Evidence map›Paper›PMID 28477316›Full record

ArticleFamilial cancer2018

Gestational choriocarcinoma associated with a germline TP53 mutation.

Anne-Claire Brehin, Sophie Patrier-Sallebert, Gaëlle Bougeard, Gwendoline Side-Pfennig, Francisco Llamas Gutierrez, Aude Lamy, Elodie Colasse, Christine Kandel-Aznar, Capucine Delnatte, Eric Vuillemin and 5 more

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Familial cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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  5. Transmission of aCold Spring Harbor molecular case studies · 2018
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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

15 authors at 8 institutions in 1 country.

Anne-Claire BrehinDepartment of Pathology, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, F 76000, Rouen, France.
Sophie Patrier-SallebertDepartment of Pathology, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, F 76000, Rouen, France.
Gaëlle BougeardDepartment of Genetics, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, F 76000, Rouen, France.
Gwendoline Side-PfennigDepartment of Pathology, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, F 76000, Rouen, France.
Francisco Llamas GutierrezDepartment of Pathology, Rennes University Hospital, 35033, Rennes Cedex 9, France.
Aude LamyDepartment of Pathology, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, F 76000, Rouen, France.
Elodie ColasseDepartment of Pathology, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, F 76000, Rouen, France.
Christine Kandel-AznarDepartment of Pathology, Nantes University Hospital, Hôtel-Dieu, 44093, Nantes Cedex 1, France.
Capucine DelnatteDepartment of Cancer Genetics, CLCC René Gauducheau, Institut de Cancerologie de l'Ouest, 44805, Saint-Herblain, France.
Eric VuilleminDepartment of Oncology, Clinique Océane, 56000, Vannes, France.
Sophie Sadot-LebouvierDepartment of Oncology, CLCC René Gauducheau, Institut de Cancerologie de l'Ouest, 44805, Saint-Herblain, France.
Sylvie OdentDepartment of Genetics, Rennes University Hospital, 35033, Rennes, France.
Jean-Christophe SabourinDepartment of Pathology, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, F 76000, Rouen, France.
François GolfierFrench Trophoblastic Disease Reference Center, Lyon University Hospital, 69310, Pierre-Bénite, France.
Thierry FrebourgDepartment of Genetics, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, F 76000, Rouen, France. frebourg@chu-rouen.fr.
Inserm · FRInstitut de Cancérologie de l'Ouest · FRNormandie Université · FRUniversité de Rouen Normandie · FRCentre Hospitalier Universitaire de Rennes · FRHospices Civils de Lyon · FRInstitut de génétique et de développement de Rennes · FRNantes Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Choriocarcinoma is a highly malignant neoplasm resulting from the malignant transformation of proliferating trophoblastic cells and the molecular mechanisms leading to this transformation remain to be characterized. We report here the first case of a female germline TP53 mutation carrier who developed, as a first tumour, a lung choriocarcinoma, 6 months after a normal delivery. Molecular analyses established the gestational origin of the choriocarcinoma and showed, within the tumour, the presence of the germline mutant TP53 allele and loss of the wild-type allele. Resistance to methotrexate chemotherapy led to perform a surgical resection of the tumour. In agreement with the permissive role of TP53 mutations to oncogenic events, this report strongly suggests that TP53 mutations may promote malignant transformation of proliferating trophoblastic cells. Therefore, female TP53 mutation carriers may have an increased risk of developing gestational choriocarcinoma and might benefit from β-hCG level monitoring after pregnancy.

Indexed as

AdultChoriocarcinomaChorionic Gonadotropin, beta Subunit, HumanFemaleGerm-Line MutationHumansLungLung NeoplasmsMalePneumonectomyTumor Suppressor Protein p53Chorionic Gonadotropin, beta Subunit, HumanTP53 protein, humanTumor Suppressor Protein p53ChoriocarcinomaGestational choriocarcinomaGestational trophoblastic diseaseLi-Fraumeni syndromeTP53

Identifiers

PMID28477316
OpenAlexW2610237000

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.