Evidence map›Paper›PMID 31544104›Full record

ArticleFrontiers in medicine2019

Chromosomal Heterogeneity of the G-401 Rhabdoid Tumor Cell Line: Unusual Partial 7p Trisomy.

Elizaveta Fasler-Kan, Nijas Aliu, Frank-Martin Haecker, Natalia Maltsev, Sabrina Ruggiero, Dietmar Cholewa, Andreas Bartenstein, Milan Milošević, Steffen M Berger

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 93% 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

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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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors at 6 institutions in 2 countries.

Elizaveta Fasler-KanDepartment of Pediatric Surgery, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Nijas AliuDepartment of Human Genetics, University Children's Hospital, Inselspital, Bern, Switzerland.
Frank-Martin HaeckerDepartment of Pediatric Surgery, Children's Hospital of Eastern Switzerland, St. Gallen, Switzerland.
Natalia MaltsevDepartment of Human Genetics and USA Computation Institute, University of Chicago, Chicago, IL, United States.
Sabrina RuggieroDepartment of Pediatric Surgery, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Dietmar CholewaDepartment of Pediatric Surgery, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Andreas BartensteinDepartment of Pediatric Surgery, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Milan MiloševićDepartment of Pediatric Surgery, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Steffen M BergerDepartment of Pediatric Surgery, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
University Hospital of Bern · CHOstschweizer Kinderspital · CHUniversity Children’s Hospital Bern · CHUniversity of Basel · CHUniversity of Bern · CHUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rhabdoid tumor is a very aggressive and hardly curable pediatric malignancy. It commonly starts in the kidneys but also can occur in the brain, liver, and other organs. The treatment of this tumor usually involves a combination of surgery, radiation, and chemotherapy. Because this tumor is rare, there is still limited experience with a defined standard of care. Cytogenetic analysis is an important routine method to monitor chromosomal aberrations. We have analyzed metaphases of the G-401 rhabdoid tumor cell line. In these cells we have observed metaphases with derivative chromosome 12 arising from partial trisomy 7p. With increasing passage number the numbers of metaphases having this derivative chromosome 12 were found to be higher. In passage number 2 only one metaphase had this pathological chromosome 12. By passage number 10 and passage number 15 about 25 and 95% of this derivative chromosome 12 were found, respectively. We were able to subclone G-401 cells by limiting dilutions and successfully separated cells having apparently normal karyotypes from cells having derivative chromosome 12. Using the cell proliferation assay we showed that clones possessing the derivative chromosome 12 grew more rapidly than clones with normal chromosomes. The cell cycle analysis confirmed this observation. Overall, in this study we describe for the first time a 7p triplication in a rare rhabdoid tumor of kidney. Both types of clones described in this study could be used as a preclinical model to study the involvement of partial chromosome 7 alterations in the development of rhabdoid tumors.

Indexed as

chromosomal aberrationFISH assayG-401 cell linepartial 7p trisomypathophysiologyproliferationrhabdoid tumor

Identifiers

PMID31544104
PMCPMC6729120
OpenAlexW2964364512

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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.