Evidence map›Paper›PMID 31848195›Full record

ArticleCancer research2020

Mitochondrial Haplotype of the Host Stromal Microenvironment Alters Metastasis in a Non-cell Autonomous Manner.

Amanda E Brinker, Carolyn J Vivian, Thomas C Beadnell, Devin C Koestler, Shao Thing Teoh, Sophia Y Lunt, Danny R Welch

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

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  14. Mechanisms of breast cancer metastasis.Clinical & experimental metastasis · 2022
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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

7 authors at 2 institutions in 2 countries.

Amanda E BrinkerDepartment of Cancer Biology, The University of Kansas Medical Center, Kansas City, Kansas.ORCID 0000-0003-1134-0572
Carolyn J VivianDepartment of Cancer Biology, The University of Kansas Medical Center, Kansas City, Kansas.
Thomas C BeadnellDepartment of Cancer Biology, The University of Kansas Medical Center, Kansas City, Kansas.
Devin C KoestlerThe University Kansas Cancer Center, The University of Kansas Medical Center, Kansas City, Kansas.
Shao Thing TeohDepartment of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan.ORCID 0000-0002-5938-258X
Sophia Y LuntDepartment of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan.ORCID 0000-0003-4522-6065
Danny R WelchDepartment of Cancer Biology, The University of Kansas Medical Center, Kansas City, Kansas. dwelch@kumc.edu.ORCID 0000-0002-1951-4947
The University of Kansas Cancer Center · USMichigan State University · US

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SUSAN J. BROWN · 2012 to 2026
$63.0M
Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NICOLE L NOLLEN · 2012 to 2026
$40.1M
Using Integrated Omics to Identify Dysfunctional Genetic Mechanisms Influencing Schizophrenia and Sleep DisturbancesP20GM130423 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ANDREW K. GODWIN · 2019 to 2026
$21.5M
KISS1: Defining Mechanisms for Antimetastatic TherapyR01CA134981 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI WELCH, DANNY R. · 2009 to 2014
$1.5M
NCI NIH HHS P30 CA168524NCI NIH HHS R01 CA134981NIGMS NIH HHS P20 GM103418NIGMS NIH HHS P20 GM130423
6 · The paper itself

Abstract

Mitochondria contribute to tumor growth through multiple metabolic pathways, regulation of extracellular pH, calcium signaling, and apoptosis. Using the Mitochondrial Nuclear Exchange (MNX) mouse models, which pair nuclear genomes with different mitochondrial genomes, we previously showed that mitochondrial SNPs regulate mammary carcinoma tumorigenicity and metastatic potential in genetic crosses. Here, we tested the hypothesis that polymorphisms in stroma significantly affect tumorigenicity and experimental lung metastasis. Using syngeneic cancer cells (EO771 mammary carcinoma and B16-F10 melanoma cells) injected into wild-type and MNX mice (i.e., same nuclear DNA but different mitochondrial DNA), we showed mt-SNP-dependent increases (C3H/HeN) or decreases (C57BL/6J) in experimental metastasis. Superoxide scavenging reduced experimental metastasis. In addition, expression of lung nuclear-encoded genes changed specifically with mt-SNP. Thus, mitochondrial-nuclear cross-talk alters nuclear-encoded signaling pathways that mediate metastasis via both intrinsic and extrinsic mechanisms. SIGNIFICANCE: Stromal mitochondrial polymorphisms affect metastatic colonization through reactive oxygen species and mitochondrial-nuclear cross-talk.

Indexed as

AnimalsBreast NeoplasmsCarcinogenesisCell Line, TumorCell NucleusDisease Models, AnimalDNA, MitochondrialFemaleHaplotypesHumansLung NeoplasmsMaleMiceMice, Inbred StrainsMitochondriaNeoplasm MetastasisDNA, MitochondrialSuperoxides

Identifiers

PMID31848195
PMCPMC7056497
OpenAlexW2996656274

What OpenQuestion holds

Textmetadata
LicenceTDM
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.