Evidence map›Paper›PMID 26862086›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2016

Mammary Adipose Tissue-Derived Lysophospholipids Promote Estrogen Receptor-Negative Mammary Epithelial Cell Proliferation.

Paul A Volden, Maxwell N Skor, Marianna B Johnson, Puneet Singh, Feenalie N Patel, Martha K McClintock, Matthew J Brady, Suzanne D Conzen

Open access · greenAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  10. The pleiotropic roles of adipocyte secretome in remodeling breast cancer.Journal of experimental & clinical cancer research : CR · 2022
    Review
  11. Article
  12. Review
  13. Drivers and suppressors of triple-negative breast cancer.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Cancer-associated adipocytes: emerging supporters in breast cancer.Journal of experimental & clinical cancer research : CR · 2020
    Review
  19. Review
  20. Article
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

8 authors at 1 institution in 1 country.

Paul A VoldenDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Maxwell N SkorDepartment of Medicine, The University of Chicago, Chicago, Illinois. Committee on Molecular Metabolism and Nutrition, The University of Chicago, Chicago, Illinois.
Marianna B JohnsonDepartment of Medicine, The University of Chicago, Chicago, Illinois.
Puneet Singh
Feenalie N Patel
Martha K McClintockDepartment of Psychology, The University of Chicago, Chicago, Illinois. Institute for Mind and Biology, The University of Chicago, Chicago, Illinois.
Matthew J BradyDepartment of Medicine, The University of Chicago, Chicago, Illinois. Committee on Molecular Metabolism and Nutrition, The University of Chicago, Chicago, Illinois. sdconzen@uchicago.edu mbrady@medicine.bsd.uchicago.edu.
Suzanne D ConzenDepartment of Medicine, The University of Chicago, Chicago, Illinois. Committee on Molecular Metabolism and Nutrition, The University of Chicago, Chicago, Illinois. Institute for Mind and Biology, The University of Chicago, Chicago, Illinois. Ben May Department of Cancer Research, The University of Chicago, Chicago, Illinois. sdconzen@uchicago.edu mbrady@medicine.bsd.uchicago.edu.
University of Chicago · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SUSAN J. BROWN · 2012 to 2026
$63.0M
Pilot and Feasibility ProgramP30DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI Matthew J Brady · 2013 to 2026
$20.9M
Multi-Disciplinary Training Grant in Cancer ResearchT32CA009594 · NCI · UNIVERSITY OF CHICAGO · PI KAY F MACLEOD, Scott A. Oakes · 1989 to 2026
$11.5M
Identifying mechanisms linking stress biology to human breast cancerR01CA148814 · NCI · UNIVERSITY OF CHICAGO · PI CONZEN, SUZANNE DANIELA, MCCLINTOCK, MARTHA KENT · 2011 to 2015
$1.6M
An Interdisciplinary Molecular Metabolism Training ProgramT32DK087703 · NIDDK · UNIVERSITY OF CHICAGO · PI RHODES, CHRISTOPHER J · 2010 to 2014
$709k
Triple Quadrupole - Ion Trap Hybrid LC/MS/MS SystemS10RR027926 · NCRR · WAYNE STATE UNIVERSITY · PI MADDIPATI, KRISHNARAO · 2010 to 2010
$425k
NCI NIH HHS P30 CA014599NCI NIH HHS R01 CA148814NCI NIH HHS T32 CA009594NCRR NIH HHS S10 RR027926NIDDK NIH HHS P30 DK020595NIDDK NIH HHS T32 DK087703NIGMS NIH HHS P20 GM103418
6 · The paper itself

Abstract

Lysophosphatidic acid (LPA), acting in an autocrine or paracrine fashion through G protein-coupled receptors, has been implicated in many physiologic and pathologic processes, including cancer. LPA is converted from lysophosphatidylcholine (LPC) by the secreted phospholipase autotaxin (ATX). Although various cell types can produce ATX, adipocyte-derived ATX is believed to be the major source of circulating ATX and also to be the major regulator of plasma LPA levels. In addition to ATX, adipocytes secrete numerous other factors (adipokines); although several adipokines have been implicated in breast cancer biology, the contribution of mammary adipose tissue-derived LPC/ATX/LPA (LPA axis) signaling to breast cancer is poorly understood. Using murine mammary fat-conditioned medium, we investigated the contribution of LPA signaling to mammary epithelial cancer cell biology and identified LPA signaling as a significant contributor to the oncogenic effects of the mammary adipose tissue secretome. To interrogate the role of mammary fat in the LPA axis during breast cancer progression, we exposed mammary adipose tissue to secreted factors from estrogen receptor-negative mammary epithelial cell lines and monitored changes in the mammary fat pad LPA axis. Our data indicate that bidirectional interactions between mammary cancer cells and mammary adipocytes alter the local LPA axis and increase ATX expression in the mammary fat pad during breast cancer progression. Thus, the LPC/ATX/LPA axis may be a useful target for prevention in patients at risk of ER-negative breast cancer. Cancer Prev Res; 9(5); 367-78. ©2016 AACR.

Indexed as

Adipose TissueAnimalsCell ProliferationCulture Media, ConditionedEpithelial CellsFemaleImmunohistochemistryLysophospholipidsMammary Glands, AnimalMammary Neoplasms, ExperimentalMiceReal-Time Polymerase Chain ReactionReceptors, EstrogenSignal TransductionCulture Media, ConditionedLysophospholipidsReceptors, Estrogen

Identifiers

PMID26862086
PMCPMC4854771
OpenAlexW2265152164

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.