Evidence map›Paper›PMID 22509329›Full record

ArticlePloS one2012

Thrombospondin-1 type 1 repeats in a model of inflammatory bowel disease: transcript profile and therapeutic effects.

Zenaida P Lopez-Dee, Sridar V Chittur, Bhumi Patel, Rebecca Stanton, Michelle Wakeley, Brittany Lippert, Anastasya Menaker, Bethany Eiche, Robert Terry, Linda S Gutierrez

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Thrombospondin 1 in Metabolic Diseases.Frontiers in endocrinology · 2021
    Review
  9. Article
  10. Article
  11. Integration of pro- and anti-angiogenic signals by endothelial cells.Journal of cell communication and signaling · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Angiogenesis in Inflammatory Bowel Disease.International journal of inflammation · 2015
    Review
  16. Article
  17. 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

10 authors at 2 institutions in 1 country.

Zenaida P Lopez-DeeDepartment of Biology, Wilkes University, Wilkes-Barre, Pennsylvania, United States of America.
Sridar V Chittur
Bhumi Patel
Rebecca Stanton
Michelle Wakeley
Brittany Lippert
Anastasya Menaker
Bethany Eiche
Robert Terry
Linda S Gutierrez
Wilkes University · USUniversity at Albany, State University of New York · US

Funding

Thrombospondin in ulceractive colitis and carcinogenesisR15DK067901 · NIDDK · WILKES UNIVERSITY · PI GUTIERREZ, LINDA S · 2006 to 2010
$443k
Howard Hughes Medical Institute 52006328NIDDK NIH HHS DK067901-12 02NIDDK NIH HHS R15 DK067901
6 · The paper itself

Abstract

Thrombospondin-1 (TSP-1) is a matricellular protein with regulatory functions in inflammation and cancer. The type 1 repeats (TSR) domains of TSP-1 have been shown to interact with a wide range of proteins that result in the anti-angiogenic and anti-tumor properties of TSP-1. To ascertain possible functions and evaluate potential therapeutic effects of TSRs in inflammatory bowel disease, we conducted clinical, histological and microarray analyses on a mouse model of induced colitis. We used dextran sulfate sodium (DSS) to induce colitis in wild-type (WT) mice for 7 days. Simultaneously, mice were injected with either saline or one form of TSP-1 derived recombinant proteins, containing either (1) the three type 1 repeats of the TSP-1 (3TSR), (2) the second type 1 repeat (TSR2), or (3) TSR2 with the RFK sequence (TSR2+RFK). Total RNA isolated from the mice colons were processed and hybridized to mouse arrays. Array data were validated by real-time qPCR and immunohistochemistry. Histological and disease indices reveal that the mice treated with the TSRs show different patterns of leukocytic infiltration and that 3TSR treatment was the most effective in decreasing inflammation in DSS-induced colitis. Transcriptional profiling revealed differentially expressed (DE) genes, with the 3TSR-treated mice showing the least deviation from the WT-water controls. In conclusion, this study shows that 3TSR treatment is effective in attenuating the inflammatory response to DSS injury. In addition, the transcriptomics work unveils novel genetic data that suggest beneficial application of the TSR domains in inflammatory bowel disease.

Indexed as

Repetitive Sequences, Amino AcidAnimalsApoptosisCell AdhesionColitisDextran SulfateDisease Models, AnimalInflammatory Bowel DiseasesLeukocytesMiceNeoplasmsNeovascularization, PathologicProtein Structure, TertiaryReal-Time Polymerase Chain ReactionRecombinant ProteinsRNA, MessengerDextran SulfateRecombinant ProteinsRNA, MessengerThrombospondin 1

Identifiers

PMID22509329
PMCPMC3318003
OpenAlexW2080107580

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.