Evidence map›Paper›PMID 31819067›Full record

ArticleScientific reports2019

Bone secreted factors induce cellular quiescence in prostate cancer cells.

Li-Yuan Yu-Lee, Yu-Chen Lee, Jing Pan, Song-Chang Lin, Tianhong Pan, Guoyu Yu, David H Hawke, Bih-Fang Pan, Sue-Hwa Lin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. A cell cycle centric view of tumour dormancy.British journal of cancer · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review old bone, new tricks.Clinical & experimental metastasis · 2022
    Review
  15. Article
  16. Review
  17. Patterns of indolence in prostate cancer (Review).Experimental and therapeutic medicine · 2022
    Review
  18. Review
  19. The Osteoclast Traces the Route to Bone Tumors and Metastases.Frontiers in cell and developmental biology · 2022
    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

9 authors at 2 institutions in 1 country.

Li-Yuan Yu-LeeDepartment of Medicine, Baylor College of Medicine, Houston, Texas, 77030, United States of America. yulee@bcm.edu.ORCID http://orcid.org/0000-0002-6122-4054
Yu-Chen LeeDepartment of Translational Molecular Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, 77030, United States of America.
Jing PanDepartment of Medicine, Baylor College of Medicine, Houston, Texas, 77030, United States of America.
Song-Chang LinDepartment of Translational Molecular Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, 77030, United States of America.
Tianhong PanDepartment of Orthopedic Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, 77030, United States of America.
Guoyu YuDepartment of Translational Molecular Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, 77030, United States of America.
David H HawkeThe Proteomics and Metabolomics Facility, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, 77030, United States of America.ORCID http://orcid.org/0000-0002-6102-7843
Bih-Fang PanThe Proteomics and Metabolomics Facility, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, 77030, United States of America.
Sue-Hwa LinDepartment of Translational Molecular Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, 77030, United States of America. slin@mdanderson.org.ORCID http://orcid.org/0000-0002-2353-406X
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Targeting Tumor Microenvironment-Induced Therapy Resistance in Prostate Cancer Bone MetastasisP50CA140388 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOGOTHETIS, CHRISTOPHER J., THOMPSON, TIMOTHY CHARLES · 2009 to 2022
$23.4M
Endothelial-to-osteoblast transition in prostate cancer bone metastasisR01CA174798 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, SUE-HWA · 2013 to 2023
$3.0M
Cancer Prevention and Research Institute of Texas (Cancer Prevention Research Institute of Texas) RP150179NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA140388NCI NIH HHS R01 CA174798U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) 5P50 CA140388U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA174798
6 · The paper itself

Abstract

Disseminated tumor cells (DTCs) undergo a dormant state in the distant metastatic site(s) before becoming overt metastatic diseases. In prostate cancer (PCa), bone metastasis can occur years after prostatectomy, suggesting that bone may provide dormancy-inducing factors. To search for these factors, we prepared conditioned media (CM) from calvariae. Using live-cell imaging, we found that Calvarial-CM treatment increased cellular quiescence in C4-2B4 PCa cells. Mass spectrometry analysis of Calvarial-CM identified 132 secreted factors. Western blot and ELISA analyses confirmed the presence of several factors, including DKK3, BMP1, neogenin and vasorin in the Calvarial-CM. qRT-PCR analysis of total calvariae versus isolated osteoblasts showed that DKK3, BMP1, vasorin and neogenin are mainly expressed by osteoblasts, while MIA, LECT1, NGAL and PEDF are expressed by other calvarial cells. Recombinant human DKK3, BMP1, vasorin, neogenin, MIA and NGAL treatment increased cellular quiescence in both C4-2b and C4-2B4 PCa cells. Mechanistically, DKK3, vasorin and neogenin, but not BMP1, increased dormancy through activating the p38MAPK signaling pathway. Consistently, DKK3, vasorin and neogenin failed to induce dormancy in cells expressing dominant-negative p38αMAPK while BMP1 remained active, suggesting that BMP1 uses an alternative dormancy signaling pathway. Thus, bone secretes multiple dormancy-inducing factors that employ distinct signaling pathways to induce DTC dormancy in bone.

Indexed as

Adaptor Proteins, Signal TransducingBone Morphogenetic Protein 1Bone NeoplasmsCell Line, TumorCulture Media, ConditionedGene Expression Regulation, NeoplasticHumansMaleMembrane ProteinsNeoplasm MetastasisOsteoblastsp38 Mitogen-Activated Protein KinasesProstateProstatectomyProstatic NeoplasmsSignal TransductionAdaptor Proteins, Signal TransducingBMP1 protein, humanBone Morphogenetic Protein 1Culture Media, ConditionedDKK3 protein, humanMembrane Proteinsneogeninp38 Mitogen-Activated Protein Kinases

Identifiers

PMID31819067
PMCPMC6901558
OpenAlexW2991843036

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.