Evidence map›Paper›PMID 31040372›Full record

ArticleScientific reports2019

Reduced Basal Nitric Oxide Production Induces Precancerous Mammary Lesions via ERBB2 and TGFβ.

Gang Ren, Xunzhen Zheng, Matthew Bommarito, Samantha Metzger, Yashna Walia, Joshua Letson, Allen Schroering, Andrea Kalinoski, David Weaver, Christopher Figy and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  12. S-Nitrosylation in Tumor Microenvironment.International journal of molecular sciences · 2021
    Review
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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

12 authors at 1 institution in 1 country.

Gang RenUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA.
Xunzhen ZhengUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA.
Matthew BommaritoUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA.
Samantha MetzgerUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA.
Yashna WaliaUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA.
Joshua LetsonUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA.
Allen SchroeringUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Surgery, 3000 Arlington Ave, MS1008, Toledo, OH, USA.
Andrea KalinoskiUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Surgery, 3000 Arlington Ave, MS1008, Toledo, OH, USA.
David WeaverUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Surgery, 3000 Arlington Ave, MS1008, Toledo, OH, USA.
Christopher FigyUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA.
Kam YeungUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA.
Saori FurutaUniversity of Toledo Health Science Campus, College of Medicine and Life Sciences, Department of Cancer Biology, 3000 Arlington Ave, MS1010, Toledo, OH, USA. saori.furuta@utoledo.edu.ORCID http://orcid.org/0000-0003-1121-0487
University of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One third of newly diagnosed breast cancers in the US are early-stage lesions. The etiological understanding and treatment of these lesions have become major clinical challenges. Because breast cancer risk factors are often linked to aberrant nitric oxide (NO) production, we hypothesized that abnormal NO levels might contribute to the formation of early-stage breast lesions. We recently reported that the basal level of NO in the normal breast epithelia plays crucial roles in tissue homeostasis, whereas its reduction contributes to the malignant phenotype of cancer cells. Here, we show that the basal level of NO in breast cells plummets during cancer progression due to reduction of the NO synthase cofactor, BH

Indexed as

AnimalsBiomarkersBreastBreast NeoplasmsDisease SusceptibilityEpithelial CellsErb-b2 Receptor Tyrosine KinasesFemaleGene ExpressionHumansMiceNeoplastic Stem CellsNitric OxideNitric Oxide Synthase Type INitric Oxide Synthase Type IINitric Oxide Synthase Type IIIBiomarkersERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesNitric OxideNitric Oxide Synthase Type INitric Oxide Synthase Type IINitric Oxide Synthase Type IIINOS2 protein, humanNOS3 protein, humanTransforming Growth Factor beta

Identifiers

PMID31040372
PMCPMC6491486
OpenAlexW2942527732

What Socratic 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 Socratic graph.