Evidence map›Paper›PMID 32010429›Full record

ArticleOncotarget2020

Sequence conservation of mitochondrial (mt)DNA during expansion of clonal mammary epithelial populations suggests a common mtDNA template in CzechII mice.

Jabril R Johnson, Justin B Lack, Corinne A Boulanger, Lauren E Ragle, Gilbert H Smith

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 100% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 3 institutions in 1 country.

Jabril R JohnsonMammary Stem Cell Biology Section, National Cancer Institute, Bethesda, MD 20892, USA.
Justin B LackBioinformatics Manager/Lead, NIAID Collaborative Bioinformatics Resource (NCBR) Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Bethesda, MD 20894, USA.
Corinne A BoulangerMammary Stem Cell Biology Section, National Cancer Institute, Bethesda, MD 20892, USA.
Lauren E RagleMammary Stem Cell Biology Section, National Cancer Institute, Bethesda, MD 20892, USA.
Gilbert H SmithMammary Stem Cell Biology Section, National Cancer Institute, Bethesda, MD 20892, USA.
National Cancer Institute · USCity of Hope · USFrederick National Laboratory for Cancer Research · US

Funding

Biology of Mammary Gland Development and TumorigenesisZIABC010021 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SMITH, GILBERT · 2009 to 2020
$11.6M
6 · The paper itself

Abstract

One major foundation of cancer etiology is the process of clonal expansion. The mechanisms underlying the complex process of a single cell leading to a clonal dominant tumor, are poorly understood. Our study aims to analyze mitochondrial DNA (mtDNA) for somatic single nucleotide polymorphisms (SNPs) variants, to determine if they are conserved throughout clonal expansion in mammary tissues and tumors. To test this hypothesis, we took advantage of a mouse mammary tumor virus (MMTV)-infected mouse model (CzechII). CzechII mouse mtDNA was extracted, from snap-frozen normal, hyperplastic, and tumor mammary epithelial outgrowth fragments. Next generation deep sequencing was used to determine if mtDNA "

Indexed as

clonal expansionmammary cancermitochondrial DNAnext-generation sequencing

Identifiers

PMID32010429
PMCPMC6968779
OpenAlexW3000289648

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.