Evidence map›Paper›PMID 34033669›Full record

ArticlePloS one2021

LPCAT1-TERT fusions are uniquely recurrent in epithelioid trophoblastic tumors and positively regulate cell growth.

Gavin R Oliver, Sofia Marcano-Bonilla, Jonathan Quist, Ezequiel J Tolosa, Eriko Iguchi, Amy A Swanson, Nicole L Hoppman, Tanya Schwab, Ashley Sigafoos, Naresh Prodduturi and 16 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

3 citing papers in PubMed, 14 citations in OpenAlex.

  1. Association ofBiomedicines · 2025
    Article
  2. Article
  3. 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

26 authors at 3 institutions in 1 country.

Gavin R OliverCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.ORCID 0000-0002-9948-3799
Sofia Marcano-BonillaCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Jonathan QuistCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Ezequiel J TolosaDivision of Oncology Research, Schulze Center for Novel Therapeutics, Department of Oncology, Mayo Clinic, Rochester, Minnesota, United States of America.
Eriko IguchiDivision of Oncology Research, Schulze Center for Novel Therapeutics, Department of Oncology, Mayo Clinic, Rochester, Minnesota, United States of America.
Amy A SwansonDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Nicole L HoppmanDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Tanya SchwabDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Ashley SigafoosDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Naresh ProdduturiCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Jesse S VossDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Shannon M KnightDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Jin ZhangDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Numrah FadraCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Raul UrrutiaDivision of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, United States of America.
Michael ZimmermanCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Jan B EganCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Anthony G BilyeuDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Jin JenDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Ema VerasSibley Memorial Hospital, Johns Hopkins Medicine, Washington, DC, United States of America.
Rema'a Al-SafiGynecologic Pathology, Histopathology and Cytology Units, Maternity Hospital, Kuwait City, Kuwait.
Matthew BlockCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Sarah KerrDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Martin E Fernandez-ZapicoDivision of Oncology Research, Schulze Center for Novel Therapeutics, Department of Oncology, Mayo Clinic, Rochester, Minnesota, United States of America.
John K SchoolmeesterDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, United States of America.
Eric W KleeCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Mayo Clinic · USJohns Hopkins University · USMayo Clinic in Florida · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
NCI NIH HHS P30 CA015083
6 · The paper itself

Abstract

Gestational trophoblastic disease (GTD) is a heterogeneous group of lesions arising from placental tissue. Epithelioid trophoblastic tumor (ETT), derived from chorionic-type trophoblast, is the rarest form of GTD with only approximately 130 cases described in the literature. Due to its morphologic mimicry of epithelioid smooth muscle tumors and carcinoma, ETT can be misdiagnosed. To date, molecular characterization of ETTs is lacking. Furthermore, ETT is difficult to treat when disease spreads beyond the uterus. Here using RNA-Seq analysis in a cohort of ETTs and other gestational trophoblastic lesions we describe the discovery of LPCAT1-TERT fusion transcripts that occur in ETTs and coincide with underlying genomic deletions. Through cell-growth assays we demonstrate that LPCAT1-TERT fusion proteins can positively modulate cell proliferation and therefore may represent future treatment targets. Furthermore, we demonstrate that TERT upregulation appears to be a characteristic of ETTs, even in the absence of LPCAT1-TERT fusions, and that it appears linked to copy number gains of chromosome 5. No evidence of TERT upregulation was identified in other trophoblastic lesions tested, including placental site trophoblastic tumors and placental site nodules, which are thought to be the benign chorionic-type trophoblast counterpart to ETT. These findings indicate that LPCAT1-TERT fusions and copy-number driven TERT activation may represent novel markers for ETT, with the potential to improve the diagnosis, treatment, and outcome for women with this rare form of GTD.

Indexed as

1-Acylglycerophosphocholine O-AcyltransferaseAdultBiomarkers, TumorCell ProliferationEpithelioid CellsFemaleGestational Trophoblastic DiseaseHumansMiddle AgedOncogene Proteins, FusionPregnancyTelomeraseTrophoblastic NeoplasmsUterine Neoplasms1-Acylglycerophosphocholine O-AcyltransferaseBiomarkers, TumorLpcat1 protein, humanOncogene Proteins, FusionTelomeraseTERT protein, human

Identifiers

PMID34033669
PMCPMC8148365
OpenAlexW3165861511

What OpenQuestion holds

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LicenceCC BY
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.