Evidence map›Paper›PMID 20359302›Full record

ArticleBioTechniques2010

Quantifying the relative amount of mouse and human DNA in cancer xenografts using species-specific variation in gene length.

Ming-Tseh Lin, Li-Hui Tseng, Hirohiko Kamiyama, Mihoko Kamiyama, Phillip Lim, Manuel Hidalgo, Sarah Wheelan, James Eshleman

Open access · goldAbstract read
In one paragraph

Article in BioTechniques, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 23% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Ming-Tseh LinThe Department of Pathology, Johns Hopkins University School of Medicine, Johns Hopkins Hospital, Baltimore, MD 21231, USA.
Li-Hui Tseng
Hirohiko Kamiyama
Mihoko Kamiyama
Phillip Lim
Manuel Hidalgo
Sarah Wheelan
James Eshleman
Johns Hopkins Medicine · USJohns Hopkins University · USJohns Hopkins Hospital · US

Funding

Tumor Antigens for Individual Signatures and TherapyP50CA062924 · NCI · JOHNS HOPKINS UNIVERSITY · PI LENNON, ANNE MARIE · 1993 to 2022
$54.6M
Novel Human Cancer Cell Isolation SystemR01CA130938 · NCI · JOHNS HOPKINS UNIVERSITY · PI ESHLEMAN, JAMES R. · 2008 to 2011
$1.2M
NCI NIH HHS P50-CA62924NCI NIH HHS R01 CA130938NCI NIH HHS R01-CA130938
6 · The paper itself

Abstract

Human cancer cell lines and xenografts are valuable samples for whole-genome sequencing of human cancer. Tumors can be maintained by serial xenografting in athymic (nude) or severe combined immunodeficient (SCID) mice. In the current study, we developed a molecular assay to quantify the relative contributions of human and mouse in mixed DNA samples. The assay was designed based on deletion/insertion variation between human and mouse genomes. The percentage of mouse DNA was calculated according to the relative peak heights of PCR products analyzed by capillary electrophoresis. Three markers from chromosomes 9 and 10 accurately predicted the mouse genome ratio and were combined into a multiplex PCR reaction. We used the assay to quantify the relative DNA amounts of 93 mouse xenografts used for a recently reported integrated genomic analysis of human pancreatic cancer. Of the 93 xenografts, the mean percentage of contaminating mouse DNA was 47%, ranging from 17% to 73%, with 43% of samples having >50% mouse DNA. We then comprehensively compared the human and mouse genomes to identify 370 additional candidate gene loci demonstrating human-mouse length variation. With increasing whole-genome sequencing of human cancers, this assay should be useful to monitor strategies to enrich human cancer cells from mixed human-mouse cell xenografts. Finally, we discuss how contaminating mouse DNA affects next-generation DNA sequencing.

Indexed as

GenomeNeoplasm TransplantationTransplantation, HeterologousAnimalsBase SequenceChromosome MappingDNAElectrophoresis, CapillaryHumansMiceMolecular Sequence DataPancreatic NeoplasmsPolymerase Chain ReactionPolymorphism, GeneticReproducibility of ResultsSequence Analysis, DNADNA

Identifiers

PMID20359302
PMCPMC3065779
OpenAlexW2123062855

What OpenQuestion holds

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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.