Evidence map›Paper›PMID 38279992›Full record

ArticleCancer immunology, immunotherapy : CII2024

An analysis pipeline for understanding 6-thioguanine effects on a mouse tumour genome.

Patricio Yankilevich, Loulieta Nazerai, Shona Caroline Willis, Kjeld Schmiegelow, Daniela De Zio, Morten Nielsen

Open access · goldAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2024. 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
0.5field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  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

6 authors at 4 institutions in 2 countries.

Patricio YankilevichBioinformatics Core Facility, Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA) - CONICET - Partner Institute of the Max Planck Society, Buenos Aires, Argentina. pyankilevich@ibioba-mpsp-conicet.gov.ar.ORCID http://orcid.org/0000-0002-9606-1072
Loulieta NazeraiMelanoma Research Team, Danish Cancer Institute, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-1090-9029
Shona Caroline WillisMelanoma Research Team, Danish Cancer Institute, Copenhagen, Denmark.
Kjeld Schmiegelow *Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-0829-4993
Daniela De Zio *Melanoma Research Team, Danish Cancer Institute, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-9454-402X
Morten Nielsen *Department of Health Technology, Section for Bioinformatics, Technical University of Denmark, Lyngby, Denmark. morni@dtu.dk.ORCID http://orcid.org/0000-0001-7885-4311
Copenhagen University Hospital · DKBiomedicine Research Institute of Buenos Aires - CONICET - Partner Institute of the Max Planck Society · ARTechnical University of Denmark · DKUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mouse tumour models are extensively used as a pre-clinical research tool in the field of oncology, playing an important role in anticancer drugs discovery. Accordingly, in cancer genomics research, the demand for next-generation sequencing (NGS) is increasing, and consequently, the need for data analysis pipelines is likewise growing. Most NGS data analysis solutions to date do not support mouse data or require highly specific configuration for their use. Here, we present a genome analysis pipeline for mouse tumour NGS data including the whole-genome sequence (WGS) data analysis flow for somatic variant discovery, and the RNA-seq data flow for differential expression, functional analysis and neoantigen prediction. The pipeline is based on standards and best practices and integrates mouse genome references and annotations. In a recent study, the pipeline was applied to demonstrate the efficacy of low dose 6-thioguanine (6TG) treatment on low-mutation melanoma in a pre-clinical mouse model. Here, we further this study and describe in detail the pipeline and the results obtained in terms of tumour mutational burden (TMB) and number of predicted neoantigens, and correlate these with 6TG effects on tumour volume. Our pipeline was expanded to include a neoantigen analysis, resulting in neopeptide prediction and MHC class I antigen presentation evaluation. We observed that the number of predicted neoepitopes were more accurate indicators of tumour immune control than TMB. In conclusion, this study demonstrates the usability of the proposed pipeline, and suggests it could be an essential robust genome analysis platform for future mouse genomic analysis.

Indexed as

MelanomaThioguanineAnimalsGenomicsMiceMutationRNA-SeqThioguanine6-Thioguanine (6TG) treatmentImmune-checkpoint inhibitors (ICI)Mouse genome analysis pipelineMouse tumour modelsNeoantigen analysisTumour mutational burden

Identifiers

PMID38279992
PMCPMC10821971
OpenAlexW4391278312

What OpenQuestion holds

Textmetadata
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.