Evidence map›Paper›PMID 31636389›Full record

ArticleOncogene2020

PREX1 drives spontaneous bone dissemination of ER+ breast cancer cells.

Miranda E Clements, Rachelle W Johnson

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2020. 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
1.1field-weighted citation impact, top 20% 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, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Effects of NaCell biochemistry and biophysics · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Silencing Rac1 and Prex1 Inhibit Epithelial-Mesenchymal Transition in Human Gastric Cancer Cells Induced by Transforming Growth Factor-β1.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  12. gp130 Cytokines Activate Novel Signaling Pathways and Alter Bone Dissemination in ER+ Breast Cancer Cells.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. PtdIns(3,4,5)PProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  18. Frontiers in cell and developmental biology · 2020
    Review
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

2 authors at 1 institution in 1 country.

Miranda E ClementsProgram in Cancer Biology, Vanderbilt University, Nashville, TN, 37232, USA.
Rachelle W JohnsonProgram in Cancer Biology, Vanderbilt University, Nashville, TN, 37232, USA. rachelle.johnson@vumc.org.ORCID http://orcid.org/0000-0003-2755-9851
Vanderbilt University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
CHARACTERIZATION OF BREAST CANCER DORMANCY IN BONER00CA194198 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JOHNSON, RACHELLE W · 2016 to 2018
$747k
NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA068485NCI NIH HHS R00 CA194198NIDDK NIH HHS P30 DK058404
6 · The paper itself

Abstract

A significant proportion of breast cancer patients develop bone metastases, but the mechanisms regulating tumor cell dissemination from the primary site to the skeleton remain largely unknown. Using a novel model of spontaneous bone metastasis derived from human ER+ MCF7 cells, molecular profiling revealed increased PREX1 expression in a cell line established from bone-disseminated MCF7 cells (MCF7b), which were more migratory, invasive, and adhesive in vitro compared with parental MCF7 cells, and this phenotype was mediated by PREX1. MCF7b cells grew poorly in the primary tumor site when reinoculated in vivo, suggesting that these cells are primed to grow in the bone, and were enriched in skeletal sites of metastasis over soft tissue sites. Skeletal dissemination from the primary tumor was reversed with PREX1 knockdown, indicating that PREX1 is a key driver of spontaneous dissemination of tumor cells from the primary site to the bone marrow. In breast cancer patients, PREX1 levels are significantly increased in ER+ tumors and associated with invasive disease and distant metastasis. Together, these findings implicate PREX1 in spontaneous bone dissemination and provide a significant advance to the molecular mechanisms by which breast cancer cells disseminate from the primary tumor site to bone.

Indexed as

AnimalsApoptosisBiomarkers, TumorBone NeoplasmsBreast NeoplasmsCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticGuanine Nucleotide Exchange FactorsHumansMiceMice, NudeReceptors, EstrogenTumor Cells, CulturedXenograft Model Antitumor AssaysBiomarkers, TumorGuanine Nucleotide Exchange FactorsPREX1 protein, humanReceptors, Estrogen

Identifiers

PMID31636389
PMCPMC7007387
OpenAlexW2980696478

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.