Evidence map›Paper›PMID 40645813›Full record

ReviewTrends in cell biology2026

Proteoglycans are protagonists in autophagy, lymphangiogenesis, and neurodegenerative diseases.

Gabriel J Pascal, Sadie Kim, Christopher Xie, Dipon Mondal, Renato V Iozzo

Abstract readReview
In one paragraph

Review in Trends in cell biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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.

Gabriel J PascalDepartment of Pathology and Genomic Medicine, and the Translational Cellular Oncology Program, Sidney Kimmel Comprehensive Cancer Center, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA 19107, USA.
Sadie KimDepartment of Pathology and Genomic Medicine, and the Translational Cellular Oncology Program, Sidney Kimmel Comprehensive Cancer Center, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA 19107, USA.
Christopher XieDepartment of Pathology and Genomic Medicine, and the Translational Cellular Oncology Program, Sidney Kimmel Comprehensive Cancer Center, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA 19107, USA.
Dipon MondalDepartment of Pathology and Genomic Medicine, and the Translational Cellular Oncology Program, Sidney Kimmel Comprehensive Cancer Center, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA 19107, USA.
Renato V IozzoDepartment of Pathology and Genomic Medicine, and the Translational Cellular Oncology Program, Sidney Kimmel Comprehensive Cancer Center, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA 19107, USA. Electronic address: renato.iozzo@jefferson.edu.

Funding

Proteoglycan regulation of tumor angiogenesis and endothelial cell autophagyR01CA245311 · NCI · THOMAS JEFFERSON UNIVERSITY · PI IOZZO, RENATO V. · 2020 to 2024
$2.0M
Mitostatin-evoked mitophagy for breast cancer inhibitionR03CA270830 · NCI · THOMAS JEFFERSON UNIVERSITY · PI IOZZO, RENATO V. · 2023 to 2024
$156k
NCI NIH HHS R01 CA245311NCI NIH HHS R03 CA270830
6 · The paper itself

Abstract

Proteoglycans (PGs) are specialized cell-surface and secreted proteins teeming with bioactivity. They have been the subject of fascinating research on autophagy, lymphangiogenesis, and neurodegenerative diseases. PG influence on autophagy extends to several disease domains, and their ability to alter autophagic processes has highlighted their suitability as therapeutic targets. PGs also display new functions by evoking protracted autophagy in lymphatic endothelial cells and inhibiting tumor and physiological lymphangiogenesis. The variable degree of PG sulfation and their ability to regulate growth-factor activities in the central nervous system has opened doors into novel therapeutic avenues including Alzheimer's and Parkinson's diseases. This review systematically integrates these diverse qualities of PGs while highlighting future directions towards clinical application.

Indexed as

AutophagyLymphangiogenesisNeurodegenerative DiseasesProteoglycansAnimalsHumansProteoglycansautophagylymphangiogenesisneurodegenerationproteoglycantau aggregation

Identifiers

PMID40645813
PMCPMC12258961

What OpenQuestion holds

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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.