Evidence map›Paper›PMID 34069790›Full record

ArticleCancers2021

Familial Occurrence of Adult Granulosa Cell Tumors: Analysis of Whole-Genome Germline Variants.

Joline F Roze, Joachim Kutzera, Wouter Koole, Margreet G E M Ausems, Kristi Engelstad, Jurgen M J Piek, Cor D de Kroon, René H M Verheijen, Gijs van Haaften, Ronald P Zweemer and 1 more

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Joline F RozeDepartment of Gynaecological Oncology, UMC Utrecht Cancer Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.
Joachim KutzeraDepartment of Genetics, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.
Wouter KooleDepartment of Genetics, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.
Margreet G E M AusemsDepartment of Genetics, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.
Kristi EngelstadFM Ambulance, Fargo, ND 58078, USA.
Jurgen M J PiekDepartment of Obstetrics and Gynaecology, Catharina Hospital, 5623 EJ Eindhoven, The Netherlands.ORCID 0000-0002-0487-0631
Cor D de KroonDepartment of Obstetrics and Gynaecology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0002-7999-4161
René H M VerheijenDepartment of Gynaecological Oncology, UMC Utrecht Cancer Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.
Gijs van HaaftenDepartment of Genetics, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.ORCID 0000-0003-3033-0329
Ronald P ZweemerDepartment of Gynaecological Oncology, UMC Utrecht Cancer Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.
Glen R MonroeDepartment of Gynaecological Oncology, UMC Utrecht Cancer Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Funding

Granulosa Fund Philine van Esch not applicable
6 · The paper itself

Abstract

Adult granulosa cell tumor (AGCT) is a rare ovarian cancer subtype, with a peak incidence around 50-55 years. Although AGCT can occur in specific syndromes, a genetic predisposition for AGCT has not been identified. The aim of this study is to identify a genetic variant in families with AGCT patients, potentially contributing to tumor evolution. We identified four families, each including two women diagnosed with AGCT. Whole-genome sequencing was performed to identify overlapping germline variants or affected genes. Familial relationship was evaluated using genealogy and genomic analyses. Patient characteristics, medical (family) history, and pedigrees were collected. Findings were compared to a reference group of 33 unrelated AGCT patients. Mean age at diagnosis was 38 years (range from 17 to 60) versus 51 years in the reference group, and seven of eight patients were premenopausal. In two families, three first degree relatives were diagnosed with breast cancer. Furthermore, polycystic ovary syndrome (PCOS) and subfertility was reported in three families. Predicted deleterious variants in PIK3C2G, BMP5, and LRP2 were identified. In conclusion, AGCTs occur in families and could potentially be hereditary. In these families, the age of AGCT diagnosis is lower and cases of breast cancer, PCOS, and subfertility are present. We could not identify an overlapping genetic variant or affected locus that may explain a genetic predisposition for AGCT.

Indexed as

FOXL2granulosa cell tumorovarian cancersex cord-stromal tumorswhole-genome sequencing

Identifiers

PMID34069790
PMCPMC8157239

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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.