Evidence map›Paper›PMID 27761803›Full record

ArticleJournal of cell communication and signaling2017

The pivotal role of CCN2 in mammalian palatogenesis.

Joseph T Tarr, Timothy G Visser, Joanne E Moon, Honey Hendesi, Mary F Barbe, James P Bradley, Steven N Popoff

Open access · greenAbstract read
In one paragraph

Article in Journal of cell communication and signaling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Joseph T TarrDepartment of Anatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, 3500 N. Broad St. Suite 440, Philadelphia, PA, 19140, USA.
Timothy G VisserDepartment of Anatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, 3500 N. Broad St. Suite 440, Philadelphia, PA, 19140, USA.
Joanne E MoonDepartment of Anatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, 3500 N. Broad St. Suite 440, Philadelphia, PA, 19140, USA.
Honey HendesiDepartment of Anatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, 3500 N. Broad St. Suite 440, Philadelphia, PA, 19140, USA.
Mary F BarbeDepartment of Anatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, 3500 N. Broad St. Suite 440, Philadelphia, PA, 19140, USA.
James P BradleyDepartment of General Surgery, Division of Plastic and Reconstructive Surgery, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, 19140, USA.
Steven N PopoffDepartment of Anatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, 3500 N. Broad St. Suite 440, Philadelphia, PA, 19140, USA. spopoff@temple.edu.
Temple University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mammalian palatogenesis is a complex process involving a temporally and spatially regulated myriad of factors. Together these factors control the 3 vital processes of proliferation, elevation and fusion of the developing palate. In this study, we show for the first time the unequivocally vital role of CCN2 in development of the mammalian palate. We utilized CCN2 knockout (KO) mice and cranial neural crest derived mesenchymal cells from these CCN2 KO mice to investigate the 3 processes crucial to normal palatogenesis. Similar to previously published reports, the absence of CCN2 inhibits proliferation of cells in the palate specifically at the G1/S transition. Absence of CCN2 also inhibited palatal shelf elevation from the vertical to horizontal position. CCN2 KO mesenchymal cells demonstrated deficiencies in adhesion and spreading owing to an inability to activate Rac1 and RhoA. On the contrary, CCN2 KO mesenchymal cells exhibited increased rates of migration compared to WT cells. The addition of exogenous CCN2 to KO mesenchymal cells restored their ability to spread normally on fibronectin. Finally, utilizing an organ culture model we show that the palatal shelves of the CCN2 KO mice demonstrate an inability to fuse when apposed. Together, these data signify that CCN2 plays an indispensible role in normal development of the mammalian palate and warrants additional studies to determine the precise mechanism(s) responsible for these effects.

Indexed as

CCN2Cranial neural crestPalate elevationPalate fusionPalatogenesisProliferation

Identifiers

PMID27761803
PMCPMC5362573
OpenAlexW2535519901

What OpenQuestion holds

Textmetadata
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.