Evidence map›Paper›PMID 33036489›Full record

ReviewInternational journal of molecular sciences2020

Therapeutic Potential of Endothelial Colony-Forming Cells in Ischemic Disease: Strategies to Improve their Regenerative Efficacy.

Pawan Faris, Sharon Negri, Angelica Perna, Vittorio Rosti, Germano Guerra, Francesco Moccia

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The Epigenetic Landscape of Hemophilia.Current molecular medicine · 2026
    Review
  5. A Combined Bioinformatics and Clinical Validation Study IdentifiesInternational journal of molecular sciences · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Cracking the Endothelial Calcium (CaInternational journal of molecular sciences · 2023
    Review
  14. Article
  15. Review
  16. The Molecular Heterogeneity of Store-Operated CaInternational journal of molecular sciences · 2023
    Review
  17. Drug design, development and therapy · 2023
    Article
  18. Transient Receptor Potential (TRP) Channels in Tumor Vascularization.International journal of molecular sciences · 2022
    Review
  19. Article
  20. 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

6 authors at 3 institutions in 1 country.

Pawan FarisLaboratory of General Physiology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.ORCID 0000-0001-6867-0359
Sharon NegriLaboratory of General Physiology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.
Angelica PernaDepartment of Medicine and Health Sciences "Vincenzo Tiberio", University of Molise, 86100 Campobasso, Italy.
Vittorio RostiCenter for the Study of Myelofibrosis, Laboratory of Biochemistry, Biotechnology and Advanced Diagnosis, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Germano GuerraDepartment of Medicine and Health Sciences "Vincenzo Tiberio", University of Molise, 86100 Campobasso, Italy.ORCID 0000-0002-4342-962X
Francesco MocciaLaboratory of General Physiology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.ORCID 0000-0003-0010-0098
University of Pavia · ITUniversity of Molise · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

EU Horizon 2020 FETOPEN-2018-2020 Program Grant Agreement N. 828984Italian Ministry of Education, University and Research (MIUR) Dipartimenti di Eccellenza Program (2018-2022) - Dept. of Biology and Biotechnology "L. Spallanzani",University of Pavia Fondo Ricerca Giovani
6 · The paper itself

Abstract

Cardiovascular disease (CVD) comprises a range of major clinical cardiac and circulatory diseases, which produce immense health and economic burdens worldwide. Currently, vascular regenerative surgery represents the most employed therapeutic option to treat ischemic disorders, even though not all the patients are amenable to surgical revascularization. Therefore, more efficient therapeutic approaches are urgently required to promote neovascularization. Therapeutic angiogenesis represents an emerging strategy that aims at reconstructing the damaged vascular network by stimulating local angiogenesis and/or promoting de novo blood vessel formation according to a process known as vasculogenesis. In turn, circulating endothelial colony-forming cells (ECFCs) represent truly endothelial precursors, which display high clonogenic potential and have the documented ability to originate de novo blood vessels in vivo. Therefore, ECFCs are regarded as the most promising cellular candidate to promote therapeutic angiogenesis in patients suffering from CVD. The current briefly summarizes the available information about the origin and characterization of ECFCs and then widely illustrates the preclinical studies that assessed their regenerative efficacy in a variety of ischemic disorders, including acute myocardial infarction, peripheral artery disease, ischemic brain disease, and retinopathy. Then, we describe the most common pharmacological, genetic, and epigenetic strategies employed to enhance the vasoreparative potential of autologous ECFCs by manipulating crucial pro-angiogenic signaling pathways, e.g., extracellular-signal regulated kinase/Akt, phosphoinositide 3-kinase, and Ca

Indexed as

Cell- and Tissue-Based TherapyStem Cell TransplantationAnimalsBiomarkersCell DifferentiationChemotaxisDisease ManagementDisease SusceptibilityEndothelial Progenitor CellsGene Expression RegulationHumansIschemiaMesenchymal Stem CellsNeovascularization, PhysiologicPhenotypeSignal TransductionBiomarkerscardiovascular diseaseendothelial colony forming cellsgenetic modificationischemic disorderspharmacological conditioningsignaling pathwaystherapeutic angiogenesis

Identifiers

PMID33036489
PMCPMC7582994
OpenAlexW3087935132

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.