Evidence map›Paper›PMID 31336167›Full record

ArticleMechanisms of development2019

Long-label-retaining mammary epithelial cells are created early in ductal development and distributed throughout the branching ducts.

Lauren E Ragle, Robert D Bruno, Corinne A Boulanger, Gilbert H Smith

Open access · greenAbstract read
In one paragraph

Article in Mechanisms of development, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
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

4 authors at 2 institutions in 1 country.

Lauren E RagleMammary Stem Cell Section, BRL, CCR, National Cancer Institute, Bethesda, MD 20892, United States of America.
Robert D BrunoSchool of Medical Diagnostic and Translational Sciences, College of Health Sciences, Old Dominion University, Norfolk, VA 23529, United States of America.
Corinne A BoulangerMammary Stem Cell Section, BRL, CCR, National Cancer Institute, Bethesda, MD 20892, United States of America.
Gilbert H SmithMammary Stem Cell Section, BRL, CCR, National Cancer Institute, Bethesda, MD 20892, United States of America. Electronic address: smithg@mail.nih.gov.
National Cancer Institute · USOld Dominion University · US

Funding

Biology of Mammary Gland Development and TumorigenesisZIABC010021 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SMITH, GILBERT · 2009 to 2020
$11.6M
Mammary Gland Development and TumorigenesisZ01BC010021 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SMITH, GILBERT · 1996 to 2008
$1.8M
Intramural NIH HHS Z01 BC010021
6 · The paper itself

Abstract

Long-label retention has been used by many to prove Cairns' immortal strand hypothesis and to identify potential stem cells. Here, we describe two strategies using 5-ethynl-2'-deoxyuridine (EdU) to identify and understand the distribution of long-label-retaining mammary epithelial cells during formation of the mouse mammary ductal system. First, EdU was given upon two consecutive days per week during weeks 4 through 10 and analyzed for label retention at 13 weeks of age. Alternatively, EdU was given for 14 consecutive days beginning at 28 days of age and ending at 42 days of age. Analyses were conducted at >91 days of age (13 weeks). Many more LREC were detected following the second labeling method and their distribution among the subsequently developed ducts. This finding indicated that the early-labeled cells that retained their label were distributed into portions of the gland that developed after the ending of EdU treatment (i.e. 42->91 days). These observations may have important meaning with respect to the previously demonstrated retention of regenerative capacity throughout the mouse mammary gland despite age or reproductive history. These results suggest LREC may represent long-lived progenitor cells that are responsible for mammary gland homeostasis. Additionally, these cells may act as multipotent stem cells capable of mammary gland regeneration upon random fragment transplantation into epithelium-denuded mammary fat pads.

Indexed as

OrganogenesisAnimalsEpithelial CellsFemaleG2 PhaseMammary Glands, AnimalMice, Inbred BALB CMice, NudeStaining and LabelingDevelopmentEDU-labelingLong-label-retainingMammaryStem cell

Identifiers

PMID31336167
PMCPMC6759405
OpenAlexW2963043814

What OpenQuestion holds

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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.