Evidence map›Paper›PMID 25865228›Full record

ArticleOncotarget2015

Autoimmune response to PARP and BRCA1/BRCA2 in cancer.

Qing Zhu, Su-Xia Han, Cong-Ya Zhou, Meng-Jiao Cai, Li-Ping Dai, Jian-Ying Zhang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 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

6 authors at 2 institutions in 2 countries.

Qing ZhuDepartment of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University Medical Center, Xi'an, Shaanxi, P.R. China.
Su-Xia HanDepartment of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University Medical Center, Xi'an, Shaanxi, P.R. China.
Cong-Ya ZhouDepartment of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University Medical Center, Xi'an, Shaanxi, P.R. China.
Meng-Jiao CaiDepartment of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University Medical Center, Xi'an, Shaanxi, P.R. China.
Li-Ping DaiDepartment of Biological Sciences, The University of Texas at El Paso, El Paso, Texas, USA.
Jian-Ying ZhangDepartment of Biological Sciences, The University of Texas at El Paso, El Paso, Texas, USA.
First Affiliated Hospital of Xi'an Jiaotong University · CNThe University of Texas at El Paso · US

Funding

TCCG12MD007592 · NIMHD · UNIVERSITY OF TEXAS EL PASO · PI KIRKEN, ROBERT A. · 2012 to 2018
$19.4M
Autoantibodies to tumor-associated antigens as diagnostic biomarkers in liver canSC1CA166016 · NCI · UNIVERSITY OF TEXAS EL PASO · PI ZHANG, JIANYING · 2011 to 2014
$1.0M
NCI NIH HHS SC1 CA166016NCI NIH HHS SC1CA166016NIMHD NIH HHS 2G12MD007592NIMHD NIH HHS G12 MD007592
6 · The paper itself

Abstract

purposeTo determine the role of autoantibodies to PARP1 and BRCA1/BRCA2 which were involved in the synthetic lethal interaction in cancer.

methodsEnzyme-Linked Immunosorbent Assay (ELISA) was used to detect autoantibodies to PARP1 and BRCA1/BRCA2 in 618 serum samples including 131 from breast cancer, 94 from lung cancer, 34 from ovarian cancer, 107 from prostate cancer, 76 from liver cancer, 41 from pancreatic cancer and 135 from normal individuals. The positive sera with ELISA were confirmed by Western blot. Immunohistochemistry was used to examine the expression of PARP1 and BRCA1/BRCA2 in breast cancer.

resultsAutoantibody frequency to PARP1, BRCA1, and BRCA2 in cancer varied from 0% to 50%. When the sera from cancer patients were tested for the presence of autoantibodies to PARP1 and BRCA1/BRCA2, the autoantibody responses slightly decreased and the positive autoantibody reactions varied from 0% to 50.0%. This was significantly higher autoantibody responses to PARP1 and BRCA1/BRCA2 (especially to PARP1 and BRCA1) in ovarian cancer and breast cancer compared to normal control sera (P < 0.001 and P < 0.01). Immunohistochemistry indicated that Pathology Grade at diagnosis to PARP1 expression in breast cancer was different (P < 0.05).

conclusionsDifferent cancers have different profiles of autoantibodies. The autoantibodies to proteins involving the synthetic lethal interactions would be novel serological biomarker in some selective cancers.

Indexed as

AutoimmunityAdultAgedAged, 80 and overAutoantibodiesBiomarkers, TumorBlotting, WesternBRCA1 ProteinBRCA2 ProteinCase-Control StudiesEnzyme-Linked Immunosorbent AssayFemaleHumansImmunohistochemistryMaleMiddle AgedAutoantibodiesBiomarkers, TumorBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesautoantibodyautoimmuneDNA repair enzyme poly (ADP-Ribose) polymerase 1 (PARP1)/BRCA1/BRCA2synthetic lethalitytumor-associated antigen (TAA)

Identifiers

PMID25865228
PMCPMC4484477
OpenAlexW1857314794

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.