Evidence map›Paper›PMID 10433934›Full record

ArticleThe American journal of pathology1999

Three-dimensional reconstruction of pulmonary arteries in plexiform pulmonary hypertension using cell-specific markers. Evidence for a dynamic and heterogeneous process of pulmonary endothelial cell growth.

C D Cool, J S Stewart, P Werahera, G J Miller, R L Williams, N F Voelkel, R M Tuder

Open access · hybridAbstract read
In one paragraph

Article in The American journal of pathology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
9.4field-weighted citation impact, top 2% 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

93 citing papers in PubMed, 307 citations in OpenAlex.

  1. Article
  2. Review
  3. Sildenafil Effect on Atrial Natriuretic Peptide Level in Pulmonary Hypertensive Rats.Cardiovascular & hematological agents in medicinal chemistry · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Distinct types of plexiform lesions identified by synchrotron-based phase-contrast micro-CT.American journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  16. Review
  17. Review
  18. Article
  19. The hallmarks of severe pulmonary arterial hypertension: the cancer hypothesis-ten years later.American journal of physiology. Lung cellular and molecular physiology · 2020
    Review
  20. Perspective: pathobiological paradigms in pulmonary hypertension, time for reappraisal.American journal of physiology. Lung cellular and molecular physiology · 2020
    Review

33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

C D CoolPulmonary Hypertension Center,Departments of Pathology, University of Colorado Health Sciences Center, Denver, Colorado, USA. carlyne.cool@uchsc.edu
J S Stewart
P Werahera
G J Miller
R L Williams
N F Voelkel
R M Tuder
University of Colorado Health · US

Funding

ENDOTHELIAL CELL PROLIFERATION IN PPHR01HL060913 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI VOELKEL, NORBERT F · 1998 to 2000
$231k
NHLBI NIH HHS R01HL60913-01
6 · The paper itself

Abstract

The plexiform lesions of severe pulmonary hypertension (PH) are complex vascular structures composed primarily of endothelial cells. In this study, we use immunohistochemical markers to identify the various cell layers of pulmonary vessels and to identify different endothelial cell phenotypes in pulmonary arteries affected by severe PH. Our computerized three-dimensional reconstructions of nine vessels in five patients with severe PH demonstrate that plexiform (n = 14) and concentric-obliterative (n = 6) lesions occur distal to branch points of small pulmonary arteries. And, whereas plexiform lesions occur as solitary lesions, concentric-obliterative lesions appear to be only associated with, and proximal to, plexiform structures. The endothelial cells of plexiform lesions express intensely and uniformly the vascular endothelial growth factor (VEGF) receptor KDR and segregate phenotypically into cyclin-kinase inhibitor p27/kip1-negative cells in the central core of the plexiform lesion and p27/kip1-positive cells in peripheral areas adjacent to incipient blood vessel formation. Using immunohistochemistry and three-dimensional reconstruction techniques, we show that plexiform lesions are dynamic vascular structures characterized by at least two endothelial cell phenotypes. Plexiform arteriopathy is not merely an end stage or postthrombotic change--it may represent one stage in an ongoing, angiogenic endothelial cell growth process.

Indexed as

Cell Cycle ProteinsComputer SimulationTumor Suppressor ProteinsActinsAdultBiomarkersCell DivisionCyclin-Dependent Kinase Inhibitor p27Endothelial Growth FactorsEndotheliumFemaleHumansHypertension, PulmonaryImage Processing, Computer-AssistedImmunohistochemistryLungActinsBiomarkersCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p27Endothelial Growth FactorsLymphokinesMicrotubule-Associated ProteinsReceptor Protein-Tyrosine KinasesReceptors, Growth FactorReceptors, Vascular Endothelial Growth FactorTumor Suppressor ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factorsvon Willebrand Factor

Identifiers

PMID10433934
PMCPMC1866857
OpenAlexW1508826385

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.