Evidence map›Paper›PMID 31123087›Full record

ArticleCancer research2019

Asporin Restricts Mesenchymal Stromal Cell Differentiation, Alters the Tumor Microenvironment, and Drives Metastatic Progression.

Robert M Hughes, Brian W Simons, Hamda Khan, Rebecca Miller, Valentina Kugler, Samantha Torquato, Debebe Theodros, Michael C Haffner, Tamara Lotan, Jessie Huang and 10 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.9field-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

48 citing papers in PubMed, 84 citations in OpenAlex.

  1. Article
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  10. The fibroinflammatory response in cancer.Nature reviews. Cancer · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. ASPORIN: A root of the matter in tumors and their host environment.Biochimica et biophysica acta. Reviews on cancer · 2024
    Review
  16. Review
  17. Article
  18. Review
  19. Article
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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

20 authors at 3 institutions in 2 countries.

Robert M HughesThe James Buchanan Brady Urological Institute, Department of Urology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Brian W SimonsThe James Buchanan Brady Urological Institute, Department of Urology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Hamda KhanThe James Buchanan Brady Urological Institute, Department of Urology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Rebecca MillerThe James Buchanan Brady Urological Institute, Department of Urology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Valentina KuglerThe James Buchanan Brady Urological Institute, Department of Urology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Samantha TorquatoThe James Buchanan Brady Urological Institute, Department of Urology, Johns Hopkins School of Medicine, Baltimore, Maryland.ORCID 0000-0001-6724-0947
Debebe TheodrosThe Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Michael C HaffnerThe Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Tamara LotanThe Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Jessie HuangThe Department of Environmental Health and Engineering, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Elai DavicioniGenome Dx Biosciences, Inc., Vancouver, British Columbia, Canada.ORCID 0000-0001-9136-099X
Steven S AnThe Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Ryan C RiddleThe Department of Orthopedic Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland.
Daniel L J ThorekThe Department of Radiology, Johns Hopkins School of Medicine, Baltimore, Maryland.ORCID 0000-0003-2437-1239
Isla P GarrawayThe Department of Urology, David Geffen School of Medicine at UCLA, Los Angeles, California.
Elana J FertigThe Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland.
John T IsaacsThe James Buchanan Brady Urological Institute, Department of Urology, Johns Hopkins School of Medicine, Baltimore, Maryland.
W Nathaniel BrennenThe Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland.ORCID 0000-0001-9807-7433
Ben H ParkThe Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Paula J HurleyThe James Buchanan Brady Urological Institute, Department of Urology, Johns Hopkins School of Medicine, Baltimore, Maryland. phurley2@jhmi.edu.
Johns Hopkins University · USResearch Canada · CAUniversity of California, Los Angeles · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
Research Resource for Human Organs and Tissues (U42)U42OD011158 · OD · NATIONAL DISEASE RESEARCH INTERCHANGE · PI BELL, THOMAS J · 2012 to 2025
$25.0M
Circulating plasma tumor DNA as a biomarker for early stage breast cancerR01CA194024 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO · 2016 to 2020
$1.9M
Regulation of Metastatic Development by Heritable Variants in the Tumor MicroenvironmentR01CA211695 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HURLEY, PAULA JILL · 2018 to 2023
$1.9M
Kallikrein-Targeted Alpha-Particle Therapy of Late-Stage Prostate CancerR01CA201035 · NCI · WASHINGTON UNIVERSITY · PI THOREK, DANIEL LYNDON JAFFE · 2017 to 2020
$1.4M
Molecular complete response in blood as a predictor for pathologic complete response after neoadjuvant therapy for breast cancerR01CA214494 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO · 2018 to 2023
$1.1M
NCI NIH HHS P30 CA006973NCI NIH HHS R01 CA194024NCI NIH HHS R01 CA201035NCI NIH HHS R01 CA211695NCI NIH HHS R01 CA214494NIH HHS U42 OD011158
6 · The paper itself

Abstract

Tumor progression to metastasis is not cancer cell autonomous, but rather involves the interplay of multiple cell types within the tumor microenvironment. Here we identify asporin (ASPN) as a novel, secreted mesenchymal stromal cell (MSC) factor in the tumor microenvironment that regulates metastatic development. MSCs expressed high levels of ASPN, which decreased following lineage differentiation. ASPN loss impaired MSC self-renewal and promoted terminal cell differentiation. Mechanistically, secreted ASPN bound to BMP-4 and restricted BMP-4-induced MSC differentiation prior to lineage commitment. ASPN expression was distinctly conserved between MSC and cancer-associated fibroblasts (CAF). ASPN expression in the tumor microenvironment broadly impacted multiple cell types. Prostate tumor allografts in ASPN-null mice had a reduced number of tumor-associated MSCs, fewer cancer stem cells, decreased tumor vasculature, and an increased percentage of infiltrating CD8

Indexed as

AnimalsCell DifferentiationCell Line, TumorCell MovementDisease ProgressionExtracellular Matrix ProteinsHEK293 CellsHumansMaleMesenchymal Stem CellsMiceMice, Inbred C57BLNeoplasm MetastasisPC-3 CellsProstatic NeoplasmsTumor MicroenvironmentASPN protein, humanAspn protein, mouseExtracellular Matrix Proteins

Identifiers

PMID31123087
PMCPMC6734938
OpenAlexW2945067244

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.