Evidence map›Paper›PMID 20001556›Full record

ReviewExpert opinion on investigational drugs2010

Targeting the transforming growth factor-beta signaling pathway in human cancer.

Nagathihalli S Nagaraj, Pran K Datta

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on investigational drugs, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed
4.8field-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

139 citing papers in PubMed, 263 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. The Role ofInternational journal of molecular sciences · 2023
    Article
  13. Article
  14. Targeting Myc-driven stress addiction in colorectal cancer.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2023
    Review
  15. Review
  16. Review
  17. Suppression of CD56Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  18. Article
  19. Review
  20. Article

79 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

2 authors at 2 institutions in 1 country.

Nagathihalli S NagarajVanderbilt University School of Medicine, Vanderbilt-Ingram Cancer Center, Department of Surgery, Nashville, TN 37232, USA.
Pran K Datta
Vanderbilt-Ingram Cancer CenterVanderbilt University · US

Funding

TARGETING NOTCH 3 IN LUNG CANCERP50CA090949 · NCI · VANDERBILT UNIVERSITY · PI MASSION, PIERRE P. · 2001 to 2011
$24.1M
STRAP and Smad 7 Signaling in Colorectal CarcinomasR01CA095195 · NCI · VANDERBILT UNIVERSITY · PI DATTA, PRAN K · 2003 to 2013
$2.4M
Targeting TGF-beta Signaling in Lung CancerR01CA113519 · NCI · VANDERBILT UNIVERSITY · PI DATTA, PRAN K · 2006 to 2010
$1.2M
NCI NIH HHS 5P50CA90949NCI NIH HHS CA113519NCI NIH HHS P50 CA090949NCI NIH HHS R01 CA095195NCI NIH HHS R01 CA113519NCI NIH HHS R01 CA95195
6 · The paper itself

Abstract

The transforming growth factor-ss (TGF-beta) signaling pathway plays a pivotal role in diverse cellular processes. TGF-beta switches its role from a tumor suppressor in normal or dysplastic cells to a tumor promoter in advanced cancers. It is widely believed that the Smad-dependent pathway is involved in TGF-beta tumor-suppressive functions, whereas activation of Smad-independent pathways, coupled with the loss of tumor-suppressor functions of TGF-beta, is important for its pro-oncogenic functions. TGF-beta signaling has been considered a useful therapeutic target. The discovery of oncogenic actions of TGF-beta has generated a great deal of enthusiasm for developing TGF-beta signaling inhibitors for the treatment of cancer. The challenge is to identify the group of patients where targeted tumors are not only refractory to TGF-beta-induced tumor suppressor functions but also responsive to the tumor-promoting effects of TGF-beta. TGF-beta pathway inhibitors, including small and large molecules, have now entered clinical trials. Preclinical studies with these inhibitors have shown promise in a variety of different tumor models. Here, we focus on the mechanisms of signaling and specific targets of the TGF-beta pathway that are critical effectors of tumor progression and invasion. This report also examines the therapeutic intervention of TGF-ss signaling in human cancers.

Indexed as

Antineoplastic AgentsClinical Trials as TopicDrug DiscoveryHumansNeoplasmsOligonucleotides, AntisenseSignal TransductionSmall Molecule LibrariesTransforming Growth Factor betaAntineoplastic AgentsOligonucleotides, AntisenseSmall Molecule LibrariesTransforming Growth Factor beta

Identifiers

PMID20001556
PMCPMC2796203
OpenAlexW2132997519

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.