Evidence map›Paper›PMID 18855619›Full record

ReviewCurrent drug targets2008

Thrombospondin and apoptosis: molecular mechanisms and use for design of complementation treatments.

Y Mirochnik, A Kwiatek, O V Volpert

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Current drug targets, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02551042 (A Phase II, Double-blind, Randomized, Placebo-controlled Study to Investigate Pharmacokinetics), which is not on this map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
1.8field-weighted citation impact, top 16% 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.

NCT02551042 phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Phase II, Double-blind, Randomized, Placebo-controlled Study to Investigate Pharmacokinetics (PK), Safety and Efficacy of Intravenous Factor XIII Treatment in Patients With Systemic Sclerosis

TypeinterventionalSponsorUniversity College, LondonRan2015 to 2018Enrolled26ConditionsSystemic SclerosisArmsFibrogammin®P, coagulation factor XIII concentrate (Human), 0.9% sodium chloride
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 100 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Thrombospondin-2 as a diagnostic biomarker for distal cholangiocarcinoma and pancreatic ductal adenocarcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Thrombospondin 1 and Its Diverse Roles as a Regulator of Extracellular Matrix in Fibrotic Disease.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2019
    Review
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

3 authors at 2 institutions in 2 countries.

Y MirochnikDepartment of Urology, Feinberg School of Medicine, Northwestern University, 303 East Chicago Avenue, Tarry 16-703 Chicago, IL 60611-3008, USA.
A Kwiatek
O V Volpert
Northwestern University · USCentre for Cancer Biology · AU

Funding

Regulation of angiogenic balance by thrombospondin-1.R01HL068033 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI VOLPERT, OLGA VALERY · 2001 to 2009
$2.6M
Maximization of anti-angiogenesis by thrombospondin-1R01HL077471 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI VOLPERT, OLGA VALERY · 2005 to 2008
$1.1M
NHLBI NIH HHS R01 HL068033NHLBI NIH HHS R01 HL077471
6 · The paper itself

Abstract

Thrombospondin-1 is the first and most studied naturally occurring protein inhibitor of angiogenesis. Its characteristic multi-domain structure determines thrombospondin-1 divergent functions, which include but are not limited to the regulation of angiogenesis. Below we overview the structural determinants and receptors expressed on the endothelial and other cell types, that are at the root of thrombospondin-1 striking ability to block neovascularization. We specifically emphasize thrombospondin-1 direct apoptotic action on the remodeling vascular endothelium and summarize current knowledge of its pro-apoptotic signaling and transcriptional networks. Further, we provide comprehensive survey of the thrombospondin-based anti-angiogenic strategies with special focus on the combination treatments. We convincingly illustrate how precise knowledge of the pro-apoptotic events and intermediates elicited by thrombospondin in the vascular endothelial cells facilitates the design of the most effective treatment combinations, where the efficacy of thrombospondin-derived compounds is maximized by the partner drug(s) ("complementation" strategies) and provide examples of such fine-tuning of the thrombospondin-based anti-angiogenic treatments.

Indexed as

Drug DesignAmino Acid SequenceAngiogenesis InhibitorsAnimalsApoptosisDrug Therapy, CombinationHumansMolecular Sequence DataPeptide FragmentsThrombospondinsAngiogenesis InhibitorsPeptide FragmentsThrombospondins

Identifiers

PMID18855619
PMCPMC2853770
OpenAlexW2104423020

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.