Evidence map›Paper›PMID 32011345›Full record

ArticleThe American journal of surgical pathology2020

BCOR Expression in Mullerian Adenosarcoma: A Potential Diagnostic Pitfall.

Vidarshi Muthukumarana, Daniel J Fix, Simona Stolnicu, Kay J Park, Robert A Soslow, Ryma Benayed, Marc Ladanyi, Cristina R Antonescu, Sarah Chiang

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Clinicopathological and genomic characterization of BCORL1-driven high-grade endometrial stromal sarcomas.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  7. Targeted RNA expression profiling identifies high-grade endometrial stromal sarcoma as a clinically relevant molecular subtype of uterine sarcoma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  8. Review
  9. 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

9 authors at 4 institutions in 2 countries.

Vidarshi MuthukumaranaDepartment of Pathology, University of Texas Medical Branch, Galveston, TX.
Daniel J FixDepartment of Pathology, Hackensack University Medical Center, Hackensack, NJ.
Simona StolnicuDepartment of Pathology, University of Medicine, Pharmacy, Sciences and Technology of Targu Mures, Targu Mures, Romania.
Kay J ParkDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.
Robert A SoslowDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.
Ryma BenayedDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.
Marc LadanyiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.
Cristina R AntonescuDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.
Sarah ChiangDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.
Memorial Sloan Kettering Cancer Center · USHackensack University Medical Center · USThe University of Texas Medical Branch at Galveston · USUniversitatea de Medicină, Farmacie, Științe și Tehnologie „George Emil Palade” din Târgu Mureș · RO

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Adenosarcoma can mimic high-grade endometrial stromal sarcoma with ZC3H7B-BCOR fusion that may show entrapped glands and often exhibits diffuse BCOR expression. We encountered diffuse BCOR expression in rare adenosarcomas and sought to define its frequency among a larger cohort of these tumors. BCOR immunohistochemistry was performed on archival formalin-fixed paraffin-embedded tumor tissue in 13 of 14 adenosarcomas with and without stromal overgrowth arising in the uterus or ovary. The staining intensity and percentage of positive tumor nuclei in the mesenchymal component were evaluated. Eleven cases with sufficient tumoral tissue were subjected to fluorescence in situ hybridization for the detection of BCOR, BCORL1, NUTM1, ZC3H7B, and JAZF1 rearrangement. Three cases were subjected to targeted RNA sequencing. BCOR was expressed in 9 of 13 (70%) tumors, including 6 with and 3 without stromal overgrowth. Moderate to strong staining in >70% of cells was seen throughout in 1 low-grade and 6 high-grade tumors, 5 of which had stromal overgrowth. No staining was seen in 3 low-grade and 1 high-grade tumors with stromal overgrowth. One tumor demonstrating extensive sex cord-like differentiation and diffuse BCOR expression harbored JAZF1 and BCORL1 rearrangements. No BCOR or BCORL1 rearrangement was identified in the remaining tumors. BCOR expression is seen in most adenosarcomas with and without stromal overgrowth. BCORL1 rearrangement is seen in rare tumors with diffuse BCOR expression. Assessment of BCOR or BCORL1 rearrangement status is required in adenosarcomas demonstrating BCOR expression.

Indexed as

AdenosarcomaAdultAgedBiomarkers, TumorDiagnosis, DifferentialEndometrial NeoplasmsFemaleHumansMiddle AgedProto-Oncogene ProteinsRepressor ProteinsSarcoma, Endometrial StromalUterine NeoplasmsYoung AdultBCOR protein, humanBiomarkers, TumorProto-Oncogene ProteinsRepressor Proteins

Identifiers

PMID32011345
PMCPMC10189887
OpenAlexW3003467184

What OpenQuestion holds

Textmetadata
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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.