Evidence map›Paper›PMID 33451979›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

HAND1 and BARX1 Act as Transcriptional and Anatomic Determinants of Malignancy in Gastrointestinal Stromal Tumor.

Matthew L Hemming, Shannon Coy, Jia-Ren Lin, Jessica L Andersen, Joanna Przybyl, Emanuele Mazzola, Amr H Abdelhamid Ahmed, Matt van de Rijn, Peter K Sorger, Scott A Armstrong and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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

12 authors at 4 institutions in 1 country.

Matthew L HemmingDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts. mhemming@partners.org ssantagata@bics.bwh.harvard.edu.ORCID 0000-0003-4674-7778
Shannon CoyDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-0033-9031
Jia-Ren LinDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-4702-7705
Jessica L AndersenSarcoma Center, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Joanna PrzybylStanford University, Stanford, California.
Emanuele MazzolaDepartment of Data Science, Dana-Farber Cancer Institute and Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Amr H Abdelhamid AhmedDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.
Matt van de RijnStanford University, Stanford, California.
Peter K SorgerDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-3364-1838
Scott A ArmstrongDepartment of Pediatric Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.
George D DemetriDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-0045-4809
Sandro SantagataDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts. mhemming@partners.org ssantagata@bics.bwh.harvard.edu.ORCID 0000-0002-7528-9668
Dana-Farber Cancer Institute · USHarvard University · USBrigham and Women's Hospital · USStanford University · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI A. Heather Eliassen · 1985 to 2026
$330.6M
The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
TRAINING GRANT IN GENETICST32GM007748 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI Anne O'Donnell-Luria, Louise Wilkins-Haug · 1985 to 2026
$12.0M
Systems Pharmacology of Therapeutic and Adverse Responses to ImmuneCheckpoint and Small Molecule DrugsU54CA225088 · NCI · HARVARD MEDICAL SCHOOL · PI SORGER, PETER KARL · 2018 to 2022
$10.8M
Defining clinically relevant transcriptional networks in gastrointestinal stromal tumorK08CA245235 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HEMMING, MATTHEW · 2020 to 2024
$1.2M
NCATS NIH HHS UL1 TR002541NCI NIH HHS K08 CA245235NCI NIH HHS P30 CA006516NCI NIH HHS U54 CA225088NIGMS NIH HHS T32 GM007748
6 · The paper itself

Abstract

purposeGastrointestinal stromal tumor (GIST) arises from interstitial cells of Cajal (ICC) or their precursors, which are present throughout the gastrointestinal tract. Although gastric GIST is commonly indolent and small intestine GIST more aggressive, a molecular understanding of disease behavior would inform therapy decisions in GIST. Although a core transcription factor (TF) network is conserved across GIST, accessory TFs HAND1 and BARX1 are expressed in a disease state-specific pattern. Here, we characterize two divergent transcriptional programs maintained by HAND1 and BARX1, and evaluate their association with clinical outcomes. EXPERIMENTAL

designWe evaluated RNA sequencing and TF chromatin immunoprecipitation with sequencing in GIST samples and cultured cells for transcriptional programs associated with HAND1 and BARX1. Multiplexed tissue-based cyclic immunofluorescence and IHC evaluated tissue- and cell-level expression of TFs and their association with clinical factors.

resultsWe show that HAND1 is expressed in aggressive GIST, modulating

conclusionsOur results define anatomic and transcriptional determinants of GIST and molecular origins of clinical phenotypes. Assessment of HAND1 and BARX1 expression in GIST may provide prognostic information and improve clinical decisions on the administration of adjuvant therapy.

Indexed as

TranscriptomeBasic Helix-Loop-Helix ProteinsBiomarkers, TumorFollow-Up StudiesGastrointestinal NeoplasmsGastrointestinal Stromal TumorsGene Expression Regulation, NeoplasticHomeodomain ProteinsHumansPrognosisRNA-SeqSurvival RateTranscription FactorsTumor Cells, CulturedBARX1 protein, humanBasic Helix-Loop-Helix ProteinsBiomarkers, Tumorhelix-loop-helix protein, eHANDHomeodomain ProteinsTranscription Factors

Identifiers

PMID33451979
PMCPMC7956056
OpenAlexW3120281284

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.