Evidence map›Paper›PMID 23873154›Full record

ArticleInternational journal of cancer2014

Human endogenous retrovirus type K antibodies and mRNA as serum biomarkers of early-stage breast cancer.

Feng Wang-Johanning, Ming Li, Francisco J Esteva, Kenneth R Hess, Bingnan Yin, Kiera Rycaj, Joshua B Plummer, Jeremy G Garza, Stefan Ambs, Gary L Johanning

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 2 pooled it
9.7field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 2 syntheses or guidelines pooled it, 117 citations in OpenAlex.

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21 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 1 country.

Feng Wang-JohanningDepartment of Veterinary Sciences, The University of Texas M.D. Anderson Cancer Center, Houston, TX; Department of Immunology, The University of Texas M.D. Anderson Cancer Center, Houston, TX; Graduate School of Biomedical Sciences, The University of Texas Health Science Center at Houston, Houston, TX.
Ming Li
Francisco J Esteva
Kenneth R Hess
Bingnan Yin
Kiera Rycaj
Joshua B Plummer
Jeremy G Garza
Stefan Ambs
Gary L Johanning
The University of Texas MD Anderson Cancer Center · USHouston Methodist · USNational Cancer Institute · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICHIE, ELLEN R · 1996 to 2011
$16.4M
Novel Markers for Disease Outcome in Breast CancerZIABC010887 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI AMBS, STEFAN · 2009 to 2025
$11.5M
The Molecular Profile of Prostate Tumors in African-American MenZIABC010624 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI AMBS, STEFAN · 2009 to 2025
$8.0M
NCI NIH HHS P30 CA016672NIEHS NIH HHS ES007784NIEHS NIH HHS P30 ES007784
6 · The paper itself

Abstract

A simple and accurate test to detect early-stage breast cancer has not been developed. Previous studies indicate that the level of human endogenous retrovirus type K (group HERV-K(HML-2)) transcription may be increased in human breast tumors. We hypothesized that HERV-K(HML-2) reactivation can serve as a biomarker for early detection of breast cancer. Serum samples were collected from women without cancer (controls) and patients with ductal carcinoma in situ (DCIS) and invasive breast cancer. ELISA assays were used to detect serum anti-HERV-K(HML-2) antibody titers. RNA was extracted from sera and analyzed by real-time RT-PCR to quantitate the level of HERV-K(HML-2) mRNA. We measured significantly higher serum mRNA and serum antibody titers against HERV-K(HML-2) proteins in women with DCIS and stage I disease than in women without cancer. At optimized cutoffs for the antibody titers, the assay produced an area under the receiver operating characteristic curve (AUC) of 0.89 (95% confidence interval 0.77-1.00) for DCIS and of 0.95 (95% confidence interval 0.89-1.00) for invasive breast cancer. These AUCs are comparable to those observed for mammograms. We also found that serum HERV-K(HML-2) mRNA tended to be higher in breast cancer patients with a primary tumor who later on developed the metastatic disease than in patients who did not develop cancer metastasis. Our results show that HERV-K(HML-2) antibodies and mRNA are already elevated in the blood at an early stage of breast cancer, and further increase in patients who are at risk of developing a metastatic disease.

Indexed as

Antibodies, ViralBiomarkers, TumorBreast NeoplasmsCarcinoma, Intraductal, NoninfiltratingEndogenous RetrovirusesEnzyme-Linked Immunosorbent AssayFemaleHumansNeoplasm MetastasisReal-Time Polymerase Chain ReactionRNA, MessengerRNA, ViralAntibodies, ViralBiomarkers, TumorRNA, MessengerRNA, Viralbiomarkersbreast cancerearly detectionendogenous retrovirusesHERV-Kmetastasis

Identifiers

PMID23873154
PMCPMC4191919
OpenAlexW2135060734

What OpenQuestion holds

Textmetadata
LicenceTDM
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.