Evidence map›Paper›PMID 29162724›Full record

ArticleThe Journal of biological chemistry2018

Progesterone receptor A promotes invasiveness and metastasis of luminal breast cancer by suppressing regulation of critical microRNAs by estrogen.

Thomas McFall, Brooke McKnight, Rayna Rosati, Seongho Kim, Yanfang Huang, Nerissa Viola-Villegas, Manohar Ratnam

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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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 1 country.

Thomas McFallFrom the Barbara Ann Karmanos Cancer Institute and Department of Oncology, Wayne State University, Detroit, Michigan 48201-2013.
Brooke McKnightFrom the Barbara Ann Karmanos Cancer Institute and Department of Oncology, Wayne State University, Detroit, Michigan 48201-2013.
Rayna RosatiFrom the Barbara Ann Karmanos Cancer Institute and Department of Oncology, Wayne State University, Detroit, Michigan 48201-2013.
Seongho KimFrom the Barbara Ann Karmanos Cancer Institute and Department of Oncology, Wayne State University, Detroit, Michigan 48201-2013.
Yanfang HuangFrom the Barbara Ann Karmanos Cancer Institute and Department of Oncology, Wayne State University, Detroit, Michigan 48201-2013.
Nerissa Viola-VillegasFrom the Barbara Ann Karmanos Cancer Institute and Department of Oncology, Wayne State University, Detroit, Michigan 48201-2013.
Manohar RatnamFrom the Barbara Ann Karmanos Cancer Institute and Department of Oncology, Wayne State University, Detroit, Michigan 48201-2013 ratnamm@karmanos.org.
The Barbara Ann Karmanos Cancer Institute · USWayne State University · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
Salk Institute Cancer Training GrantT32CA009370 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Diana Clare Hargreaves, Jan Karlseder · 1986 to 2026
$8.6M
TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
Dissecting the Mechanisms of Tamoxifen ActionR01CA140690 · NCI · WAYNE STATE UNIVERSITY · PI RATNAM, MANOHAR · 2009 to 2013
$1.5M
NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA140690NCI NIH HHS T32 CA009370NCI NIH HHS T32 CA009531
6 · The paper itself

Abstract

Distal metastasis of luminal breast cancer is frequent and incurable, yet the metastasis mechanisms are poorly understood. Estrogen, even at postmenopausal concentrations, suppresses invasiveness of luminal breast cancer cells through the estrogen receptor (ER). Invasive tumors overexpress the short progesterone receptor A (PR-A) isoform. Even at postmenopausal concentrations, progesterone activates PR-A, inducing invasiveness by counteracting estrogen's effects, particularly when cells are hypersensitized to progesterone by PR-A overexpression. To interrogate the role of this cross-talk in metastasis, we investigated selective cross-talk mechanisms of PR-A with ER. We developed a quantitative PCR-based lymph node infiltration assay to address the slowness of metastasis of tumor xenografts. We found that 15 microRNAs (miRNAs) are regulated by progesterone via PR-A, but not the longer PR-B isoform, with increased progesterone sensitivity when PR-A was overexpressed. Two of these miRNAs whose induction (miR-92a-3p) or repression (miR-26b-5p) by estrogen was suppressed by progesterone plus PR-A were critical for the PR-A-ER cross-talk causing a gene-regulatory pattern of invasiveness and metastasis and complete rescue of invasiveness

Indexed as

Biomarkers, TumorBreast NeoplasmsEstrogensFemaleHumansMicroRNAsNeoplasm InvasivenessNeoplasm MetastasisNeoplasm ProteinsReceptors, ProgesteroneRNA, NeoplasmBiomarkers, TumorEstrogensMicroRNAsMIRN26 microRNA, humanMIRN92 microRNA, humanNeoplasm Proteinsprogesterone receptor AReceptors, ProgesteroneRNA, Neoplasmcell invasionestrogenestrogen receptorluminal breast cancermicroRNA (miRNA)progesteroneprogesterone receptortumor metastasis

Identifiers

PMID29162724
PMCPMC5787796
OpenAlexW2768561243

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.