Evidence map›Paper›PMID 22249026›Full record

ReviewThe international journal of biochemistry & cell biology2012

Diverse biological functions of the SPARC family of proteins.

Amy D Bradshaw

Open access · greenAbstract readReview
In one paragraph

Review in The international journal of biochemistry & cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed, 2 pooled it
13.0field-weighted citation impact, top 1% 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

145 citing papers in PubMed, 2 syntheses or guidelines pooled it, 262 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Teneurins Are SPARCL1 Receptors.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Expression of MIR155HG, LOC283856, KIAA0125, and LOC100190986 as potential prognostic and predictive biomarkers for breast cancer.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 2026
    Article
  15. Review
  16. Article
  17. Article
  18. Regulatory Mechanisms of SPARC Overexpression in Melanoma Progression.International journal of molecular sciences · 2025
    Article
  19. Article
  20. The life cycle of type IV collagen.Matrix biology : journal of the International Society for Matrix Biology · 2025
    Review

85 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

1 author at 1 institution in 1 country.

Amy D BradshawDivision of Cardiology, Department of Medicine, Medical University of South Carolina and Ralph H. Johnson Veteran's Administration, Charleston, SC, United States. bradshad@musc.edu
Ralph H. Johnson VA Medical Center · US

Funding

Post-Synthetic Procollagen Processing in Load-Induced Left Ventricular RemodelingR01HL094517 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADSHAW, AMY D · 2009 to 2010
$738k
NHLBI NIH HHS R01 HL094517Wellcome Trust 094517
6 · The paper itself

Abstract

The SPARC family of proteins represents a diverse group of proteins that modulate cell interaction with the extracellular milieu. The eight members of the SPARC protein family are modular in nature. Each shares a follistatin-like domain and an extracellular calcium binding E-F hand motif. In addition, each family member is secreted into the extracellular space. Some of the shared activities of this family include, regulation of extracellular matrix assembly and deposition, counter-adhesion, effects on extracellular protease activity, and modulation of growth factor/cytokine signaling pathways. Recently, several SPARC family members have been implicated in human disease pathogenesis. This review discusses recent advances in the understanding of the functional roles of the SPARC family of proteins in development and disease.

Indexed as

AnimalsCell AdhesionCytokinesEF Hand MotifsExtracellular Matrix ProteinsFollistatinHumansIntercellular Signaling Peptides and ProteinsNeoplasmsNeovascularization, PathologicOsteonectinProtein FoldingProtein MultimerizationCytokinesExtracellular Matrix ProteinsFollistatinIntercellular Signaling Peptides and ProteinsOsteonectin

Identifiers

PMID22249026
PMCPMC3312742
OpenAlexW2034264001

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.