Evidence map›Paper›PMID 24482753›Full record

ArticleOncoimmunology2013

Murine leukemia virus envelope gp70 is a shared biomarker for the high-sensitivity quantification of murine tumor burden.

Francesca Scrimieri, David Askew, David J Corn, Saada Eid, Iuliana D Bobanga, Jaclyn A Bjelac, Matthew L Tsao, Frederick Allen, Youmna S Othman, Shih-Chung G Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

40 citing papers in PubMed, 59 citations in OpenAlex.

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  15. IL25American journal of cancer research · 2023
    Article
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  19. Position-Scanning Peptide Libraries as Particle Immunogens for Improving CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  20. Cancer therapy in mice using a pure population of CD8Cancer immunology, immunotherapy : CII · 2021
    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 at 3 institutions in 2 countries.

Francesca ScrimieriDepartment of Pediatrics; Case Western Reserve University School of Medicine; Cleveland, OH USA.
David AskewDepartment of Pediatrics; Case Western Reserve University School of Medicine; Cleveland, OH USA.
David J CornDepartment of Biomedical Engineering; Case Western Reserve University School of Medicine; Cleveland, OH USA.
Saada EidDepartment of Pediatrics; Case Western Reserve University School of Medicine; Cleveland, OH USA.
Iuliana D BobangaDepartment of Surgery; Case Western Reserve University School of Medicine; Cleveland, OH USA.
Jaclyn A BjelacDepartment of Pediatrics; Case Western Reserve University School of Medicine; Cleveland, OH USA.
Matthew L TsaoDepartment of Pediatrics; Case Western Reserve University School of Medicine; Cleveland, OH USA.
Frederick AllenDepartment of Pediatrics; Case Western Reserve University School of Medicine; Cleveland, OH USA.
Youmna S OthmanPediatric Hematology and Oncology; Stormont Vail Hospital; Cotton-O'Neil Cancer Center; Topeka, KS USA.
Shih-Chung G WangDepartment of Pediatrics; Changhua Christian Hospital; Changhua, Taiwan.
Alex Y HuangDepartment of Pediatrics; Case Western Reserve University School of Medicine; Cleveland, OH USA.
Case Western Reserve University · USChanghua Christian Hospital · TWColmery-O'Neil VA Medical Center · US

Funding

TRAINING PROGRAM IN MUSCULOSKELETAL RESEARCHT32AR007505 · NIAMS · CASE WESTERN RESERVE UNIVERSITY · PI TRIOLO, RONALD J · 1986 to 2023
$6.3M
Mechanistic Dynamic Study of Intranodal Chemokine-aided Antitumor Immune PrimingR01CA154656 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 2011 to 2015
$1.7M
NCI NIH HHS R01 CA154656NIAMS NIH HHS T32 AR007505
6 · The paper itself

Abstract

The preclinical development of anticancer drugs including immunotherapeutics and targeted agents relies on the ability to detect minimal residual tumor burden as a measure of therapeutic efficacy. Real-time quantitative (qPCR) represents an exquisitely sensitive method to perform such an assessment. However, qPCR-based applications are limited by the availability of a genetic defect associated with each tumor model under investigation. Here, we describe an off-the-shelf qPCR-based approach to detect a broad array of commonly used preclinical murine tumor models. In particular, we report that the mRNA coding for the envelope glycoprotein 70 (gp70) encoded by the endogenous murine leukemia virus (MuLV) is universally expressed in 22 murine cancer cell lines of disparate histological origin but is silent in 20 out of 22 normal mouse tissues. Further, we detected the presence of as few as 100 tumor cells in whole lung extracts using qPCR specific for gp70, supporting the notion that this detection approach has a higher sensitivity as compared with traditional tissue histology methods. Although gp70 is expressed in a wide variety of tumor cell lines, it was absent in inflamed tissues, non-transformed cell lines, or pre-cancerous lesions. Having a high-sensitivity biomarker for the detection of a wide range of murine tumor cells that does not require additional genetic manipulations or the knowledge of specific genetic alterations present in a given neoplasm represents a unique experimental tool for investigating metastasis, assessing antitumor therapeutic interventions, and further determining tumor recurrence or minimal residual disease.

Indexed as

AH1gp70minimal residual diseaseMuLVretrovirustumor-associated antigen

Identifiers

PMID24482753
PMCPMC3894233
OpenAlexW2084289643

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.