Evidence map›Paper›PMID 30515788›Full record

ReviewJournal of cellular physiology2019

RUNX1-dependent mechanisms in biological control and dysregulation in cancer.

Deli Hong, Andrew J Fritz, Jonathan A Gordon, Coralee E Tye, Joseph R Boyd, Kirsten M Tracy, Seth E Frietze, Frances E Carr, Jeffrey A Nickerson, Andre J Van Wijnen and 5 more

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cellular physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Prevalence ofWorld journal of experimental medicine · 2025
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  20. Beyond PathogenicCancers · 2022
    Review
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

15 authors at 4 institutions in 1 country.

Deli HongDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts.
Andrew J FritzDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.ORCID 0000-0002-2220-9943
Jonathan A GordonDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.
Coralee E TyeDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.
Joseph R BoydDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.
Kirsten M TracyDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.ORCID 0000-0003-0985-9447
Seth E FrietzeDepartment of Biomedical and Health Sciences, University of Vermont, Burlington, Vermont.
Frances E CarrDepartment of Pharmacology, University of Vermont, Burlington, Vermont.
Jeffrey A NickersonDepartment of Pediatrics, UMass Medical School, Worcester, Massachusetts.
Andre J Van WijnenDepartments of Orthopedic Surgery and Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-4458-0946
Anthony N ImbalzanoGraduate Program in Cell Biology and Department of Biochemistry and Molecular Pharmacology, UMass Medical School, Worcester, Massachusetts.
Sayyed K ZaidiDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.
Jane B LianDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.
Janet L SteinDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.
Gary S SteinDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.ORCID 0000-0001-8762-5422
University of Vermont · USUniversity of Massachusetts Chan Medical School · USDana-Farber Cancer Institute · USMayo Clinic · US

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI Susan L SANTANGELO · 2017 to 2026
$51.6M
SUBNUCLEAR TARGETING OF TRANSCRIPTION FACTORSP01CA082834 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STEIN, GARY S., STEIN, JANET L · 2001 to 2015
$18.4M
VERMONT IMMUNOBIOLOIGY/ INFECTIOUS DISEASES CENTERP20RR021905 · NCRR · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HILL, JACK · 2006 to 2011
$14.5M
Vermont Immunology/Infectious Diseases CenterP30GM118228 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BUDD, RALPH C · 2016 to 2021
$6.8M
Vermont Breast Cancer Molecular Characterization LaboratoryU01CA196383 · NCI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI SPRAGUE, BRIAN L, STEIN, JANET L · 2015 to 2020
$5.4M
Synthesis of Osteocalcin in BoneR37DE012528 · NIDCR · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIAN, JANE B. · 2008 to 2017
$5.0M
Cell Cycle Regulation of Histone Gene ExpressionR01CA139322 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STEIN, GARY S. · 2009 to 2013
$1.6M
Synthesis of Osteocalcin in BoneR56DE012528 · NIDCR · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI LIAN, JANE B., STEIN, GARY S. · 2018 to 2018
$427k
Supplement to AWD32581 - Fritz fellowship F32CA220935F32CA220935 · NCI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI FRITZ, ANDREW J · 2018 to 2021
$216k
NCI NIH HHS F32 CA220935NCI NIH HHS P01 CA082834NCI NIH HHS R01 CA139322NCI NIH HHS U01 CA196383NCRR NIH HHS P20 RR021905NIDCR NIH HHS R37 DE012528NIDCR NIH HHS R56 DE012528NIGMS NIH HHS P30 GM118228NIGMS NIH HHS U54 GM115516
6 · The paper itself

Abstract

The RUNX1 transcription factor has recently been shown to be obligatory for normal development. RUNX1 controls the expression of genes essential for proper development in many cell lineages and tissues including blood, bone, cartilage, hair follicles, and mammary glands. Compromised RUNX1 regulation is associated with many cancers. In this review, we highlight evidence for RUNX1 control in both invertebrate and mammalian development and recent novel findings of perturbed RUNX1 control in breast cancer that has implications for other solid tumors. As RUNX1 is essential for definitive hematopoiesis, RUNX1 mutations in hematopoietic lineage cells have been implicated in the etiology of several leukemias. Studies of solid tumors have revealed a context-dependent function for RUNX1 either as an oncogene or a tumor suppressor. These RUNX1 functions have been reported for breast, prostate, lung, and skin cancers that are related to cancer subtypes and different stages of tumor development. Growing evidence suggests that RUNX1 suppresses aggressiveness in most breast cancer subtypes particularly in the early stage of tumorigenesis. Several studies have identified RUNX1 suppression of the breast cancer epithelial-to-mesenchymal transition. Most recently, RUNX1 repression of cancer stem cells and tumorsphere formation was reported for breast cancer. It is anticipated that these new discoveries of the context-dependent diversity of RUNX1 functions will lead to innovative therapeutic strategies for the intervention of cancer and other abnormalities of normal tissues.

Indexed as

AnimalsCore Binding Factor Alpha 2 SubunitGene Expression Regulation, NeoplasticHumansMutationNeoplasmsPrognosisSignal TransductionCore Binding Factor Alpha 2 SubunitRUNX1 protein, humanbreast cancercancerhematopoiesisleukemiamammary gland developmentRUNX1

Identifiers

PMID30515788
PMCPMC6395522
OpenAlexW2903256487

What OpenQuestion holds

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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.