Evidence map›Paper›PMID 35008989›Full record

ArticleInternational journal of molecular sciences2022

Loss of SDHB Induces a Metabolic Switch in the hPheo1 Cell Line toward Enhanced OXPHOS.

Mouna Tabebi, Ravi Kumar Dutta, Camilla Skoglund, Peter Söderkvist, Oliver Gimm

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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  14. Frontiers in genetics · 2022
    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

5 authors.

Mouna TabebiDepartment of Biomedical and Clinical Sciences (BKV), Linköping University, 581 83 Linköping, Sweden.ORCID 0000-0002-2873-161X
Ravi Kumar DuttaDepartment of Biomedical and Clinical Sciences (BKV), Linköping University, 581 83 Linköping, Sweden.
Camilla SkoglundDepartment of Biomedical and Clinical Sciences (BKV), Linköping University, 581 83 Linköping, Sweden.
Peter SöderkvistDepartment of Biomedical and Clinical Sciences (BKV), Linköping University, 581 83 Linköping, Sweden.
Oliver GimmDepartment of Surgery and Department of Biomedical and Clinical Sciences (BKV), Linköping University, 581 83 Linköping, Sweden.ORCID 0000-0002-0054-664X

Funding

ALF Grant from Region Östergötland RÖ-607911Lisa och Johan Grönbergs Foundation 2019-00175LiU Cancer LiU2017LiU Cancer LiU-2019
6 · The paper itself

Abstract

backgroundEnzymes of tricarboxylic acid (TCA) have recently been recognized as tumor suppressors. Mutations in the SDHB subunit of succinate dehydrogenase (SDH) cause pheochromocytomas and paragangliomas (PCCs/PGLs) and predispose patients to malignant disease with poor prognosis.

methodsUsing the human pheochromocytoma cell line (hPheo1), we knocked down SDHB gene expression using CRISPR-cas9 technology.

resultsMicroarray gene expression analysis showed that >500 differentially expressed gene targets, about 54%, were upregulated in response to SDHB knock down. Notably, genes involved in glycolysis, hypoxia, cell proliferation, and cell differentiation were up regulated, whereas genes involved in oxidative phosphorylation (OXPHOS) were downregulated. In vitro studies show that hPheo1 proliferation is not affected negatively and the cells that survive by shifting their metabolism to the use of glutamine as an alternative energy source and promote OXPHOS activity. Knock down of SDHB expression results in a significant increase in

conclusionsOur data suggest that the downregulation of SDHB in PCCs/PGLs results in increased

Indexed as

Energy MetabolismOxidative PhosphorylationBiomarkersCell AdhesionCell LineCRISPR-Cas SystemsGene DosageGene EditingGene ExpressionGene Knockdown TechniquesGlycolysisHumansMitochondriaMutationNeoplasmsPhenotypeBiomarkersSDHB protein, humanSuccinate DehydrogenaseGLUD1glutaminehPheo1OXPHOSPCCs/PGLsSDHB

Identifiers

PMID35008989
PMCPMC8745660

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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.