Evidence map›Paper›PMID 19261859›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

PML depletion disrupts normal mammary gland development and skews the composition of the mammary luminal cell progenitor pool.

Wenjing Li, Brian J Ferguson, Walid T Khaled, Maxine Tevendale, John Stingl, Valeria Poli, Tina Rich, Paolo Salomoni, Christine J Watson

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 53 citations in OpenAlex.

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  16. Tumor suppressive pathways in the control of neurogenesis.Cellular and molecular life sciences : CMLS · 2013
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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

9 authors at 2 institutions in 2 countries.

Wenjing LiDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, United Kingdom.
Brian J Ferguson
Walid T Khaled
Maxine Tevendale
John Stingl
Valeria Poli
Tina Rich
Paolo Salomoni
Christine J Watson
University of Cambridge · GBUniversity of Turin · IT

Funding

Biotechnology and Biological Sciences Research Council BB/D012937/1Breast Cancer Now 2006NOVPHD11Medical Research Council MC_U132670601
6 · The paper itself

Abstract

Nuclear domains of promyelocytic leukemia protein (PML) are known to act as signaling nodes in many cellular processes. Although the impact of PML expression in driving cell fate decisions for injured cells is well established, the function of PML in the context of tissue development is less well understood. Here, the in vivo role of PML in developmental processes in the murine mammary gland has been investigated. Data are presented showing that expression of PML is tightly regulated by three members of the Stat family of transcription factors that orchestrate the functional development of the mammary secretory epithelium during pregnancy. Developmental phenotypes were also discovered in the virgin and pregnant Pml null mouse, typified by aberrant differentiation of mammary epithelia with reduced ductal and alveolar development. PML depletion was also found to disturb the balance of two distinct luminal progenitor populations. Overall, it is shown that PML is required for cell lineage determination in bi-potent luminal progenitor cells and that the precise regulation of PML expression is required for functional differentiation of alveolar cells.

Indexed as

AnimalsCell DifferentiationEpithelial CellsFemaleGene Expression Regulation, DevelopmentalMammary Glands, AnimalMiceMorphogenesisNuclear ProteinsPromyelocytic Leukemia ProteinSTAT Transcription FactorsStem CellsTranscription FactorsTranscription, GeneticTumor Suppressor ProteinsNuclear ProteinsPml protein, mousePromyelocytic Leukemia ProteinSTAT Transcription FactorsTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID19261859
PMCPMC2660741
OpenAlexW2128390703

What OpenQuestion holds

Textmetadata
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.