Evidence map›Paper›PMID 32141887›Full record

ArticleThe American journal of surgical pathology2020

A Novel SS18-SSX Fusion-specific Antibody for the Diagnosis of Synovial Sarcoma.

Esther Baranov, Matthew J McBride, Andrew M Bellizzi, Azra H Ligon, Christopher D M Fletcher, Cigall Kadoch, Jason L Hornick

Open access · greenAbstract read
In one paragraph

Article in The American journal of surgical pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
17.1field-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

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 232 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Synovial Sarcoma: Molecular Biology, Pathology, and Therapeutic Strategies.International journal of molecular sciences · 2026
    Review
  5. Article
  6. Solitary fibrous tumor: an updated review.Journal of pathology and translational medicine · 2026
    Article
  7. BRAFOncology research · 2026
    Review
  8. Article
  9. Clinicopathologic and Molecular Genetic Features of Spindle Cell Rhabdomyosarcoma Harboring ZFP64::NCOA2/3 Fusions: A Series of 14 Cases.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2025
    Article
  10. Review
  11. Article
  12. A 23-year-old woman with a headache and imbalance.Brain pathology (Zurich, Switzerland) · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Spindle lesions in the thyroid: a cytological and histological review.Virchows Archiv : an international journal of pathology · 2025
    Review
  18. Article
  19. Article
  20. Identification of a novelTherapeutic advances in medical oncology · 2025
    Article

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Esther BaranovDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School.
Matthew J McBrideDepartment of Pediatric Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
Andrew M BellizziDepartment of Pathology, University of Iowa Hospitals and Clinics and Carver College of Medicine, Iowa City, IA.
Azra H LigonDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School.
Christopher D M FletcherDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School.
Cigall KadochDepartment of Pediatric Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
Jason L HornickDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School.
Brigham and Women's Hospital · USDana-Farber Cancer Institute · USHarvard University · USUniversity of Iowa Hospitals and Clinics · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
Reversing Oncogenic BAF Complex Structure & Function: New Therapeutic ApproachesDP2CA195762 · NCI · DANA-FARBER CANCER INST · PI KADOCH, CIGALL · 2014 to 2014
$2.6M
Cancer-Specific Targeting and Function of Mammalian SWI/SNF (BAF) Chromatin Remodeling ComplexesR01CA237241 · NCI · DANA-FARBER CANCER INST · PI KADOCH, CIGALL · 2019 to 2023
$2.0M
NCI NIH HHS DP2 CA195762NCI NIH HHS R01 CA237241
6 · The paper itself

Abstract

Synovial sarcoma (SS), an aggressive soft tissue sarcoma with a predilection for the extremities of young adults, harbors the pathognomonic t(X;18)(p11;q11) translocation, resulting in SS18-SSX rearrangements. SS includes monophasic, biphasic, and poorly differentiated variants, which show considerable histologic overlap with a range of other tumor types, making the diagnosis challenging on limited biopsies. Immunohistochemistry (IHC) is routinely used in the differential diagnosis; however, presently available markers lack specificity. Thus, cytogenetic or molecular genetic techniques are often employed to confirm the diagnosis. Here, we report the development and characterization of 2 novel antibodies: an SS18-SSX fusion-specific antibody (E9X9V, designed to the breakpoint) as well as an SSX-specific antibody (E5A2C, designed to the SSX C-terminus). We validated the selectivity and specificity of the antibodies using immunoblotting, immunoprecipitation, and chromatin immunoprecipitation followed by next-generation sequencing in SS cell lines and demonstrated that both antibodies capture SS18-SSX on chromatin at established target sites (eg, TLE1 and BCL2) genome-wide. Using IHC in whole sections from 400 tumors including 100 genetically confirmed cases of SS and 300 histologic mimics, the SS18-SSX fusion-specific antibody revealed strong diffuse nuclear staining in 95 of 100 (95%) SS cases, whereas none of the 300 control tumors showed any staining. The SSX antibody showed strong diffuse nuclear staining in all 100 (100%) SS cases; 13 (4%) of the 300 other tumors were also positive, 5 of which displayed >50% nuclear staining. In summary, a novel SS18-SSX fusion-specific antibody is highly sensitive (95%) and specific (100%) for SS, and an antibody to the SSX C-terminus is also highly sensitive (100%), but slightly less specific (96%). IHC using the SS18-SSX antibody could replace molecular genetic or cytogenetic testing in most cases, and these reagents together will also provide the research community with valuable tools for further biochemical and genomic interrogation of the SS18-SSX fusion protein.

Indexed as

Antibodies, MonoclonalAnimalsBiomarkers, TumorCase-Control StudiesCell Line, TumorHigh-Throughput Nucleotide SequencingHumansImmunoblottingImmunoprecipitationIn Situ Hybridization, FluorescenceNeoplasm ProteinsOncogene Proteins, FusionProto-Oncogene ProteinsRabbitsRepressor ProteinsSarcoma, SynovialAntibodies, MonoclonalBiomarkers, Tumormonoclonal antibody E5A2Cmonoclonal antibody E9X9VNeoplasm ProteinsOncogene Proteins, FusionProto-Oncogene ProteinsRepressor ProteinsSS18 protein, humansynovial sarcoma X breakpoint proteins

Identifiers

PMID32141887
PMCPMC7289668
OpenAlexW3010223792

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.