Evidence map›Paper›PMID 35131870›Full record

ArticleCancer research2022

Chaperone-Mediated Autophagy Controls Proteomic and Transcriptomic Pathways to Maintain Glioma Stem Cell Activity.

Jaione Auzmendi-Iriarte, Maddalen Otaegi-Ugartemendia, Estefania Carrasco-Garcia, Mikel Azkargorta, Antonio Diaz, Ander Saenz-Antoñanzas, Joaquin Andrés Andermatten, Mikel Garcia-Puga, Idoia Garcia, Alejandro Elua-Pinin and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  3. Autophagy modulation in cancer.Nature reviews. Drug discovery · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Jaione Auzmendi-IriarteCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.
Maddalen Otaegi-UgartemendiaCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.
Estefania Carrasco-GarciaCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.
Mikel AzkargortaProteomics Platform, CIC bioGUNE, Basque Research and Technology Alliance (BRTA), CIBERehd, ProteoRed-ISCIII, Spain.
Antonio DiazDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, New York.
Ander Saenz-AntoñanzasCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.
Joaquin Andrés AndermattenDonostia University Hospital, Osakidetza, San Sebastian, Spain.ORCID 0000-0002-6402-519X
Mikel Garcia-PugaCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.ORCID 0000-0002-2975-934X
Idoia GarciaCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.
Alejandro Elua-PininDonostia University Hospital, Osakidetza, San Sebastian, Spain.
Irune RuizCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.
Nicolas SampronCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.
Felix ElortzaProteomics Platform, CIC bioGUNE, Basque Research and Technology Alliance (BRTA), CIBERehd, ProteoRed-ISCIII, Spain.ORCID 0000-0001-8839-5438
Ana Maria CuervoDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, New York.
Ander MatheuCellular Oncology Group, Biodonostia Health Research Institute, San Sebastian, Spain.
Biogipuzkoa Health Research Institute · ESAlbert Einstein College of Medicine · USCIC bioGUNE · ESIkerbasque · ES

Funding

Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VIJG, JAN · 2010 to 2024
$10.8M
Decreased Protein Degradation in AgingR37AG021904 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CUERVO, ANA MARIA · 2013 to 2022
$4.4M
NIA NIH HHS P30 AG038072NIA NIH HHS R37 AG021904
6 · The paper itself

Abstract

Chaperone-mediated autophagy (CMA) is a homeostatic process essential for the lysosomal degradation of a selected subset of the proteome. CMA activity directly depends on the levels of LAMP2A, a critical receptor for CMA substrate proteins at the lysosomal membrane. In glioblastoma (GBM), the most common and aggressive brain cancer in adulthood, high levels of LAMP2A in the tumor and tumor-associated pericytes have been linked to temozolomide resistance and tumor progression. However, the role of LAMP2A, and hence CMA, in any cancer stem cell type or in glioblastoma stem cells (GSC) remains unknown. In this work, we show that LAMP2A expression is enriched in patient-derived GSCs, and its depletion diminishes GSC-mediated tumorigenic activities. Conversely, overexpression of LAMP2A facilitates the acquisition of GSC properties. Proteomic and transcriptomic analysis of LAMP2A-depleted GSCs revealed reduced extracellular matrix interaction effectors in both analyses. Moreover, pathways related to mitochondrial metabolism and the immune system were differentially deregulated at the proteome level. Furthermore, clinical samples of GBM tissue presented overexpression of LAMP2, which correlated with advanced glioma grade and poor overall survival. In conclusion, we identified a novel role of CMA in directly regulating GSCs activity via multiple pathways at the proteome and transcriptome levels. SIGNIFICANCE: A receptor of chaperone-mediated autophagy regulates glioblastoma stem cells and may serve as a potential biomarker for advanced tumor grade and poor survival in this disease.

Indexed as

Chaperone-Mediated AutophagyGliomaAdultAutophagyHumansLysosomal-Associated Membrane Protein 2Neoplastic Stem CellsProteomicsTranscriptomeLysosomal-Associated Membrane Protein 2

Identifiers

PMID35131870
PMCPMC9359743
OpenAlexW4210888178

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.