Evidence map›Paper›PMID 28515148›Full record

ArticleCancer research2017

NEMO, a Transcriptional Target of Estrogen and Progesterone, Is Linked to Tumor Suppressor PML in Breast Cancer.

Hanan S Elsarraj, Kelli E Valdez, Yan Hong, Sandra L Grimm, Lawrence R Ricci, Fang Fan, Ossama Tawfik, Lisa May, Therese Cusick, Marc Inciardi and 9 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 13 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

19 authors at 5 institutions in 1 country.

Hanan S ElsarrajDepartment of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, Kansas.
Kelli E ValdezDepartment of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, Kansas.
Yan HongDepartment of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, Kansas.
Sandra L GrimmDepartment of Molecular & Cellular Biology, Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
Lawrence R RicciDepartment of Radiology, Truman Medical Center, Kansas City, Missouri.
Fang FanDepartment of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, Kansas.
Ossama TawfikDepartment of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, Kansas.
Lisa MayDepartment of Radiology, The University of Kansas School of Medicine-Wichita, Wichita, Kansas.
Therese CusickDepartment of Surgery, The University of Kansas School of Medicine-Wichita, Wichita, Kansas.
Marc InciardiDepartment of Radiology, The University of Kansas Medical Center, Kansas City, Kansas.
Mark RedickDepartment of Radiology, The University of Kansas Medical Center, Kansas City, Kansas.
Jason GatewoodDepartment of Radiology, The University of Kansas Medical Center, Kansas City, Kansas.
Onalisa WinbladDepartment of Radiology, The University of Kansas Medical Center, Kansas City, Kansas.
Susan HilsenbeckSmith Breast Center, Baylor College of Medicine, Houston, Texas.
Dean P EdwardsDepartment of Molecular & Cellular Biology, Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
Christy R HaganDepartment of Biochemistry, The University of Kansas Medical Center, Kansas City, Kansas.
Andrew K GodwinDepartment of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, Kansas.
Carol FabianDepartment of Medicine, Breast Cancer Survivorship Center, The University of Kansas Medical Center, Kansas City, Kansas.
Fariba BehbodDepartment of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, Kansas. fbehbod@kumc.edu.
University of Kansas Medical Center · USBaylor College of Medicine · USWichita State University · USThe University of Kansas Cancer Center · USTruman Medical Center · US

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
U KANSAS COBRE ADMINISTRATIVE COREP20RR024214 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI RONGISH, BRENDA J · 2007 to 2011
$10.8M
Novel Approaches for the Control of Microbial PathogensP30GM103326 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI LUTKENHAUS, JOSEPH F · 2012 to 2016
$5.3M
Progression of DCIS to Invasive Breast Cancer through CCR2 Chemokine SignalingR01CA172764 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI CHENG, NIKKI · 2013 to 2024
$4.2M
PROGESTERONE RECEPTOR INTERACTIONR01CA046938 · NCI · UNIVERSITY OF COLORADO DENVER · PI EDWARDS, DEAN P · 1988 to 2013
$3.3M
STEROID ANTAGONISTS AND RESISTANCE IN BREAST CANCERR01DK049030 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI EDWARDS, DEAN P · 1994 to 2012
$3.1M
Identifying the Molecular and Cellular Basis of Invasive Phenotype in Human DCISR01CA207445 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BEHBOD, FARIBA · 2017 to 2019
$1.7M
Role of Cancer Stem Cells in Malignant Progression of Ductal Carcinoma in Situ.R00CA127462 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BEHBOD, FARIBA · 2009 to 2011
$740k
Stem cells and their aberrant self-renewal pathways in DCIS malignant progressionK22CA160587 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI VALDEZ, KELLI E · 2012 to 2014
$379k
(PQC3) Essential Role of BCL9 in Promotion of Human DCIS to Invasive Ductal CarciR21CA185460 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BEHBOD, FARIBA · 2014 to 2015
$361k
Elucidating cellular heterogeneity among cancer stem cells by Raman SpectroscopyR21CA187890 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BEHBOD, FARIBA · 2014 to 2015
$320k
Role of Cancer Stem Cells in Malignant Progression of Ductal Carcinoma in Situ.K99CA127462 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BEHBOD, FARIBA · 2007 to 2008
$272k
NCI NIH HHS K22 CA160587NCI NIH HHS K99 CA127462NCI NIH HHS P30 CA168524NCI NIH HHS R00 CA127462NCI NIH HHS R01 CA046938NCI NIH HHS R01 CA172764NCI NIH HHS R01 CA207445NCI NIH HHS R21 CA185460NCI NIH HHS R21 CA187890NCRR NIH HHS P20 RR024214NIDDK NIH HHS R01 DK049030NIGMS NIH HHS P30 GM103326
6 · The paper itself

Abstract

The beneficial versus detrimental roles of estrogen plus progesterone (E+P) in breast cancer remains controversial. Here we report a beneficial mechanism of E+P treatment in breast cancer cells driven by transcriptional upregulation of the NFκB modulator NEMO, which in turn promotes expression of the tumor suppressor protein promyelocytic leukemia (PML). E+P treatment of patient-derived epithelial cells derived from ductal carcinoma

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorEstrogensFemaleHumansI-kappa B KinaseInterleukin-6Intracellular Signaling Peptides and ProteinsMammary Neoplasms, ExperimentalMCF-7 CellsMiceMice, Inbred NODMice, SCIDProgesteronePromyelocytic Leukemia ProteinEstrogensI-kappa B KinaseIKBKG protein, humanInterleukin-6Intracellular Signaling Peptides and ProteinsNEMO protein, mouseProgesteronePromyelocytic Leukemia ProteinReceptors, EstrogenTumor Suppressor Proteins

Identifiers

PMID28515148
PMCPMC8236416
OpenAlexW2615545145

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.