Evidence map›Paper›PMID 22158945›Full record

ArticleCancer research2012

S100A7 enhances mammary tumorigenesis through upregulation of inflammatory pathways.

Mohd W Nasser, Zahida Qamri, Yadwinder S Deol, Janani Ravi, Catherine A Powell, Prashant Trikha, Reto A Schwendener, Xue-Feng Bai, Konstantin Shilo, Xianghong Zou and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

82 citing papers in PubMed, 132 citations in OpenAlex.

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  13. S100A5 Attenuates Efficiency of Anti-PD-L1/PD-1 Immunotherapy by Inhibiting CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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22 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 3 countries.

Mohd W NasserDepartment of Pathology, The Ohio State University, Columbus, Ohio 43210, USA.
Zahida Qamri
Yadwinder S Deol
Janani Ravi
Catherine A Powell
Prashant Trikha
Reto A Schwendener
Xue-Feng Bai
Konstantin Shilo
Xianghong Zou
Gustavo Leone
Ronald Wolf
Stuart H Yuspa
Ramesh K Ganju
Ludwig-Maximilians-Universität München · DENational Cancer Institute · USCancer Genetics (United States) · USUniversity of Zurich · CH

Funding

Suppression of Mammary Tumorigenesis by Stromal p53P01CA097189 · NCI · OHIO STATE UNIVERSITY · PI FERNANDEZ, SOLEDAD A · 2004 to 2016
$16.1M
Role of Slit in CXCR4-Mediated Breast Cancer MetastasisR01CA109527 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2005 to 2019
$2.6M
Role of S100A7 in breast cancer progression and metastasisR01CA153490 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2011 to 2014
$1.2M
The role of CD200 in T cell therapy of cancerR01CA138427 · NCI · OHIO STATE UNIVERSITY · PI BAI, XUE-FENG · 2009 to 2012
$981k
NCI NIH HHS CA109527NCI NIH HHS CA153490NCI NIH HHS P01 CA097189NCI NIH HHS R01 CA109527NCI NIH HHS R01 CA138427NCI NIH HHS R01 CA153490
6 · The paper itself

Abstract

S100A7/psoriasin, a member of the epidermal differentiation complex, is widely overexpressed in invasive estrogen receptor (ER)α-negative breast cancers. However, it has not been established whether S100A7 contributes to breast cancer growth or metastasis. Here, we report the consequences of its expression on inflammatory pathways that impact breast cancer growth. Overexpression of human S100A7 or its murine homologue mS100a7a15 enhanced cell proliferation and upregulated various proinflammatory molecules in ERα-negative breast cancer cells. To examine in vivo effects, we generated mice with an inducible form of mS100a7a15 (MMTV-mS100a7a15 mice). Orthotopic implantation of MVT-1 breast tumor cells into the mammary glands of these mice enhanced tumor growth and metastasis. Compared with uninduced transgenic control mice, the mammary glands of mice where mS100a7a15 was induced exhibited increased ductal hyperplasia and expression of molecules involved in proliferation, signaling, tissue remodeling, and macrophage recruitment. Furthermore, tumors and lung tissues obtained from these mice showed further increases in prometastatic gene expression and recruitment of tumor-associated macrophages (TAM). Notably, in vivo depletion of TAM inhibited the effects of mS100a7a15 induction on tumor growth and angiogenesis. Furthermore, introduction of soluble hS100A7 or mS100a7a15 enhanced chemotaxis of macrophages via activation of RAGE receptors. In summary, our work used a powerful new model system to show that S100A7 enhances breast tumor growth and metastasis by activating proinflammatory and metastatic pathways.

Indexed as

AnimalsBlotting, WesternBreast NeoplasmsCell Line, TumorCell ProliferationChemokinesChemotaxisCytokinesFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansInflammationMacrophagesMaleMammary Neoplasms, ExperimentalChemokinesCytokinesReceptor for Advanced Glycation End ProductsReceptors, ImmunologicS100a7a protein, mouseS100A7 protein, humanS100 Calcium Binding Protein A7S100 ProteinsVascular Endothelial Growth Factor A

Identifiers

PMID22158945
PMCPMC3271140
OpenAlexW2167873562

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.