Evidence map›Paper›PMID 32103065›Full record

ArticleScientific reports2020

Cell surface GRP78 promotes stemness in normal and neoplastic cells.

Clay Conner, Tyson W Lager, Ian H Guldner, Min-Zu Wu, Yuriko Hishida, Tomoaki Hishida, Sergio Ruiz, Amanda E Yamasaki, Robert C Gilson, Juan Carlos Izpisua Belmonte and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
6.3field-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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 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

14 authors at 6 institutions in 2 countries.

Clay ConnerDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA.
Tyson W LagerDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA.
Ian H GuldnerDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA.
Min-Zu WuDepartment of Inflammation, Amgen, Thousand Oaks, CA, 91320, USA.
Yuriko HishidaGene Expression Laboratory, The Salk Institute for Biological Sciences, La Jolla, CA, 92037, USA.
Tomoaki HishidaGene Expression Laboratory, The Salk Institute for Biological Sciences, La Jolla, CA, 92037, USA.
Sergio RuizLaboratory of Genome Integrity, National Cancer Institute, Bethesda, MD, 20814, USA.
Amanda E YamasakiDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA.
Robert C GilsonDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA.
Juan Carlos Izpisua BelmonteGene Expression Laboratory, The Salk Institute for Biological Sciences, La Jolla, CA, 92037, USA.ORCID http://orcid.org/0000-0003-0557-8875
Peter C GrayBiotheranostics, Inc., San Diego, CA, 92121, USA.
Jonathan A KelberDepartment of Biology, California State University Northridge, Northridge, CA, 91330, USA.
Siyuan ZhangDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA.ORCID http://orcid.org/0000-0003-0910-3666
Athanasia D PanopoulosDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA. apanopou@nd.edu.
University of Notre Dame · USSalk Institute for Biological Studies · USAmgen (United States) · USCalifornia State University, Northridge · USNational Cancer Institute · USTheranostics (New Zealand) · NZ

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
SPATIOTEMPORAL MECHANISMS OF EIF5A1/2-MEDIATED METASTASIS IN TRIPLE-NEGATIVE BREAST CANCERSC1GM121182 · NIGMS · CALIFORNIA STATE UNIVERSITY NORTHRIDGE · PI KELBER, JONATHAN · 2017 to 2024
$3.2M
Molecular Determinants of TotipotencyZIABC011813 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RUIZ, SERGIO · 2018 to 2025
$3.0M
Role of ETS-Transcription Factors in Regulating Cell FateZIABC011808 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RUIZ, SERGIO · 2018 to 2025
$2.7M
Identification of molecular pathways regulating quiescence in pluripotent cellsZIABC011809 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RUIZ, SERGIO · 2018 to 2025
$2.1M
Indiana Clinical and Translational Sciences InstituteTL1TR001107 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$2.0M
Scripps Translational Science Institute (KL2)KL2TR000110 · NCATS · SCRIPPS RESEARCH INSTITUTE, THE · PI TOPOL, ERIC JEFFREY · 2012 to 2013
$896k
NCATS NIH HHS KL2 TR000110NCATS NIH HHS TL1 TR001107
6 · The paper itself

Abstract

Reliable approaches to identify stem cell mechanisms that mediate aggressive cancer could have great therapeutic value, based on the growing evidence of embryonic signatures in metastatic cancers. However, how to best identify and target stem-like mechanisms aberrantly acquired by cancer cells has been challenging. We harnessed the power of reprogramming to examine GRP78, a chaperone protein generally restricted to the endoplasmic reticulum in normal tissues, but which is expressed on the cell surface of human embryonic stem cells and many cancer types. We have discovered that (1) cell surface GRP78 (sGRP78) is expressed on iPSCs and is important in reprogramming, (2) sGRP78 promotes cellular functions in both pluripotent and breast cancer cells (3) overexpression of GRP78 in breast cancer cells leads to an induction of a CD24

Indexed as

Cell DifferentiationCell Self RenewalAnimalsBreast NeoplasmsCell Line, TumorCell Transformation, NeoplasticCellular ReprogrammingEndoplasmic Reticulum Chaperone BiPFemaleHeat-Shock ProteinsHEK293 CellsHumansInduced Pluripotent Stem CellsLung NeoplasmsMiceMice, KnockoutEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsHSPA5 protein, humanHspa5 protein, mouseRNA, Small InterferingTranscription Factors

Identifiers

PMID32103065
PMCPMC7044190
OpenAlexW3007771222

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.