Evidence map›Paper›PMID 31226820›Full record

ArticleCells2019

Fibronectin Regulation of Integrin B1 and SLUG in Circulating Tumor Cells.

Jeannette Huaman, Michelle Naidoo, Xingxing Zang, Olorunseun O Ogunwobi

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Jeannette HuamanDepartment of Biological Sciences, Hunter College of The City University of New York, New York, NY 10065, USA. JHUAMAN@genectr.hunter.cuny.edu.
Michelle NaidooDepartment of Biological Sciences, Hunter College of The City University of New York, New York, NY 10065, USA. michelle.naidoo86@myhunter.cuny.edu.
Xingxing ZangDepartments of Microbiology and Immunology, and Medicine (Oncology), Albert Einstein College of Medicine, Bronx, NY 10461, USA. xingxing.zang@einstein.yu.edu.
Olorunseun O OgunwobiDepartment of Biological Sciences, Hunter College of The City University of New York, New York, NY 10065, USA. ogunwobi@genectr.hunter.cuny.edu.ORCID 0000-0003-3388-2137
The Graduate Center, CUNY · USAlbert Einstein College of Medicine · US

Funding

RISE Program Hunter College Option IIIR25GM060665 · NIGMS · HUNTER COLLEGE · PI ORTIZ, BENJAMIN D.,, SERRANO, PETER A · 2000 to 2022
$22.8M
TUFCCC/HC Regional Comprehensive Cancer Health PartnershipU54CA221705 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI Yin Tan · 2018 to 2026
$16.3M
TUFCCC/HC Regional Comprehensive Cancer Health PartnershipU54CA221704 · NCI · HUNTER COLLEGE · PI Joel Erblich, Jennifer S Ford · 2018 to 2026
$10.6M
NCI NIH HHS U54 CA221704NCI NIH HHS U54 CA221705NIGMS NIH HHS R25 GM060665
6 · The paper itself

Abstract

Metastasis is the leading cause of cancer death worldwide. Circulating tumor cells (CTCs) are a critical step in the metastatic cascade and a good tool to study this process. We isolated CTCs from a syngeneic mouse model of hepatocellular carcinoma (HCC) and a human xenograft mouse model of castration-resistant prostate cancer (CRPC). From these models, novel primary tumor and CTC cell lines were established. CTCs exhibited greater migration than primary tumor-derived cells, as well as epithelial-to-mesenchymal transition (EMT), as observed from decreased E-cadherin and increased SLUG and fibronectin expression. Additionally, when fibronectin was knocked down in CTCs, integrin B1 and SLUG were decreased, indicating regulation of these molecules by fibronectin. Investigation of cell surface molecules and secreted cytokines conferring immunomodulatory advantage to CTCs revealed decreased major histocompatibility complex class I (MHCI) expression and decreased endostatin, C-X-C motif chemokine 5 (CXCL5), and proliferin secretion by CTCs. Taken together, these findings indicate that CTCs exhibit distinct characteristics from primary tumor-derived cells. Furthermore, CTCs demonstrate enhanced migration in part through fibronectin regulation of integrin B1 and SLUG. Further study of CTC biology will likely uncover additional important mechanisms of cancer metastasis.

Indexed as

AnimalsBiomarkers, TumorCadherinsCarcinoma, HepatocellularCell Line, TumorCell MembraneCell MovementEndostatinsEpithelial-Mesenchymal TransitionFibronectinsHistocompatibility Antigens Class IHumansImmunomodulationIntegrin beta1Liver NeoplasmsMaleBiomarkers, TumorCadherinsEndostatinsFibronectinsHistocompatibility Antigens Class IIntegrin beta1Neoplasm ProteinsSnail Family Transcription Factorscastration resistant prostate cancer (CRPC)circulating tumor cells (CTCs)epithelial-to-mesenchymal transition (EMT)fibronectinhepatocellular carcinoma (HCC)immunomodulationintegrin B1major histocompatibility complex class I (MHCI)metastasisSLUG

Identifiers

PMID31226820
PMCPMC6627780
OpenAlexW2949123839

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.