiogenesis InhibitorsProto-Oncogene Proteins c-bcl-2

Identifiers

PMID20941592
PMCPMC3812667
OpenAlexW61805077

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.