Evidence map›Paper›PMID 32843660›Full record

ArticleScientific reports2020

Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth.

Gyula Bencze, Szilvia Bencze, Keith D Rivera, James D Watson, Mate Hidvegi, Laszlo Orfi, Nicholas K Tonks, Darryl J Pappin

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Hederagenin Induces Apoptosis of Human Hepatoma HepG2 CellsCombinatorial chemistry & high throughput screening · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Of mitochondrion and COVID-19.Journal of enzyme inhibition and medicinal chemistry · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Gyula BenczeCold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA. benczegyula@gmail.com.
Szilvia BenczeCold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
Keith D RiveraCold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
James D WatsonCold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
Mate HidvegiJewish Theological Seminary-University of Jewish Studies, Budapest, 1084, Hungary.
Laszlo OrfiDepartment of Pharmaceutical Chemistry, Semmelweis University, Budapest, 1085, Hungary.
Nicholas K TonksCold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
Darryl J PappinCold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
Cold Spring Harbor Laboratory · USBudapest University of Jewish Studies · HUSemmelweis University · HU

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI John Edward Moses · 1987 to 2026
$118.9M
PROTEIN TYROSINE DEPHOSPHORYLATION &SIGNAL TRANSDUCTIONR01CA053840 · NCI · COLD SPRING HARBOR LABORATORY · PI TONKS, NICHOLAS K · 1991 to 2025
$11.8M
NCI NIH HHS P30 CA045508NCI NIH HHS R01 CA053840
6 · The paper itself

Abstract

Mitochondrial dysfunction and significant changes in metabolic pathways accompany cancer development and are responsible for maintaining the tumor microenvironment. Normal mitochondria can trigger intrinsic apoptosis by releasing cytochrome c into the cytosol. The survival of malignant cells highly depends on the suppression of this function. We validated that A250, a highly purified fraction of fermented wheat germ extract (FWGE), increases the carbon flux into the mitochondria, the expression of key elements of the Krebs cycle and oxidative phosphorylation (OXPHOS). The increased respiratory chain activity is related to the mitochondria's ability to release cytochrome c into the cytosol, which triggers the apoptotic cascade. The 68% tumor growth inhibitory effect observed in the murine melanoma study is related to this effect, as proteomic analysis validated similar changes in mitochondrial protein levels in the isolated tumor tissue samples. Blood count data indicated that this effect was not accompanied by general toxicity. This study is significant, as it shows that a highly concentrated form of FWGE is an effective agent that increases normal mitochondrial functionality. The lack of hepatotoxic and general toxic effects makes A250 an excellent candidate targeting mitochondria function in cancer therapy.

Indexed as

AnimalsApoptosisCarbonCell Line, TumorCitric Acid CycleCytochromes cDrug Screening Assays, AntitumorFermentationGene Expression Regulation, NeoplasticHEK293 CellsHumansLiverMelanoma, ExperimentalMethanolMiceMitochondriaCarbonCytochromes cMethanolPlant ExtractsSolvents

Identifiers

PMID32843660
PMCPMC7447799
OpenAlexW3080259521

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.