Evidence map›Paper›PMID 33727696›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2021

Calcified chondroid mesenchymal neoplasms with FN1-receptor tyrosine kinase gene fusions including FGFR2, FGFR1, MERTK, NTRK1, and TEK: a molecular and clinicopathologic analysis.

Yajuan J Liu, Wenjing Wang, Jeffrey Yeh, Yu Wu, Jose G Mantilla, Christopher D M Fletcher, Robert W Ricciotti, Eleanor Y Chen

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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 59 citations in OpenAlex.

  1. Future oncology (London, England) · 2025
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  13. AccurateInternational journal of molecular sciences · 2025
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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

8 authors at 2 institutions in 1 country.

Yajuan J LiuDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, United States. yajuan@uw.edu.
Wenjing WangDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, United States.
Jeffrey YehDepartment of Biology, University of Washington, Seattle, WA, United States.
Yu WuDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, United States.
Jose G MantillaDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, United States.ORCID http://orcid.org/0000-0003-4752-6459
Christopher D M FletcherDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States.
Robert W RicciottiDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, United States.
Eleanor Y ChenDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, United States. eleanor2@uw.edu.ORCID http://orcid.org/0000-0003-4372-7560
University of Washington · USBrigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Translocations involving FN1 have been described in a variety of neoplasms that share the presence of a cartilage matrix and may also contain a variable extent of calcification. Fusions of FN1 to FGFR1 or FGFR2 have been reported in nine soft tissue chondromas, mostly demonstrated indirectly by FISH analysis. Delineation of FN1 fusions with various partner genes will facilitate our understanding of the pathogenesis and diagnostic classification of these neoplasms. In this study, we present molecular, clinical, and pathologic features of 12 cartilaginous soft tissue neoplasms showing a predilection for the TMJ region and the distal extremities. We analyzed for gene fusions with precise breakpoints using targeted RNA-seq with a 115-gene panel. We detected gene fusions in ten cases, including three novel fusions, FN1-MERTK, FN1-NTRK1, and FN1-TEK, each in one case, recurrent FN1-FGFR2 fusion in five cases, FN1-FGFR1 in one case, and FGFR1-PLAG1 in one case. The breakpoints in the 5' partner gene FN1 ranged from exons 11-48, retaining the domains of a signal peptide, FN1, FN2, and/or FN3, while the 3' partner genes retained the transmembrane domain, tyrosine kinase (TK) domains, and/or Ig domain. The tumors are generally characterized by nodular/lobular growth of polygonal to stellate cells within a chondroid matrix, often accompanied by various patterns of calcification, resembling those described for the chondroblastoma-like variant of soft tissue chondroma. Additional histologic findings include extensive calcium pyrophosphate dihydrate deposition in two cases and features resembling tenosynovial giant cell tumor (TGCT). Overall, while the tumors from our series show significant morphologic overlap with chondroblastoma-like soft tissue chondroma, we describe findings that expand the morphologic spectrum of these neoplasms and therefore refer to them as "calcified chondroid mesenchymal neoplasms." These neoplasms represent a spectrum of chondroid/cartilage matrix-forming tumors harboring FN1-receptor TK fusions that include those classified as soft tissue chondroma as well as chondroid TGCT.

Indexed as

AdultAgedCalcinosisc-Mer Tyrosine KinaseFemaleFibroblast Growth Factor 2FibronectinsHumansMaleMiddle AgedNeoplasms, Connective TissueOncogene FusionReceptor, Fibroblast Growth Factor, Type 1Receptor, TIE-2Receptor, trkASoft Tissue Neoplasmsc-Mer Tyrosine KinaseFGFR1 protein, humanFibroblast Growth Factor 2FibronectinsFN1 protein, humanMERTK protein, humanNTRK1 protein, humanReceptor, Fibroblast Growth Factor, Type 1Receptor, TIE-2Receptor, trkATEK protein, human

Identifiers

PMID33727696
OpenAlexW3136258228

What OpenQuestion holds

Textmetadata
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.