Evidence map›Paper›PMID 32264893›Full record

ArticleCell communication and signaling : CCS2020

Magnolia extract is effective for the chemoprevention of oral cancer through its ability to inhibit mitochondrial respiration at complex I.

Qi Zhang, Gang Cheng, Jing Pan, Jacek Zielonka, Donghai Xiong, Charles R Myers, Liang Feng, Song Seok Shin, Young Heui Kim, Dinh Bui and 6 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Cell communication and signaling : CCS, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  4. Small molecule probes for peroxynitrite detection.Redox biochemistry and chemistry · 2024
    Article
  5. Review
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  11. Cancer chemoprevention with PV-1, a novelFrontiers in immunology · 2023
    Article
  12. Review
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  15. Article
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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

16 authors at 3 institutions in 1 country.

Qi ZhangCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Gang ChengCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Jing PanCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Jacek ZielonkaCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Donghai XiongCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Charles R MyersCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Liang FengCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Song Seok ShinLife Science R&D Center, Osong, Cheongju, South Korea.
Young Heui KimLife Science R&D Center, Osong, Cheongju, South Korea.
Dinh BuiCollege of Pharmacy, University of Houston, Houston, TX, 77204-5037, USA.
Ming HuCollege of Pharmacy, University of Houston, Houston, TX, 77204-5037, USA.
Brian BennettDepartment of Physics, Marquette University, Milwaukee, WI, 53233, USA.
Kathleen SchmaindaDepartment of Biophysics, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Yian WangCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Balaraman KalyanaramanCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Ming YouCenter for Disease Prevention Research, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA. myou@mcw.edu.ORCID 0000-0002-9741-268X
Medical College of Wisconsin · USUniversity of Houston · USMarquette University · US

Funding

Chemoprevention of Lung Cancer with Mitochondria-Targeted HonokiolR01CA208648 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI KALYANARAMAN, BALARAMAN, YOU, MING · 2017 to 2021
$3.1M
Inhibition of Oral Tumorigenesis by Antitumor BR01CA205633 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI HU, MING, WONG, STUART J · 2017 to 2022
$2.6M
Chemoprevention of lung cancer by targeting lonidamine to mitochondriaR01CA232433 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI KALYANARAMAN, BALARAMAN, KRESTY, LAURA A · 2019 to 2023
$2.0M
Mitochondria-targeted Agents in Breast CancerR01CA152810 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI KALYANARAMAN, BALARAMAN · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA152810NCI NIH HHS R01 CA205633NCI NIH HHS R01 CA208648NCI NIH HHS R01 CA232433
6 · The paper itself

Abstract

backgroundMagnolia extract (ME) is known to inhibit cancer growth and metastasis in several cell types in vitro and in animal models. However, there is no detailed study on the preventive efficacy of ME for oral cancer, and the key components in ME and their exact mechanisms of action are not clear. The overall goal of this study is to characterize ME preclinically as a potent oral cancer chemopreventive agent and to determine the key components and their molecular mechanism(s) that underlie its chemopreventive efficacy.

methodsThe antitumor efficacy of ME in oral cancer was investigated in a 4-nitroquinoline-1-oxide (4NQO)-induced mouse model and in two oral cancer orthotopic models. The effects of ME on mitochondrial electron transport chain activity and ROS production in mouse oral tumors was also investigated.

resultsME did not cause detectable side effects indicating that it is a promising and safe chemopreventive agent for oral cancer. Three major key active compounds in ME (honokiol, magnolol and 4-O-methylhonokiol) contribute to its chemopreventive effects. ME inhibits mitochondrial respiration at complex I of the electron transport chain, oxidizes peroxiredoxins, activates AMPK, and inhibits STAT3 phosphorylation, resulting in inhibition of the growth and proliferation of oral cancer cells.

conclusionOur data using highly relevant preclinical oral cancer models, which share histopathological features seen in human oral carcinogenesis, suggest a novel signaling and regulatory role for mitochondria-generated superoxide and hydrogen peroxide in suppressing oral cancer cell proliferation, progression, and metastasis. Video abstract.

Indexed as

Antineoplastic Agents, PhytogenicBiphenyl CompoundsLignansPlant ExtractsAllyl CompoundsAnimalsCell Line, TumorDrug Evaluation, PreclinicalFemaleHumansMagnoliaMiceMice, NudeMitochondriaMouth NeoplasmsPhenols4-O-methylhonokiolAllyl CompoundsAntineoplastic Agents, PhytogenicBiphenyl CompoundshonokiolLignansmagnololPhenolsPlant ExtractsReactive Oxygen SpeciesAMPKComplex IOral cancerSTAT3

Identifiers

PMID32264893
PMCPMC7140380
OpenAlexW3015057565

What OpenQuestion holds

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LicenceCC BY
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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.