Evidence map›Paper›PMID 30065048›Full record

ArticleCancer research2018

Modulating Bone Marrow Hematopoietic Lineage Potential to Prevent Bone Metastasis in Breast Cancer.

Jessalyn M Ubellacker, Ninib Baryawno, Nicolas Severe, Molly J DeCristo, Jaclyn Sceneay, John N Hutchinson, Marie-Therese Haider, Catherine S Rhee, Yuanbo Qin, Walter M Gregory and 6 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Increased blood CSF3RAmerican journal of cancer research · 2024
    Article
  5. Review
  6. Aging · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Metastasis as a systemic disease: molecular insights and clinical implications.Biochimica et biophysica acta. Reviews on cancer · 2019
    Review
  16. Review
  17. Article
  18. 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

16 authors at 7 institutions in 2 countries.

Jessalyn M UbellackerHematology Division, Brigham & Women's Hospital, Boston, Massachusetts.
Ninib BaryawnoDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts.
Nicolas SevereDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts.
Molly J DeCristoHematology Division, Brigham & Women's Hospital, Boston, Massachusetts.
Jaclyn SceneayHematology Division, Brigham & Women's Hospital, Boston, Massachusetts.
John N HutchinsonDepartment of Biostatistics, Harvard T.H. Chan, School of Public Health, Boston, Massachusetts.ORCID 0000-0002-7804-7576
Marie-Therese HaiderAcademic Unit of Clinical Oncology, Department of Oncology & Metabolism, Weston Park Hospital, University of Sheffield, Sheffield, United Kingdom.
Catherine S RheeDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts.
Yuanbo QinHematology Division, Brigham & Women's Hospital, Boston, Massachusetts.
Walter M GregoryClinical Trials Research Unit, University of Leeds, Leeds, United Kingdom.ORCID 0000-0003-2641-8416
Ana C Garrido-CastroDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-5989-6636
Ingunn HolenAcademic Unit of Clinical Oncology, Department of Oncology & Metabolism, Weston Park Hospital, University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0002-8759-6913
Janet E BrownAcademic Unit of Clinical Oncology, Department of Oncology & Metabolism, Weston Park Hospital, University of Sheffield, Sheffield, United Kingdom.
Robert E ColemanAcademic Unit of Clinical Oncology, Department of Oncology & Metabolism, Weston Park Hospital, University of Sheffield, Sheffield, United Kingdom.
David T ScaddenDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts.
Sandra S McAllisterHematology Division, Brigham & Women's Hospital, Boston, Massachusetts. smcallister1@bwh.harvard.edu.
Brigham and Women's Hospital · USWeston Park Cancer Centre · GBCenter for Cancer Research · USBroad Institute · USDana-Farber Cancer Institute · USHarvard University · USLeeds Trinity University · GB

Funding

Harvard Clinical and Translational Science CenterUL1TR001102 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2013 to 2017
$106.2M
Molecular, Cellular, & Developmental Dynamics PhD ProgramT32GM007226 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI VAN VACTOR, DAVID L. · 1985 to 2021
$14.4M
Stromal Regulation of Bone MetastasisU54CA163191 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KALLURI, RAGHU · 2011 to 2015
$4.8M
Understanding How Breast Cancers Activate and Respond to the Systemic EnvironmentR01CA166284 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI MCALLISTER, SANDRA S · 2012 to 2018
$2.2M
Deconvoluting the hematopoietic niche under stressR01DK107784 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI KHARCHENKO, PETER V, SCADDEN, DAVID T · 2016 to 2019
$2.1M
Elucidating the role of bisphosphonates in the inhibition of breast cancerF31CA195797 · NCI · HARVARD MEDICAL SCHOOL · PI UBELLACKER, JESSALYN · 2016 to 2017
$65k
NCATS NIH HHS UL1 TR001102NCI NIH HHS F31 CA195797NCI NIH HHS R01 CA166284NCI NIH HHS U54 CA163191NIDDK NIH HHS R01 DK107784NIGMS NIH HHS T32 GM007226
6 · The paper itself

Abstract

The presence of disseminated tumor cells in breast cancer patient bone marrow aspirates predicts decreased recurrence-free survival. Although it is appreciated that physiologic, pathologic, and therapeutic conditions impact hematopoiesis, it remains unclear whether targeting hematopoiesis presents opportunities for limiting bone metastasis. Using preclinical breast cancer models, we discovered that marrow from mice treated with the bisphosphonate zoledronic acid (ZA) are metastasis-suppressive. Specifically, ZA modulated hematopoietic myeloid/osteoclast progenitor cell (M/OCP) lineage potential to activate metastasis-suppressive activity. Granulocyte-colony stimulating factor (G-CSF) promoted ZA resistance by redirecting M/OCP differentiation. We identified M/OCP and bone marrow transcriptional programs associated with metastasis suppression and ZA resistance. Analysis of patient blood samples taken at randomization revealed that women with high-plasma G-CSF experienced significantly worse outcome with adjuvant ZA than those with lower G-CSF levels. Our findings support discovery of therapeutic strategies to direct M/OCP lineage potential and biomarkers that stratify responses in patients at risk of recurrence.

Indexed as

Cell LineageAnimalsAntineoplastic AgentsBiomarkersBone MarrowBone Marrow CellsBone NeoplasmsBreast NeoplasmsCell DifferentiationCell Line, TumorFemaleGranulocyte Colony-Stimulating FactorHematopoiesisHematopoietic Stem CellsHumansMacrophagesAntineoplastic AgentsBiomarkersGranulocyte Colony-Stimulating FactorZoledronic Acid

Identifiers

PMID30065048
PMCPMC6309204
OpenAlexW2885050929

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.