Evidence map›Paper›PMID 28408396›Full record

ReviewJournal of leukocyte biology2017

Novel role of immature myeloid cells in formation of new lymphatic vessels associated with inflammation and tumors.

Sophia Ran, Andrew Wilber

Abstract readReview
In one paragraph

Review in Journal of leukocyte biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Ontogenesis of the Mouse Ocular Surface Lymphatic Vascular Network.Investigative ophthalmology & visual science · 2023
    Article
  8. Review
  9. CD34 positive cells as endothelial progenitor cells in biology and medicine.Frontiers in cell and developmental biology · 2023
    Review
  10. Article
  11. Article
  12. The ambivalent nature of the relationship between lymphatics and cancer.Frontiers in cell and developmental biology · 2022
    Review
  13. Lymphatic Endothelial Cell Progenitors in the Tumor Microenvironment.Advances in experimental medicine and biology · 2020
    Review
  14. Article
  15. Article
  16. Review
  17. 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

2 authors.

Sophia RanDepartment of Medical Microbiology, Immunology, and Cell Biology, Southern Illinois University School of Medicine, and Simmons Cancer Institute, Springfield, Illinois, USA sran@siumed.edu.
Andrew WilberDepartment of Medical Microbiology, Immunology, and Cell Biology, Southern Illinois University School of Medicine, and Simmons Cancer Institute, Springfield, Illinois, USA.

Funding

Novel role of myeloid-derived lymphatic progenitors in induction of breast cancer lymphaticsR01CA199649 · NCI · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI RAN, SOPHIA · 2016 to 2020
$1.7M
NF-kB mediated induction of VEGFR-3 and new lymphatic vessels in breast cancerR01CA140732 · NCI · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI RAN, SOPHIA · 2010 to 2014
$1.5M
Renal Cell Tumor-Mediated Trans-differentiation of Natural Killer CellsR15CA173657 · NCI · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI WILBER, ANDREW CHRISTROPHER · 2013 to 2013
$375k
NCI NIH HHS R01 CA140732NCI NIH HHS R01 CA199649NCI NIH HHS R15 CA173657
6 · The paper itself

Abstract

Inflammation triggers an immune cell-driven program committed to restoring homeostasis to injured tissue. Central to this process is vasculature restoration, which includes both blood and lymphatic networks. Generation of new vessels or remodeling of existing vessels are also important steps in metastasis-the major cause of death for cancer patients. Although roles of the lymphatic system in regulation of inflammation and cancer metastasis are firmly established, the mechanisms underlying the formation of new lymphatic vessels remain a subject of debate. Until recently, generation of new lymphatics in adults was thought to occur exclusively through sprouting of existing vessels without help from recruited progenitors. However, emerging findings from clinical and experimental studies show that lymphoendothelial progenitors, particularly those derived from immature myeloid cells, play an important role in this process. This review summarizes current evidence for the existence and significant roles of myeloid-derived lymphatic endothelial cell progenitors (M-LECPs) in generation of new lymphatics. We describe specific markers of M-LECPs and discuss their biologic behavior in culture and in vivo, as well as currently known molecular mechanisms of myeloid-lymphatic transition (MLT). We also discuss the implications of M-LECPs for promoting adaptive immunity, as well as cancer metastasis. We conclude that improved mechanistic understanding of M-LECP differentiation and its role in adult lymphangiogenesis may lead to new therapeutic approaches for correcting lymphatic insufficiency or excessive formation of lymphatic vessels in human disorders.

Indexed as

AnimalsCell DifferentiationEndothelial CellsHumansInflammationLymphangiogenesisLymphatic VesselsMyeloid CellsNeoplasmsNeovascularization, PathologicStem Cellsendothelial progenitorsinflammatory/tumor lymphangiogenesislineage development

Identifiers

PMID28408396
PMCPMC5505745

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.