Evidence map›Paper›PMID 30520817›Full record

ArticleThe American journal of surgical pathology2019

The HTN3-MSANTD3 Fusion Gene Defines a Subset of Acinic Cell Carcinoma of the Salivary Gland.

Simon Andreasen, Sushama Varma, Nicholas Barasch, Lester D R Thompson, Markku Miettinen, Lisa Rooper, Edward B Stelow, Tina K Agander, Raja R Seethala, Simion I Chiosea and 10 more

Open access · greenAbstract read
In one paragraph

Article in The American journal of surgical pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
7.8field-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

24 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Oncocytic salivary gland carcinomas.Histology and histopathology · 2026
    Review
  3. Review
  4. Review
  5. Article
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  7. Article
  8. Review
  9. NR4A3 Expression Is Consistently Absent in Acinic Cell Carcinomas of the Breast: A Potential Nosologic Shift.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2023
    Article
  10. Review
  11. The evolving role of molecular pathology in the diagnosis of salivary gland tumours with potential pitfalls.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2022
    Review
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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

20 authors at 10 institutions in 2 countries.

Simon AndreasenDepartment of Otorhinolaryngology Head & Neck Surgery and Audiology, Rigshospitalet, Copenhagen University Hospital.
Sushama VarmaDepartment of Pathology, Stanford University School of Medicine, Stanford, CA.
Nicholas BaraschDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Lester D R ThompsonSouthern California Permanente Medical Group, Woodland Hills, CA.
Markku MiettinenLaboratory of Pathology, NCI/NIH, Bethesda.
Lisa RooperDepartment of Pathology, The Johns Hopkins Medical Institutions, Baltimore, MD.
Edward B StelowDepartment of Pathology, The University of Virginia, Charlottesville, VA.
Tina K AganderDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen.
Raja R SeethalaDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Simion I ChioseaDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Preben HomøeDepartment of Otorhinolaryngology and Maxillofacial Surgery, Zealand University Hospital, Køge.
Irene WesselDepartment of Otorhinolaryngology Head & Neck Surgery and Audiology, Rigshospitalet, Copenhagen University Hospital.
Stine R LarsenDepartment of Pathology, Odense University Hospital, Odense.
Daiva ErentaiteDepartment of Pathology, Aalborg University Hospital, Aalborg.
Justin A BishopDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX.
Benedicte P UlhøiDepartment of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Katalin KissDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen.
Linea C MelchiorDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen.
Jonathan R PollackDepartment of Pathology, Stanford University School of Medicine, Stanford, CA.
Robert B WestDepartment of Pathology, Stanford University School of Medicine, Stanford, CA.
Copenhagen University Hospital · DKStanford University · USUniversity of Pittsburgh Medical Center · USRigshospitalet · DKWoodland Hills Medical Center · USZealand University Hospital Køge · DKAalborg University Hospital · DKNational Institutes of Health · USThe University of Texas Southwestern Medical Center · USUniversity of Virginia · US

Funding

Immunohistochemical and genomic analysis of tumorsZIABC011427 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MIETTINEN, MARKKU · 2012 to 2025
$24.0M
Intramural NIH HHS ZIA BC011427
6 · The paper itself

Abstract

The spectrum of tumors arising in the salivary glands is wide and has recently been shown to harbor a network of tumor-specific fusion genes. Acinic cell carcinoma (AciCC) is one of the more frequently encountered types of salivary gland carcinoma, but it has remained a genetic orphan until recently when a fusion between the HTN3 and MSANTD3 genes was described in one case. Neither of these 2 genes is known to be implicated in any other malignancy. This study was undertaken to investigate whether the HTN3-MSANTD3 fusion is a recurrent genetic event in AciCC and whether it is a characteristic of one of its histological variants. Of the 273 AciCCs screened, 9 cases showed rearrangement of MSANTD3 by break-apart fluorescence in situ hybridization, 2 had 1 to 2 extra signals, and 1 had gain, giving a total of 4.4% with MSANTD3 aberrations. In 6 of 7 available cases with MSANTD3 rearrangement, the HTN3-MSANTD3 fusion transcript was demonstrated with real-time polymerase chain reaction. Histologically, all fusion-positive cases were predominantly composed of serous tumor cells growing in solid sheets, with serous tumor cells expressing DOG-1 and the intercalated duct-like cell component being CK7 positive and S-100 positive in 6/9 cases. All but one case arose in the parotid gland, and none of the patients experienced a recurrence during follow-up. In contrast, the case with MSANTD3 gain metastasized to the cervical lymph nodes and lungs. In conclusion, we find the HTN3-MSANTD3 gene fusion to be a recurrent event in AciCC with prominent serous differentiation and an indolent clinical course.

Indexed as

Oncogene FusionAdultAgedCarcinoma, Acinar CellDNA-Binding ProteinsFemaleHistatinsHumansMaleMiddle AgedSalivary Gland NeoplasmsDNA-Binding ProteinsHistatinsHTN3 protein, humanMSANTD3 protein, human

Identifiers

PMID30520817
PMCPMC8191383
OpenAlexW2904510099

What OpenQuestion holds

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Registered trials

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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.