Evidence map›Paper›PMID 23472872›Full record

ArticleCell stem cell2013

Sox2 cooperates with inflammation-mediated Stat3 activation in the malignant transformation of foregut basal progenitor cells.

Kuancan Liu, Ming Jiang, Yun Lu, Hao Chen, Jun Sun, Shaoping Wu, Wei-Yao Ku, Hiroshi Nakagawa, Yoshiaki Kita, Shoji Natsugoe and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 2 pooled it
10.4field-weighted citation impact, top 1% 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

131 citing papers in PubMed, 2 syntheses or guidelines pooled it, 187 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Esophageal cancer: from pathogenesis to precision therapies.Signal transduction and targeted therapy · 2026
    Review
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  9. Article
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  12. Carcinogenesis trajectories.Frontiers in cell and developmental biology · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Cellular Origins and Lineage Plasticity in Cancer.Cold Spring Harbor perspectives in medicine · 2024
    Review
  18. Article
  19. Article
  20. Article

71 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 3 countries.

Kuancan LiuDepartment of Biomedical Genetics, University of Rochester, Rochester, NY 14642, USA.
Ming Jiang
Yun Lu
Hao Chen
Jun Sun
Shaoping Wu
Wei-Yao Ku
Hiroshi Nakagawa
Yoshiaki Kita
Shoji Natsugoe
Jeffrey H Peters
Anil Rustgi
Mark W Onaitis
Amy Kiernan
Xiaoxin Chen
Jianwen Que
University of Rochester · USKagoshima University · JPNorth Carolina Central University · USRush University Medical Center · USUniversity of Pennsylvania · USDuke University · USTsinghua University · CN

Funding

Transformed Esophageal Epithelial Cells and the Tumor MicroenvironmentP01CA098101 · NCI · UNIVERSITY OF PENNSYLVANIA · PI RUSTGI, ANIL K · 2003 to 2023
$31.7M
Targeting the MEKK2-ERK5 Signaling Node in Triple Negative Breast CancerU54CA156735 · NCI · NORTH CAROLINA CENTRAL UNIVERSITY · PI RICHARDSON, MICHELER RICARDO · 2010 to 2021
$13.0M
Inflammation and the esophageal tumor microenvironmentU01CA143056 · NCI · UNIVERSITY OF PENNSYLVANIA · PI MAHMOOD, UMAR, RUSTGI, ANIL K · 2009 to 2013
$3.1M
The role of transcription factor Sox2 in the homeostasis of the adult esophagusR00DK082650 · NIDDK · UNIVERSITY OF ROCHESTER · PI QUE, JIANWEN · 2012 to 2013
$483k
The Role of transcription factor Sox2 in the homeostasis of the adult esophagusK99DK082650 · NIDDK · UNIVERSITY OF ROCHESTER · PI QUE, JIANWEN · 2010 to 2011
$161k
NCI NIH HHS P01 CA098101NCI NIH HHS P01-CA098101NCI NIH HHS U01 CA143056NCI NIH HHS U01-CA143056NCI NIH HHS U54 CA156735NIDDK NIH HHS K99 DK082650NIDDK NIH HHS K99/R00 DK082650NIDDK NIH HHS R00 DK082650
6 · The paper itself

Abstract

Sox2 regulates the self-renewal of multiple types of stem cells. Recent studies suggest it also plays oncogenic roles in the formation of squamous carcinoma in several organs, including the esophagus where Sox2 is predominantly expressed in the basal progenitor cells of the stratified epithelium. Here, we use mouse genetic models to reveal a mechanism by which Sox2 cooperates with microenvironmental signals to malignantly transform epithelial progenitor cells. Conditional overexpression of Sox2 in basal cells expands the progenitor population in both the esophagus and forestomach. Significantly, carcinoma only develops in the forestomach, where pathological progression correlates with inflammation and nuclear localization of Stat3 in progenitor cells. Importantly, co-overexpression of Sox2 and activated Stat3 (Stat3C) also transforms esophageal basal cells but not the differentiated suprabasal cells. These findings indicate that basal stem/progenitor cells are the cells of origin of squamous carcinoma and that cooperation between Sox2 and microenvironment-activated Stat3 is required for Sox2-driven tumorigenesis.

Indexed as

AnimalsCells, CulturedHumansInflammationMiceSOXB1 Transcription FactorsSTAT3 Transcription FactorStem CellsSOXB1 Transcription FactorsSTAT3 Transcription Factor

Identifiers

PMID23472872
PMCPMC3594795
OpenAlexW2007788183

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.