Evidence map›Paper›PMID 39120311›Full record

ArticleCells2024

Discovery of Cell Number-Interstitial Fluid Volume (CIF) Ratio Reveals Secretory Autophagy Pathway to Supply eHsp90α for Wound Healing.

Cheng Chang, Xin Tang, Axel H Schönthal, Mei Chen, David T Woodley, Yanzhuang Wang, Chengyu Liang, Wei Li

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Cheng ChangDepartment of Dermatology and the USC-Norris Comprehensive Cancer Centre, Los Angeles, CA 90089, USA.
Xin TangDepartment of Dermatology and the USC-Norris Comprehensive Cancer Centre, Los Angeles, CA 90089, USA.ORCID 0000-0002-5043-5972
Axel H SchönthalDepartment of Molecular Microbiology & Immunology, University of Southern California Keck Medical Centre, Los Angeles, CA 90033, USA.ORCID 0000-0003-0662-5653
Mei ChenDepartment of Dermatology and the USC-Norris Comprehensive Cancer Centre, Los Angeles, CA 90089, USA.
David T WoodleyDepartment of Dermatology and the USC-Norris Comprehensive Cancer Centre, Los Angeles, CA 90089, USA.
Yanzhuang WangDepartment of Molecular, Cellular and Developmental Biology, University of Michigan, 1105 North University Avenue, Ann Arbor, MI 48109, USA.ORCID 0000-0002-1864-7094
Chengyu LiangMolecular and Cellular Oncogenesis Program, The Wistar Institute, 3601 Spruce Street, Philadelphia, PA 19104, USA.ORCID 0000-0001-6082-2143
Wei LiDepartment of Dermatology and the USC-Norris Comprehensive Cancer Centre, Los Angeles, CA 90089, USA.ORCID 0000-0001-9230-5327

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Role of UVRAG-mediated Autophagy in Tumor SuppressionR01CA140964 · NCI · WISTAR INSTITUTE · PI LIANG, CHENGYU · 2009 to 2025
$5.4M
Mechanisms of Human Dermal Fibroblast MigrationR01GM067100 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LI, WEI · 2003 to 2020
$5.2M
Transcriptional Reprogramming in Melanoma PlasticityR01CA289624 · NCI · WISTAR INSTITUTE · PI Chengyu Liang · 2024 to 2026
$3.0M
Molecular Mechanism of UV Protection in Cutaneous MelanomaR01ES029092 · NIEHS · WISTAR INSTITUTE · PI LIANG, CHENGYU · 2019 to 2023
$3.0M
A cancer-derived truncating mutation in disease penetrance and progression of MSI CRCR01CA238457 · NCI · WISTAR INSTITUTE · PI LIANG, CHENGYU · 2020 to 2024
$2.9M
New control of oncogene activation in T-cell leukemiaR01CA262631 · NCI · WISTAR INSTITUTE · PI Chengyu Liang · 2022 to 2026
$2.6M
NCI NIH HHS P30 CA010815NCI NIH HHS R01 CA140964NCI NIH HHS R01 CA238457NCI NIH HHS R01 CA262631NCI NIH HHS R01 CA289624NIEHS NIH HHS R01 ES029092NIGMS NIH HHS R01 GM067100NIH HHS GM067100 and W81XWH-1810558
6 · The paper itself

Abstract

Cell secretion repairs tissue damage and restores homeostasis throughout adult life. The extracellular heat shock protein-90alpha (eHsp90α) has been reported as an exosome cargo and a potential driver of wound healing. However, neither the mechanism of secretion nor the genetic evidence for eHsp90α in wound healing has been substantiated. Herein, we show that tissue injury causes massive deposition of eHsp90α in tissues and secretion of eHsp90α by cells. Sequential centrifugations of conditioned medium from relevant cell lines revealed the relative distributions of eHsp90α in microvesicle, exosome and trypsin-sensitive supernatant fractions to be approximately <2%, <4% and >95%, respectively. Establishing the cell-number-to-interstitial-fluid-volume (CIF) ratio for the microenvironment of human tissues as 1 × 10

Indexed as

AutophagyExtracellular FluidHSP90 Heat-Shock ProteinsWound HealingAnimalsCell LineExosomesHumansMaleMiceSecretory PathwayHSP90AA2P protein, humanHSP90 Heat-Shock Proteinsbiomarkersconditioned mediumHsp90interstitial fluidtissue microenvironmentwound healing

Identifiers

PMID39120311
PMCPMC11312289

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.