Evidence map›Paper›PMID 33200983›Full record

ArticleeLife2020

Lymphangiogenic therapy prevents cardiac dysfunction by ameliorating inflammation and hypertension.

LouJin Song, Xian Chen, Terri A Swanson, Brianna LaViolette, Jincheng Pang, Teresa Cunio, Michael W Nagle, Shoh Asano, Katherine Hales, Arun Shipstone and 11 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Normal cardiac lymphatics and their mimics.American journal of physiology. Heart and circulatory physiology · 2026
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Hypertension: a lymphatic disease?Clinical science (London, England : 1979) · 2025
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Angiogenesis-An Emerging Role in Organ Fibrosis.International journal of molecular sciences · 2023
    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

21 authors at 3 institutions in 1 country.

LouJin SongInternal Medicine Research Unit, Pfizer Inc, Cambridge, United States.ORCID 0000-0002-1646-8121
Xian ChenComparative Medicine, Pfizer Inc, Cambridge, United States.
Terri A SwansonEarly Clinical Development, Pfizer Inc, Cambridge, United States.
Brianna LaVioletteComparative Medicine, Pfizer Inc, Cambridge, United States.
Jincheng PangInternal Medicine Research Unit, Pfizer Inc, Cambridge, United States.
Teresa CunioInternal Medicine Research Unit, Pfizer Inc, Cambridge, United States.
Michael W NagleInternal Medicine Research Unit, Pfizer Inc, Cambridge, United States.
Shoh AsanoInternal Medicine Research Unit, Pfizer Inc, Cambridge, United States.
Katherine HalesInternal Medicine Research Unit, Pfizer Inc, Cambridge, United States.
Arun ShipstoneInflammation and Immunology Research Unit, Pfizer Inc, Cambridge, United States.
Hanna SobonInflammation and Immunology Research Unit, Pfizer Inc, Cambridge, United States.
Sabra D Al-HarthyComparative Medicine, Pfizer Inc, Cambridge, United States.
Youngwook AhnTarget Sciences, Emerging Science and Innovation, Pfizer Inc, Cambridge, United States.
Steven KreuserComparative Medicine, Pfizer Inc, Cambridge, United States.
Andrew RobertsonDrug Safety Research & Development, Pfizer Inc, Groton, United States.
Casey RitenourDrug Safety Research & Development, Pfizer Inc, Groton, United States.
Frank VoigtDrug Safety Research & Development, Pfizer Inc, Groton, United States.
Magalie BoucherDrug Safety Research & Development, Pfizer Inc, Groton, United States.
Furong SunEarly Clinical Development, Pfizer Inc, Cambridge, United States.
William C SessaDepartment of Pharmacology, Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, United States.ORCID 0000-0001-5759-1938
Rachel J Roth FlachInternal Medicine Research Unit, Pfizer Inc, Cambridge, United States.ORCID 0000-0003-2754-828X
Pfizer (United States) · USTarget (United States) · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lymphatic vasculature is involved in the pathogenesis of acute cardiac injuries, but little is known about its role in chronic cardiac dysfunction. Here, we demonstrate that angiotensin II infusion induced cardiac inflammation and fibrosis at 1 week and caused cardiac dysfunction and impaired lymphatic transport at 6 weeks in mice, while co-administration of VEGFCc156s improved these parameters. To identify novel mechanisms underlying this protection, RNA sequencing analysis in distinct cell populations revealed that VEGFCc156s specifically modulated angiotensin II-induced inflammatory responses in cardiac and peripheral lymphatic endothelial cells. Furthermore, telemetry studies showed that while angiotensin II increased blood pressure acutely in all animals, VEGFCc156s-treated animals displayed a delayed systemic reduction in blood pressure independent of alterations in angiotensin II-mediated aortic stiffness. Overall, these results demonstrate that VEGFCc156s had a multifaceted therapeutic effect to prevent angiotensin II-induced cardiac dysfunction by improving cardiac lymphatic function, alleviating fibrosis and inflammation, and ameliorating hypertension.

Indexed as

Angiotensin IIAnimalsBiomarkersEndothelial CellsGene Knock-In TechniquesGenome-Wide Association StudyGreen Fluorescent ProteinsHeart DiseasesHomeodomain ProteinsHumansHypertensionMaleMiceMice, Inbred C57BLMyocardiumProspero-Related Homeobox 1 ProteinAngiotensin IIBiomarkersenhanced green fluorescent proteinGreen Fluorescent ProteinsHomeodomain ProteinsProspero-Related Homeobox 1 ProteinTumor Suppressor ProteinsVascular Endothelial Growth Factor Ccardiac dysfunctioncell biologyendothelialfibrosishumanhypertensioninflammationlymphaticmedicinemouse

Identifiers

PMID33200983
PMCPMC7695461
OpenAlexW3103900504

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.