Evidence map›Paper›PMID 29362220›Full record

ArticleCancer immunology research2018

Integration of Oncogenes via Sleeping Beauty as a Mouse Model of HPV16

Yi-Hsin Lin, Ming-Chieh Yang, Ssu-Hsueh Tseng, Rosie Jiang, Andrew Yang, Emily Farmer, Shiwen Peng, Talia Henkle, Yung-Nien Chang, Chien-Fu Hung and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 20 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

11 authors at 2 institutions in 2 countries.

Yi-Hsin LinDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Ming-Chieh YangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Ssu-Hsueh TsengDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Rosie JiangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Andrew YangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Emily FarmerDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Shiwen PengDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Talia HenkleDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Yung-Nien ChangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Chien-Fu HungDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland. chung2@jhmi.edu wutc@jhmi.edu.
T-C WuDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland. chung2@jhmi.edu wutc@jhmi.edu.
Johns Hopkins University · USTri-Service General Hospital · TW

Funding

Treatment of HIV- and HIV+ Patients with HPV16+ CIN2/3 Using pNGLV4a-hCRTE6E7L2 DNA vaccine administered intramuscularly via electroporationP50CA098252 · NCI · JOHNS HOPKINS UNIVERSITY · PI Richard Bruce Roden · 2003 to 2026
$53.5M
ENHANCING HPV-16 E6-SPECIFIC ANTITUMOR IMMUNITYR01CA114425 · NCI · JOHNS HOPKINS UNIVERSITY · PI WU, TZYY-CHOOU · 2005 to 2016
$3.0M
Molecular pathogenesis and host response following persistent E6/E7 expressionR21AI109259 · NIAID · JOHNS HOPKINS UNIVERSITY · PI HUNG, CHIEN-FU · 2014 to 2015
$446k
Innovative Strategy to Generate Antigen-Specific Cytotoxic LymphocytesR21CA194896 · NCI · JOHNS HOPKINS UNIVERSITY · PI HUNG, CHIEN-FU · 2015 to 2016
$388k
NCI NIH HHS P50 CA098252NCI NIH HHS R01 CA114425NCI NIH HHS R21 CA194896NIAID NIH HHS R21 AI109259
6 · The paper itself

Abstract

Human papillomavirus type 16 (HPV16) is the etiologic factor for cervical cancer and a subset of oropharyngeal cancers. Although several prophylactic HPV vaccines are available, no effective therapeutic strategies to control active HPV diseases exist. Tumor implantation models are traditionally used to study HPV-associated buccal tumors. However, they fail to address precancerous phases of disease progression and display tumor microenvironments distinct from those observed in patients. Previously, K14-E6/E7 transgenic mouse models have been used to generate spontaneous tumors. However, the rate of tumor formation is inconsistent, and the host often develops immune tolerance to the viral oncoproteins. We developed a preclinical, spontaneous, HPV16

Indexed as

Disease Models, AnimalMouth NeoplasmsOncogene Proteins, ViralPapillomavirus InfectionsTransposasesAnimalsCD8-Positive T-LymphocytesFemaleHuman papillomavirus 16Lymphatic MetastasisMiceMice, Inbred BALB CMice, Inbred C57BLMice, NudeVaccines, DNAOncogene Proteins, Viralsleeping beauty transposase, humanTransposasesVaccines, DNA

Identifiers

PMID29362220
PMCPMC6056342
OpenAlexW2786418019

What OpenQuestion holds

Textmetadata
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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.