Evidence map›Paper›PMID 26696367›Full record

ArticleNeoplasia (New York, N.Y.)2015

Breast Cancer Cell Colonization of the Human Bone Marrow Adipose Tissue Niche.

Zach S Templeton, Wen-Rong Lie, Weiqi Wang, Yael Rosenberg-Hasson, Rajiv V Alluri, John S Tamaresis, Michael H Bachmann, Kitty Lee, William J Maloney, Christopher H Contag and 1 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 3% 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

80 citing papers in PubMed, 2 syntheses or guidelines pooled it, 118 citations in OpenAlex.

  1. Pooled it
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  6. Autophagy · 2026
    Article
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  19. Article
  20. Update on Adipose Tissue and Cancer.Endocrine reviews · 2023
    Article

20 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

11 authors at 1 institution in 1 country.

Zach S TempletonDepartment of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427. Electronic address: zstemple@stanford.edu.
Wen-Rong LieEMD Millipore Corporation, 14 Research Park Drive, St Charles, MO 63304-5618. Electronic address: Wen-rong.lie@emdmillipore.com.
Weiqi WangDepartment of Immunology, Fairchild Science Building, D033, 299 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5124. Electronic address: Weiqi@stanford.edu.
Yael Rosenberg-HassonDepartment of Immunology, Fairchild Science Building, D033, 299 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5124. Electronic address: Yaelhr@stanford.edu.
Rajiv V AlluriDepartment of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427. Electronic address: rvalluri@stanford.edu.
John S TamaresisDepartment of Biomedical Data Science, Room T101F, Redwood Building, 150 Governor's Lane, Stanford University School of Medicine, Stanford, CA 94305-5405. Electronic address: John.s.tamaresis@stanford.edu.
Michael H BachmannDepartment of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427. Electronic address: mhb@stanford.edu.
Kitty LeeCell Sciences Imaging Facility, Beckman Center (B050B), Stanford University School of Medicine, Stanford, CA 94305-5301. Electronic address: microscopy@stanford.edu.
William J MaloneyDepartment of Orthopaedic Surgery, 450 Broadway Street, Pavillion C, 4th Floor, Stanford University School of Medicine, Redwood City, CA 94063-6342. Electronic address: wmaloney@stanford.edu.
Christopher H ContagDepartment of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427. Electronic address: ccontag@stanford.edu.
Bonnie L KingDepartment of Pediatrics, 150E Clark Center, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5427. Electronic address: bonnie.king@stanford.edu.
Stanford University · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
Dynamic Imaging of EMT in the Breast Cancer MicroenvironmentR01CA172895 · NCI · STANFORD UNIVERSITY · PI GERTLER, FRANK B, SOLGAARD, OLAV · 2013 to 2017
$3.2M
NCI NIH HHS 5R01CA172895-02NCI NIH HHS P30 CA124435NCI NIH HHS P30CA124435NCI NIH HHS R01 CA172895
6 · The paper itself

Abstract

BACKGROUND/

objectivesBone is a preferred site of breast cancer metastasis, suggesting the presence of tissue-specific features that attract and promote the outgrowth of breast cancer cells. We sought to identify parameters of human bone tissue associated with breast cancer cell osteotropism and colonization in the metastatic niche.

methodsMigration and colonization patterns of MDA-MB-231-fLuc-EGFP (luciferase-enhanced green fluorescence protein) and MCF-7-fLuc-EGFP breast cancer cells were studied in co-culture with cancellous bone tissue fragments isolated from 14 hip arthroplasties. Breast cancer cell migration into tissues and toward tissue-conditioned medium was measured in Transwell migration chambers using bioluminescence imaging and analyzed as a function of secreted factors measured by multiplex immunoassay. Patterns of breast cancer cell colonization were evaluated with fluorescence microscopy and immunohistochemistry.

resultsEnhanced MDA-MB-231-fLuc-EGFP breast cancer cell migration to bone-conditioned versus control medium was observed in 12/14 specimens (P = .0014) and correlated significantly with increasing levels of the adipokines/cytokines leptin (P = .006) and IL-1β (P = .001) in univariate and multivariate regression analyses. Fluorescence microscopy and immunohistochemistry of fragments underscored the extreme adiposity of adult human bone tissues and revealed extensive breast cancer cell colonization within the marrow adipose tissue compartment.

conclusionsOur results show that breast cancer cells migrate to human bone tissue-conditioned medium in association with increasing levels of leptin and IL-1β, and colonize the bone marrow adipose tissue compartment of cultured fragments. Bone marrow adipose tissue and its molecular signals may be important but understudied components of the breast cancer metastatic niche.

Indexed as

Cell MovementCell ProliferationAdipocytesAdipose TissueBone and BonesBone MarrowBreast NeoplasmsCell AdhesionCell Line, TumorCellular MicroenvironmentCoculture TechniquesCulture Media, ConditionedFemaleGreen Fluorescent ProteinsHumansImmunohistochemistryCulture Media, ConditionedGreen Fluorescent ProteinsInterleukin-1betaLeptinLuciferases

Identifiers

PMID26696367
PMCPMC4688564
OpenAlexW2193682462

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.