Evidence map›Paper›PMID 25241036›Full record

ArticleNature cell biology2014

ΔNp63 promotes stem cell activity in mammary gland development and basal-like breast cancer by enhancing Fzd7 expression and Wnt signalling.

Rumela Chakrabarti, Yong Wei, Julie Hwang, Xiang Hang, Mario Andres Blanco, Abrar Choudhury, Benjamin Tiede, Rose-Anne Romano, Christina DeCoste, Laura Mercatali and 6 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 143 papers.

0numbers the graph read from it
0cells of the map it votes in
143citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

143 citing papers in PubMed, 210 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. FZD7 expression marks mammary tumor-initiating cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Review
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  9. CXCR4Nature communications · 2025
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83 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

16 authors at 8 institutions in 3 countries.

Rumela ChakrabartiDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Yong WeiDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Julie HwangDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Xiang HangDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Mario Andres Blanco1] Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA [2] Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Abrar ChoudhuryDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Benjamin TiedeDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Rose-Anne RomanoDepartment of Biochemistry, Center of Excellence in Bioinformatics and Life Sciences, State University of New York at Buffalo, Buffalo, New York 14203, USA.
Christina DeCosteDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Laura MercataliOsteoncology and Rare Tumors Center, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, 47014 Meldola, Italy.
Toni IbrahimOsteoncology and Rare Tumors Center, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, 47014 Meldola, Italy.
Dino AmadoriOsteoncology and Rare Tumors Center, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, 47014 Meldola, Italy.
Nagarajan KannanTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia V5Z 1L3, Canada.
Connie J EavesTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia V5Z 1L3, Canada.
Satrajit SinhaDepartment of Biochemistry, Center of Excellence in Bioinformatics and Life Sciences, State University of New York at Buffalo, Buffalo, New York 14203, USA.
Yibin Kang1] Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA [2] Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey 08903, USA.
Princeton University · USIstituti di Ricovero e Cura a Carattere Scientifico · ITBC Cancer Agency · CABuffalo State University · USHarvard University Press · USIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITUniversity at Buffalo, State University of New York · USUniversity of British Columbia · CA

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
Metadherin in Metastasis and Chemoresistance of Breast CancerR01CA134519 · NCI · PRINCETON UNIVERSITY · PI KANG, YIBIN · 2008 to 2012
$1.6M
The Role of miRNAs in Epithelial-Mesenchymal Transition and MetastasisR01CA141062 · NCI · PRINCETON UNIVERSITY · PI KANG, YIBIN · 2010 to 2014
$1.6M
NCI NIH HHS P30 CA072720NCI NIH HHS P30CA072720NCI NIH HHS R01 CA134519NCI NIH HHS R01CA134519NCI NIH HHS R01 CA141062NCI NIH HHS R01CA141062NIGMS NIH HHS T32 GM007388
6 · The paper itself

Abstract

Emerging evidence suggests that cancer is populated and maintained by tumour-initiating cells (TICs) with stem-like properties similar to those of adult tissue stem cells. Despite recent advances, the molecular regulatory mechanisms that may be shared between normal and malignant stem cells remain poorly understood. Here we show that the ΔNp63 isoform of the Trp63 transcription factor promotes normal mammary stem cell (MaSC) activity by increasing the expression of the Wnt receptor Fzd7, thereby enhancing Wnt signalling. Importantly, Fzd7-dependent enhancement of Wnt signalling by ΔNp63 also governs tumour-initiating activity of the basal subtype of breast cancer. These findings establish ΔNp63 as a key regulator of stem cells in both normal and malignant mammary tissues and provide direct evidence that breast cancer TICs and normal MaSCs share common regulatory mechanisms.

Indexed as

Wnt Signaling PathwayAnimalsBlotting, WesternBreast NeoplasmsCell Line, TumorEpithelial CellsFrizzled ReceptorsGene Expression Regulation, NeoplasticGreen Fluorescent ProteinsHumansInterleukin Receptor Common gamma SubunitMammary Glands, AnimalMammary Glands, HumanMice, Inbred C57BLMice, Inbred NODMice, KnockoutFrizzled ReceptorsFZD7 protein, humanGreen Fluorescent ProteinsIl2rg protein, mouseInterleukin Receptor Common gamma SubunitTP63 protein, humanTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID25241036
PMCPMC4183725
OpenAlexW2066446030

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.