Evidence map›Paper›PMID 36231065›Full record

ArticleCells2022

Exosomal Plasminogen Activator Inhibitor-1 Induces Ionizing Radiation-Adaptive Glioblastoma Cachexia.

Eunguk Shin, Hyunkoo Kang, Haksoo Lee, Sungmin Lee, Jaewan Jeon, Kimoon Seong, Hyesook Youn, Buhyun Youn

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  11. The role of extracellular vesicles in skeletal muscle wasting.Journal of cachexia, sarcopenia and muscle · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Eunguk ShinDepartment of Integrated Biological Science, Pusan National University, Busan 46241, Korea.
Hyunkoo KangDepartment of Integrated Biological Science, Pusan National University, Busan 46241, Korea.
Haksoo LeeDepartment of Integrated Biological Science, Pusan National University, Busan 46241, Korea.
Sungmin LeeDepartment of Integrated Biological Science, Pusan National University, Busan 46241, Korea.
Jaewan JeonDepartment of Radiation Oncology, Haeundae Paik Hospital, Inje University College of Medicine, Busan 48108, Korea.
Kimoon SeongLaboratory of Biological Dosimetry, National Radiation Emergency Medical Center (NREMC), Korea Institute of Radiological and Medical Sciences (KIRAMS), Seoul 01812, Korea.ORCID 0000-0003-3530-5587
Hyesook YounDepartment of Integrative Bioscience and Biotechnology, Sejong University, Seoul 05006, Korea.ORCID 0000-0003-0919-094X
Buhyun YounDepartment of Integrated Biological Science, Pusan National University, Busan 46241, Korea.
Pusan National University · KRInje University Haeundae Paik Hospital · KRKorea Institute of Radiological and Medical Sciences · KRSejong University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cachexia is a muscle-wasting syndrome that leads to a severely compromised quality of life and increased mortality. A strong association between cachexia and poor prognosis has been demonstrated in intractable cancers, including glioblastoma (GBM). In the present study, it was demonstrated that ionizing radiation (IR), the first-line treatment for GBM, causes cancer cachexia by increasing the exosomal release of plasminogen activator inhibitor-1 (PAI-1) from glioblastoma cells. Exosomal PAI-1 delivered to the skeletal muscle is directly penetrated in the muscles and phosphorylates STAT3 to intensify muscle atrophy by activating muscle RING-finger protein-1 (MuRF1) and muscle atrophy F-box (Atrogin1); furthermore, it hampers muscle protein synthesis by inhibiting mTOR signaling. Additionally, pharmacological inhibition of PAI-1 by TM5441 inhibited muscle atrophy and rescued muscle protein synthesis, thereby providing survival benefits in a GBM orthotopic xenograft mouse model. In summary, our data delineated the role of PAI-1 in the induction of GBM cachexia associated with radiotherapy-treated GBM. Our data also indicated that targeting PAI-1 could serve as an attractive strategy for the management of GBM following radiotherapy, which would lead to a considerable improvement in the quality of life of GBM patients undergoing radiotherapy.

Indexed as

CachexiaGlioblastomaAnimalsHumansMiceMuscle ProteinsMuscular AtrophyPlasminogen Activator Inhibitor 1Quality of LifeRadiation, IonizingTOR Serine-Threonine KinasesMuscle ProteinsPlasminogen Activator Inhibitor 1TOR Serine-Threonine KinasescachexiaexosomeglioblastomaPAI-1radiotherapy

Identifiers

PMID36231065
PMCPMC9564109
OpenAlexW4303628190

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.