Evidence map›Paper›PMID 22652457›Full record

ArticleExperimental cell research2012

The hypoxia-inducible factor-responsive proteins semaphorin 4D and vascular endothelial growth factor promote tumor growth and angiogenesis in oral squamous cell carcinoma.

Hua Zhou, Ying-Hua Yang, Nada O Binmadi, Patrizia Proia, John R Basile

Open access · greenAbstract read
In one paragraph

Article in Experimental cell research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  4. SEMAPHORINS and their receptors: focus on the crosstalk between melanoma and hypoxia.Journal of experimental & clinical cancer research : CR · 2021
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  18. Semaphorins and plexins as therapeutic targets.Nature reviews. Drug discovery · 2014
    Review
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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 3 countries.

Hua ZhouDepartment of Oncology and Diagnostic Sciences, University of Maryland Dental School, Baltimore, MD 21201, USA.
Ying-Hua Yang
Nada O Binmadi
Patrizia Proia
John R Basile
University of Maryland, Baltimore · USKing Abdulaziz University · SA

Funding

The Role of Semaphorin 4D and Plexin-B1 in Tumor-Induced Angiogenesis.R01CA133162 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI BASILE, JOHN R. · 2009 to 2013
$1.5M
NCI NIH HHS R01 CA133162NCI NIH HHS R01-CA133162
6 · The paper itself

Abstract

Growth and metastasis of solid tumors requires induction of angiogenesis to ensure the delivery of oxygen, nutrients and growth factors to rapidly dividing transformed cells. Through either mutations, hypoxia generated by cytoreductive therapies, or when a malignancy outgrows its blood supply, tumor cells undergo a change from an avascular to a neovascular phenotype, a transition mediated by the hypoxia-inducible factor (HIF) family of transcriptional regulators. Vascular endothelial growth factor (VEGF) is one example of a gene whose transcription is stimulated by HIF. VEGF plays a crucial role in promoting tumor growth and survival by stimulating new blood vessel growth in response to such stresses as chemotherapy or radiotherapy-induced hypoxia, and it therefore has become a tempting target for neutralizing antibodies in the treatment of advanced neoplasms. Emerging evidence has shown that the semaphorins, proteins originally associated with control of axonal growth and immunity, are regulated by changes in oxygen tension as well and may play a role in tumor-induced angiogenesis. Through the use of RNA interference, in vitro and in vivo angiogenesis assays and tumor xenograft experiments, we demonstrate that expression of semaphorin 4D (SEMA4D), which is under the control of the HIF-family of transcription factors, cooperates with VEGF to promote tumor growth and vascularity in oral squamous cell carcinoma (OSCC). We use blocking antibodies to show that targeting SEMA4D function along with VEGF could represent a novel anti-angiogenic therapeutic strategy for the treatment of OSCC and other solid tumors.

Indexed as

AnimalsAntigens, CDCarcinoma, Squamous CellCell ProliferationCells, CulturedHEK293 CellsHumansMiceMouth NeoplasmsNeoplasms, ExperimentalNeovascularization, PathologicSemaphorinsVascular Endothelial Growth Factor AAntigens, CDCD100 antigenSemaphorinsVascular Endothelial Growth Factor A

Identifiers

PMID22652457
PMCPMC3389129
OpenAlexW1983256377

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.