Evidence map›Paper›PMID 31243391›Full record

ReviewNature reviews. Cardiology2019

Vascular smooth muscle cells in atherosclerosis.

Gemma L Basatemur, Helle F Jørgensen, Murray C H Clarke, Martin R Bennett, Ziad Mallat

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cardiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 641 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
641citing papers in PubMed, 1 pooled it
41.7field-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

641 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,050 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Phenotypic switching of gastrointestinal smooth muscle cells and the regulatory role of macrophages: a literature review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  10. Review
  11. Article
  12. Article
  13. Olfactomedin-2 at the Crossroads of Smooth Muscle Cell Plasticity.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Article
  14. Olfactomedin 2 Promotes Atherosclerosis by Eliciting Smooth Muscle Foam Cell Formation.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Article
  15. HMGB1 as a danger signal in vascular remodeling.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2026
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. USP5 Stabilizes TGFBR1 to Drive Vascular Smooth Muscle Cell Senescence and Atherosclerosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article

581 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

5 authors at 2 institutions in 2 countries.

Gemma L BasatemurDivision of Cardiovascular Medicine, Department of Medicine, University of Cambridge, Cambridge, UK.
Helle F JørgensenDivision of Cardiovascular Medicine, Department of Medicine, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-7909-2977
Murray C H ClarkeDivision of Cardiovascular Medicine, Department of Medicine, University of Cambridge, Cambridge, UK.
Martin R BennettDivision of Cardiovascular Medicine, Department of Medicine, University of Cambridge, Cambridge, UK.
Ziad MallatDivision of Cardiovascular Medicine, Department of Medicine, University of Cambridge, Cambridge, UK. zm255@medschl.cam.ac.uk.ORCID http://orcid.org/0000-0003-0443-7878
University of Cambridge · GBDélégation Paris 5 · FR

Funding

British Heart Foundation FS/09/005/26845British Heart Foundation FS/13/29/30024British Heart Foundation FS/13/3/30038British Heart Foundation FS/15/38/31516British Heart Foundation FS/18/19/33371British Heart Foundation PG/11/112/29272British Heart Foundation PG/12/86/29930British Heart Foundation PG/13/25/30014British Heart Foundation PG/16/11/32021British Heart Foundation PG/16/63/32307British Heart Foundation PG/17/9/32834British Heart Foundation PG/19/6/34153British Heart Foundation RG/13/14/30314British Heart Foundation RG/16/8/32388Medical Research Council G0800784Medical Research Council G1000847
6 · The paper itself

Abstract

Vascular smooth muscle cells (VSMCs) are a major cell type present at all stages of an atherosclerotic plaque. According to the 'response to injury' and 'vulnerable plaque' hypotheses, contractile VSMCs recruited from the media undergo phenotypic conversion to proliferative synthetic cells that generate extracellular matrix to form the fibrous cap and hence stabilize plaques. However, lineage-tracing studies have highlighted flaws in the interpretation of former studies, revealing that these studies had underestimated both the content and functions of VSMCs in plaques and have thus challenged our view on the role of VSMCs in atherosclerosis. VSMCs are more plastic than previously recognized and can adopt alternative phenotypes, including phenotypes resembling foam cells, macrophages, mesenchymal stem cells and osteochondrogenic cells, which could contribute both positively and negatively to disease progression. In this Review, we present the evidence for VSMC plasticity and summarize the roles of VSMCs and VSMC-derived cells in atherosclerotic plaque development and progression. Correct attribution and spatiotemporal resolution of clinically beneficial and detrimental processes will underpin the success of any therapeutic intervention aimed at VSMCs and their derivatives.

Indexed as

AnimalsAtherosclerosisCell PlasticityCell ProliferationCellular SenescenceDisease ProgressionExtracellular MatrixHumansMyocytes, Smooth MusclePhenotypePlaque, Atherosclerotic

Identifiers

PMID31243391
OpenAlexW2955108563

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.