Evidence map›Paper›PMID 27967239›Full record

ArticleEndocrinology2017

Lipid Osteoclastokines Regulate Breast Cancer Bone Metastasis.

Jing Y Krzeszinski, Adam G Schwaid, Wing Yin Cheng, Zixue Jin, Zachary R Gallegos, Alan Saghatelian, Yihong Wan

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  15. Targeting the Wnt signaling pathway for breast cancer bone metastasis therapy.Journal of molecular medicine (Berlin, Germany) · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jing Y KrzeszinskiDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, USA.
Adam G SchwaidDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts.
Wing Yin ChengDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, USA.
Zixue JinDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, USA.
Zachary R GallegosDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, USA.
Alan SaghatelianDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts.
Yihong WanDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, USA.
Harvard University · USThe University of Texas Southwestern Medical Center · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
Connection of Mineral and Energy Metabolism by the Nuclear Receptor PPAR-gammaR01DK089113 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI WAN, YIHONG · 2011 to 2015
$1.8M
Novel extra cellular RNA-based combinatorial RNA inhibition therapyUH2TR000943 · NCATS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CALIN, GEORGE A., LOPEZ-BERESTEIN, GABRIEL · 2013 to 2014
$1.1M
NCATS NIH HHS UH2 TR000943NCI NIH HHS P30 CA014195NCI NIH HHS P30 CA142543NIDDK NIH HHS R01 DK089113
6 · The paper itself

Abstract

Bone metastasis is a deadly consequence of cancers, in which osteoclast forms a vicious cycle with tumor cells. Bone metastasis attenuation by clinical usage of osteoclast inhibitors and in our osteopetrotic mouse genetic models with β-catenin constitutive activation or peroxisome proliferator-activated receptor γ deficiency fully support the important role of osteoclast in driving the bone metastatic niche. However, the mechanisms for this "partnership in crime" are underexplored. Here we show that osteoclasts reprogram their lipid secretion to support cancer cells. Metabolomic profiling reveals elevated prometastatic arachidonic acid (AA) but reduced antimetastatic lysophosphatidylcholines (LPCs). This shift in lipid osteoclastokines synergistically stimulates tumor cell proliferation, migration, survival, and expression of prometastatic genes. Pharmacologically, combined treatment with LPCs and BW-755C, an inhibitor of AA signaling via blocking lipoxygenase and cyclooxygenase, impedes breast cancer bone metastasis. Our findings elucidate key paracrine mechanisms for the osteoclast-cancer vicious cycle and uncover important therapeutic targets for bone metastasis.

Indexed as

Lipid MetabolismAnimalsArachidonic AcidBone NeoplasmsBreast NeoplasmsCell MovementCytokinesFemaleLysophosphatidylcholinesMetabolomicsMice, KnockoutMice, NudeNeoplasm MetastasisNeoplasm TransplantationOsteoclastsOsteogenesisArachidonic AcidCytokinesLysophosphatidylcholines

Identifiers

PMID27967239
PMCPMC5460780
OpenAlexW2564885696

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.