Evidence map›Paper›PMID 42273731›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2026

Phosphoproteomics in Vascular Biology and Disease: Illuminating Signaling in the Vessel.

Kayleigh Voos, Ming He, Gina M Many, Yabing Chen, Wei-Jun Qian

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kayleigh VoosBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA (K.V., G.M.M., W.-J.Q.).ORCID 0000-0002-2857-9515
Ming HeDepartment of Pathology, The University of Alabama at Birmingham (M.H.).ORCID 0000-0001-8867-1826
Gina M ManyBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA (K.V., G.M.M., W.-J.Q.).ORCID 0000-0003-4779-1690
Yabing ChenDepartment of Pathology and Laboratory Medicine, Oregon Health and Science University, Portland (Y.C.).ORCID 0000-0001-9676-6657
Wei-Jun QianBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA (K.V., G.M.M., W.-J.Q.).ORCID 0000-0002-5393-2827

Funding

Discovery and Roles of In Situ Islet Neoantigens in Human Type 1 DiabetesR01DK135081 · NIDDK · UNIVERSITY OF FLORIDA · PI CLAYTON E MATHEWS, DAVID A OSTROV · 2023 to 2026
$2.8M
Histone H3 O-GlcNAcylation in Endothelial Cells Promotes Diabetic Vascular ComplicationsR01DK144096 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HE, MING · 2025 to 2025
$2.4M
Unveiling the Atheroprone Role of Novel Mechanosensitive Histone ModificationR01HL178662 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Ming He · 2025 to 2026
$1.1M
8OH-G miR-483 contributes to the aging-accelerated atherosclerosisR21AG075450 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HE, MING · 2022 to 2023
$423k
NHLBI NIH HHS R01 HL178662NIA NIH HHS R21 AG075450NIDDK NIH HHS R01 DK135081NIDDK NIH HHS R01 DK144096
6 · The paper itself

Abstract

Phosphoregulatory events underlie vascular responses to environmental and pathological stimuli, regulate hemostasis and thrombosis, and drive vascular remodeling in health and disease. Consequently, defining phosphorylation-dependent signaling networks in vascular physiology and pathology has enabled biomarker discovery and informed therapeutic interventions. Advances in mass spectrometry-based phosphoproteomics have enabled accurate and high-resolution mapping of dynamic phosphorylation events at the systems level, providing comprehensive mechanistic insights into vascular signaling and pathology. In this review, we contextualize phosphorylation in the vascular niche and summarize the current state of phosphoproteomics in vascular research, highlighting experimental design considerations, technological advances, quantification strategies, and data analysis approaches to uncover biological insights from large-scale phosphoproteomic data sets. Finally, we discuss recent discoveries in vascular signaling and disease, along with current challenges and emerging directions for applying phosphoproteomics to critical questions in vascular biology.

Indexed as

Blood VesselsPhosphoproteinsProteomicsSignal TransductionVascular DiseasesAnimalsHumansPhosphorylationSystems BiologyVascular HealthVascular RemodelingPhosphoproteinsphosphorylationproteomicssignal transductionsystems biologyvascular diseasevascular health

Identifiers

PMID42273731
PMCPMC13297492

What Socratic holds

Textmetadata
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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 Socratic graph.