Evidence map›Paper›PMID 30622340›Full record

ArticleOncogene2019

A Sox2-Sox9 signalling axis maintains human breast luminal progenitor and breast cancer stem cells.

Giacomo Domenici, Iskander Aurrekoetxea-Rodríguez, Bruno M Simões, Miriam Rábano, So Young Lee, Julia San Millán, Valentine Comaills, Erik Oliemuller, José A López-Ruiz, Ignacio Zabalza and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
10.1field-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

99 citing papers in PubMed, 155 citations in OpenAlex.

  1. Article
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  9. Review
  10. Article
  11. SOX9: an important factor in regulating breast cancer.European journal of medical research · 2025
    Review
  12. A spatially organizedScience advances · 2025
    Article
  13. Article
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39 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 2 countries.

Giacomo DomeniciCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain.
Iskander Aurrekoetxea-RodríguezCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain.
Bruno M SimõesCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain.ORCID http://orcid.org/0000-0003-1253-6657
Miriam RábanoCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain.
So Young LeeCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain.
Julia San MillánCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain.
Valentine ComaillsCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain.ORCID http://orcid.org/0000-0001-8857-6976
Erik OliemullerThe Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK.
José A López-RuizRadiodiagnostic Service PreteImagen, Bilbao, Spain.
Ignacio ZabalzaDepartment of Pathology, Galdakao-Usansolo Hospital, Galdakao, Spain.
Beatrice A HowardThe Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK.ORCID http://orcid.org/0000-0002-9162-0314
Robert M KyptaCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain.
Maria dM VivancoCIC bioGUNE, Technological Park Bizkaia, Derio, 48160, Spain. mdmvivanco@cicbiogune.es.
CIC bioGUNE · ESInstitute of Cancer Research · GBHospital de Galdakao · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased cancer stem cell content during development of resistance to tamoxifen in breast cancer is driven by multiple signals, including Sox2-dependent activation of Wnt signalling. Here, we show that Sox2 increases and estrogen reduces the expression of the transcription factor Sox9. Gain and loss of function assays indicate that Sox9 is implicated in the maintenance of human breast luminal progenitor cells. CRISPR/Cas knockout of Sox9 reduces growth of tamoxifen-resistant breast tumours in vivo. Mechanistically, Sox9 acts downstream of Sox2 to control luminal progenitor cell content and is required for expression of the cancer stem cell marker ALDH1A3 and Wnt signalling activity. Sox9 is elevated in breast cancer patients after endocrine therapy failure. This new regulatory axis highlights the relevance of SOX family transcription factors as potential therapeutic targets in breast cancer.

Indexed as

Drug Resistance, NeoplasmBreastBreast NeoplasmsCell LineCell ProliferationEpithelial CellsEstrogensFemaleGene Expression Regulation, NeoplasticHumansMCF-7 CellsNeoplastic Stem CellsSignal TransductionSOX9 Transcription FactorSOXB1 Transcription FactorsTamoxifenEstrogensSOX2 protein, humanSOX9 protein, humanSOX9 Transcription FactorSOXB1 Transcription FactorsTamoxifen

Identifiers

PMID30622340
PMCPMC6756022
OpenAlexW2910068212

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.