Evidence map›Paper›PMID 35243806›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Prevention of Tumor Growth and Dissemination by In Situ Vaccination with Mitochondria-Targeted Atovaquone.

Mofei Huang, Donghai Xiong, Jing Pan, Qi Zhang, Yian Wang, Charles R Myers, Bryon D Johnson, Micael Hardy, Balaraman Kalyanaraman, Ming You

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.8field-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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  4. Frontiers in immunology · 2026
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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 3 institutions in 2 countries.

Mofei HuangCenter for Cancer Prevention, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77030, USA.
Donghai XiongCenter for Cancer Prevention, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77030, USA.
Jing PanCenter for Cancer Prevention, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77030, USA.
Qi ZhangCenter for Cancer Prevention, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77030, USA.
Yian WangCenter for Cancer Prevention, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77030, USA.
Charles R MyersDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Bryon D JohnsonDepartment of Medicine, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Micael HardyAix Marseille Univ, CNRS, ICR, UMR 7273, Marseille, 13013, France.
Balaraman KalyanaramanDepartment of Biophysics, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Ming YouCenter for Cancer Prevention, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77030, USA.ORCID 0000-0003-0692-1815
Houston Methodist · USMedical College of Wisconsin · USCentre National de la Recherche Scientifique · FR

Funding

Transfer Application - R01 CA223804 - Chemoimmunoprevention of EGFR-Driven Non-Small Cell Lung CancerR01CA223804 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WANG, LI LILY, YOU, MING · 2018 to 2022
$3.3M
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
NCI NIH HHS R01 CA205633NCI NIH HHS R01 CA223804NCI NIH HHS R01 CA232433NIH HHS R01CA205633NIH HHS R01CA223804NIH HHS R01CA232433
6 · The paper itself

Abstract

Atovaquone, an FDA-approved drug for malaria, is known to inhibit mitochondrial electron transport. A recently synthesized mitochondria-targeted atovaquone increased mitochondrial accumulation and antitumor activity in vitro. Using an in situ vaccination approach, local injection of mitochondria-targeted atovaquone into primary tumors triggered potent T cell immune responses locally and in distant tumor sites. Mitochondria-targeted atovaquone treatment led to significant reductions of both granulocytic myeloid-derived suppressor cells and regulatory T cells in the tumor microenvironment. Mitochondria-targeted atovaquone treatment blocks the expression of genes involved in oxidative phosphorylation and glycolysis in granulocytic-myeloid-derived suppressor cells and regulatory T cells, which may lead to death of granulocytic-myeloid-derived suppressor cells and regulatory T cells. Mitochondria-targeted atovaquone inhibits expression of genes for mitochondrial complex components, oxidative phosphorylation, and glycolysis in both granulocytic-myeloid-derived suppressor cells and regulatory T cells. The resulting decreases in intratumoral granulocytic-myeloid-derived suppressor cells and regulatory T cells could facilitate the observed increase in tumor-infiltrating CD4

Indexed as

NeoplasmsAtovaquoneHumansMitochondriaOxidative PhosphorylationTumor MicroenvironmentVaccinationAtovaquonein situ vaccinationlung cancermitochondrial bioenergeticsmitochondria-targeted atovaquonetumor immune microenvironment

Identifiers

PMID35243806
PMCPMC9036031
OpenAlexW4214823789

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.