Evidence map›Paper›PMID 40400414›Full record

ReviewMicrocirculation (New York, N.Y. : 1994)2025

Clinical Relevance of Animal Models of Lymphatic Dysfunction and Lymphedema.

Pritam Saha Podder, Debasree Bhadra, Soumiya Pal, V Suzanne Klimberg, Amanda J Stolarz

Abstract readReview
In one paragraph

Review in Microcirculation (New York, N.Y. : 1994), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. A Novel Lymphosome-Based Long-Lasting Rat Tail Model of Lymphedema.Journal of reconstructive microsurgery · 2026
    Article
  3. Article
  4. 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

5 authors.

Pritam Saha PodderDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Debasree BhadraDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Soumiya PalDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.ORCID 0000-0002-8003-9866
V Suzanne KlimbergDivision of Surgical Oncology, Department of Surgery, University of Texas Medical Branch, Galveston, Texas, USA.
Amanda J StolarzDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.ORCID 0000-0002-7082-8239

Funding

Ryanodine Receptors as Therapeutic Targets to Prevent Doxorubicin-Induced Lymphatic DysfunctionR37CA282349 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI Amanda Stolarz · 2023 to 2026
$1.4M
American Heart Association 23PRE1020738National Institutes of Health (NIH) through the National Cancer Institute (NCI) R37-CA282349NCI NIH HHS R37 CA282349
6 · The paper itself

Abstract

Lymphedema is a chronic progressive condition, and treatment options are limited to physical therapy or surgical intervention, underscoring the need to develop preventative strategies. To do so, we must first understand the underlying mechanisms that contribute to the development of clinical lymphedema, which can be caused by a myriad of factors, including genetic mutations, infectious agents, and cancer treatments. Animal models are essential to study the pathogenesis of clinical lymphedema and to develop therapeutic interventions. Many animal models mimic the various aspects of lymphatic dysfunction and lymphedema seen in humans, and some species better represent different aspects or causes of lymphedema. However, no single model perfectly recapitulates human disease in a cost- and time-efficient manner; therefore, findings should be verified in multiple models and multiple species. In doing so, researchers will increase the likelihood of collecting rigorous, reliable data that could be effectively and efficiently translated into the clinic. This review explores genetic, infectious, and surgical animal models of lymphatic dysfunction and lymphedema and describes how these models can be used to understand clinical forms of lymphedema. Collectively, this information can provide valuable insight for the translational study of lymphatic diseases.

Indexed as

Disease Models, AnimalLymphedemaAnimalsClinical RelevanceHumansanimal modelsbreast cancer related lymphedemafilariasislymphatic dysfunctionlymphedemasurgical models

Identifiers

PMID40400414
PMCPMC12096149

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.