Evidence map›Paper›PMID 34572134›Full record

ArticleCells2021

The Presence and Potential Role of ALDH1A2 in the Glioblastoma Microenvironment.

Stephanie Sanders, Denise M Herpai, Analiz Rodriguez, Yue Huang, Jeff Chou, Fang-Chi Hsu, Darren Seals, Ryan Mott, Lance D Miller, Waldemar Debinski

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Stephanie SandersDepartment of Cancer Biology, Wake Forest School of Medicine, Winston Salem, NC 27157, USA.
Denise M HerpaiDepartment of Cancer Biology, Wake Forest School of Medicine, Winston Salem, NC 27157, USA.
Analiz RodriguezDepartment of Neurosurgery, Jackson T. Stephens Spine and Neuroscience Institute, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.ORCID 0000-0003-3426-0508
Yue HuangDepartment of Cancer Biology, Wake Forest School of Medicine, Winston Salem, NC 27157, USA.
Jeff ChouDepartment of Cancer Biology, Wake Forest School of Medicine, Winston Salem, NC 27157, USA.
Fang-Chi HsuDepartment of Biostatistics and Data Science, Wake Forest School of Medicine, Winston Salem, NC 27157, USA.
Darren SealsBiology Department, Appalachian State University, Boone, NC 28608, USA.ORCID 0000-0001-9163-7338
Ryan MottDepartment of Pathology, Wake Forest School of Medicine, Winston Salem, NC 27157, USA.
Lance D MillerDepartment of Cancer Biology, Wake Forest School of Medicine, Winston Salem, NC 27157, USA.
Waldemar DebinskiDepartment of Cancer Biology, Wake Forest School of Medicine, Winston Salem, NC 27157, USA.
Atrium Health Wake Forest Baptist · USWake Forest University · USAppalachian State University · USWinthrop Rockefeller Foundation · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
TUMOR SPECIFIC TARGET FOR THERAPEUTIC DELIVERIESR01CA074145 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DEBINSKI, WALDEMAR · 1998 to 2019
$4.9M
NCI NIH HHS P30 CA012197NCI NIH HHS RO1 CA074145
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most aggressive malignant glioma. Therapeutic targeting of GBM is made more difficult due to its heterogeneity, resistance to treatment, and diffuse infiltration into the brain parenchyma. Better understanding of the tumor microenvironment should aid in finding more effective management of GBM. GBM-associated macrophages (GAM) comprise up to 30% of the GBM microenvironment. Therefore, exploration of GAM activity/function and their specific markers are important for developing new therapeutic agents. In this study, we identified and evaluated the expression of ALDH1A2 in the GBM microenvironment, and especially in M2 GAM, though it is also expressed in reactive astrocytes and multinucleated tumor cells. We demonstrated that M2 GAM highly express ALDH1A2 when compared to other ALDH1 family proteins. Additionally, GBM samples showed higher expression of ALDH1A2 when compared to low-grade gliomas (LGG), and this expression was increased upon tumor recurrence both at the gene and protein levels. We demonstrated that the enzymatic product of ALDH1A2, retinoic acid (RA), modulated the expression and activity of MMP-2 and MMP-9 in macrophages, but not in GBM tumor cells. Thus, the expression of ALDH1A2 may promote the progressive phenotype of GBM.

Indexed as

Gene Expression Regulation, NeoplasticAldehyde Dehydrogenase 1 FamilyApoptosisBrain NeoplasmsCell MovementCell ProliferationGlioblastomaHumansMacrophagesMatrix Metalloproteinase 2Matrix Metalloproteinase 9Retinal DehydrogenaseTretinoinTumor Cells, CulturedTumor MicroenvironmentAldehyde Dehydrogenase 1 FamilyALDH1A2 protein, humanMatrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humanRetinal DehydrogenaseTretinoinALDH1A2enzymeglioblastomainvasionlow-grade gliomamacrophagesMMPmonocytic cellsprogressionretinoic acidsingle-cell sequencingtumor-associated macrophagestumor microenvironment

Identifiers

PMID34572134
PMCPMC8468822
OpenAlexW3199766594

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.