Evidence map›Paper›PMID 33249487›Full record

ArticleNeuro-oncology2021

Alpha 1-antichymotrypsin contributes to stem cell characteristics and enhances tumorigenicity of glioblastoma.

Montserrat Lara-Velazquez, Natanael Zarco, Anna Carrano, Jordan Phillipps, Emily S Norton, Paula Schiapparelli, Rawan Al-Kharboosh, Jordina Rincon-Torroella, Stephanie Jeanneret, Teresa Corona and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuro-oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.0field-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

30 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  4. The glymphatic system and glioblastoma.Brain : a journal of neurology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 2 countries.

Montserrat Lara-VelazquezPECEM, UNAM, Mexico City, Mexico.
Natanael ZarcoDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA.
Anna CarranoPECEM, UNAM, Mexico City, Mexico.
Jordan PhillippsPECEM, UNAM, Mexico City, Mexico.
Emily S NortonPECEM, UNAM, Mexico City, Mexico.
Paula SchiapparelliPECEM, UNAM, Mexico City, Mexico.
Rawan Al-KharbooshPECEM, UNAM, Mexico City, Mexico.
Jordina Rincon-TorroellaDepartment of Neurosurgery, Johns Hopkins Hospital, Baltimore, MD, USA.
Stephanie JeanneretPECEM, UNAM, Mexico City, Mexico.
Teresa CoronaClinical Laboratory of Neurodegenerative Diseases, National Institute of Neurology and Neurosurgery, Mexico City, Mexico.
Jose SegoviaDepartment of Physiology, Biophysics and Neurosciences, Cinvestav-IPN, Mexico City, Mexico.
Mark E JentoftDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, Florida, USA.
Kaisorn L ChaichanaPECEM, UNAM, Mexico City, Mexico.
Yan W AsmannDepartment of Health Sciences Research, Mayo Clinic, Jacksonville, Florida, USA.
Alfredo Quiñones-HinojosaPECEM, UNAM, Mexico City, Mexico.
Hugo Guerrero-CazaresPECEM, UNAM, Mexico City, Mexico.
Jacksonville College · USMayo Clinic · USInstituto Nacional de Neurología y Neurocirugía · MXInstituto Politécnico Nacional · MXJohns Hopkins Hospital · USMayo Clinic in Florida · US

Funding

Intra-Operative, Label-Free Detection of Brain Cancer Infiltration with Quantitative Optical ImagingR01CA200399 · NCI · JOHNS HOPKINS UNIVERSITY · PI LI, XINGDE, QUINONES-HINOJOSA, ALFREDO · 2016 to 2020
$3.0M
A novel microfluidic device to predict brain cancer prognosis and response to therapyR01CA216855 · NCI · MAYO CLINIC JACKSONVILLE · PI KONSTANTOPOULOS, KONSTANTINOS, QUINONES-HINOJOSA, ALFREDO · 2018 to 2022
$2.4M
Nanoparticle Modified Human Fat Derived Mesenchymal Stem Cells for Brain Cancer (Change of Organization Application)R01CA195503 · NCI · MAYO CLINIC JACKSONVILLE · PI GREEN, JORDAN, QUINONES-HINOJOSA, ALFREDO · 2016 to 2020
$1.9M
BMP4 Engineered Mesenchymal Stem Cell Therapy for GlioblastomaR01CA183827 · NCI · MAYO CLINIC JACKSONVILLE · PI QUINONES-HINOJOSA, ALFREDO · 2015 to 2019
$1.9M
Osteopontin-CD44 role in the malignancy of lateral ventricle infiltrating glioblastomaK01NS110930 · NINDS · MAYO CLINIC JACKSONVILLE · PI GUERRERO-CAZARES, HUGO · 2019 to 2023
$1.1M
Chemically produced neural progenitors as a delivery vehicle for anti-glioma therapyR43CA221490 · NCI · CELL REPROGRAMMING AND THERAPEUTICS, LLC · PI ALEXANIAN, ARSHAK R, QUINONES-HINOJOSA, ALFREDO · 2018 to 2018
$300k
Role of SerpinA3 in the response of glioblastoma to cerebrospinal fluidR03NS109444 · NINDS · MAYO CLINIC JACKSONVILLE · PI GUERRERO-CAZARES, HUGO · 2018 to 2019
$236k
NCI NIH HHS R01 CA183827NCI NIH HHS R01 CA195503NCI NIH HHS R01 CA200399NCI NIH HHS R01 CA216855NCI NIH HHS R43 CA221490NINDS NIH HHS K01 NS110930NINDS NIH HHS R03 NS109444
6 · The paper itself

Abstract

backgroundGlioblastomas (GBMs) are the main primary brain tumors in adults with almost 100% recurrence rate. Patients with lateral ventricle proximal GBMs (LV-GBMs) exhibit worse survival compared to distal locations for unknown reasons. One hypothesis is the proximity of these tumors to the cerebrospinal fluid (CSF) and its chemical cues that can regulate cellular phenotype. We therefore investigated the role of CSF on GBM gene expression and the role of a CSF-induced gene, SERPINA3, in GBM malignancy in vitro and in vivo.

methodsWe utilized human CSF and GBM brain tumor-initiating cells (BTICs). We determined the impact of SERPINA3 expression in glioma patients using The Cancer Genome Atlas (TCGA) database. SERPINA3 expression changes were evaluated at mRNA and protein levels. The effects of knockdown (KD) and overexpression (OE) of SERPINA3 on cell migration, viability and cell proliferation were evaluated. Stem cell characteristics on KD cells were evaluated by differentiation and colony formation experiments. Tumor growth was studied by intracranial and flank injections.

resultsGBM-CSF increased BTIC migration accompanied by upregulation of the SERPINA3 gene. In patient samples and TCGA data, we observed SERPINA3 to correlate directly with brain tumor grade and indirectly with GBM patient survival. SERPINA3 KD induced a decrease in cell proliferation, migration, invasion, and stem cell characteristics, while SERPINA3 OE increased cell migration. In vivo, SERPINA3 KD BTICs showed increased survival in a murine model.

conclusionsSERPINA3 plays a key role in GBM malignancy and its inhibition results in a better outcome using GBM preclinical models.

Indexed as

alpha 1-AntichymotrypsinBrain NeoplasmsGlioblastomaNeoplastic Stem CellsAdultAnimalsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansMiceSerpinsalpha 1-AntichymotrypsinSERPINA3 protein, humanSerpinsalpha 1-antichymotrypsinbrain tumorcerebrospinal fluidglioblastomaSERPINA3

Identifiers

PMID33249487
PMCPMC8041345
OpenAlexW3106727171

What OpenQuestion holds

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Registered trials

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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.