Evidence map›Paper›PMID 11895905›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2002

Autoimmunity to the M(r) 32,000 subunit of replication protein A in breast cancer.

J E Tomkiel, H Alansari, N Tang, J B Virgin, X Yang, P VandeVord, R L Karvonen, J L Granda, M J Kraut, J F Ensley and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 31% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. Pooled it
  2. Menin in Cancer.Genes · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Rtt105 promotes high-fidelity DNA replication and repair by regulating the single-stranded DNA-binding factor RPA.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Cdc45 is limiting for replication initiation in humans.Cell cycle (Georgetown, Tex.) · 2016
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Repair-specific functions of replication protein A.The Journal of biological chemistry · 2012
    Article
  20. Serologic laboratory findings in malignancy.Rheumatic diseases clinics of North America · 2011
    Review
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 1 institution in 1 country.

J E TomkielCenter for Molecular Medicine and Genetics, Karmanos Cancer Institute, Detroit, Michigan 48201, USA.
H Alansari
N Tang
J B Virgin
X Yang
P VandeVord
R L Karvonen
J L Granda
M J Kraut
J F Ensley
F Fernández-Madrid
The Barbara Ann Karmanos Cancer Institute · US

Funding

AUTOANTIBODIES AS MARKERS OF BREAST CANCERR21CA087759 · NCI · WAYNE STATE UNIVERSITY · PI FERNANDEZ-MADRID, FELIX · 2001 to 2002
$224k
NCI NIH HHS CA-87759-01NCI NIH HHS R21 CA087759NIAMS NIH HHS R21 AR-99-128
6 · The paper itself

Abstract

purposeWe sought to identify autoantigens recognized by antibodies in breast cancer patient sera with potential diagnostic or prognostic significance. EXPERIMENTAL

designSerum from a female breast cancer patient exhibiting a high titer antinuclear antibody was used to screen a HeLa cDNA expression library, leading to the cloning of a cDNA for the M(r) 32,000 subunit of replication protein A (RPA32). RPA32 expression and localization were assayed in autologous tumor by monoclonal antibody staining. A specific ELISA using recombinant protein was used to screen sera from 801 breast cancer patients and 65 controls.

resultsA relationship between anti-replication protein A (RPA) antibodies and the ductal breast carcinoma of the proband was suggested by overexpression and aberrant localization of RPA32 in tumor cells as compared with surrounding normal ductal tissue and by the presence of anti-RPA32 antibodies before the diagnosis. The prevalence of anti-RPA32 antibodies was significantly higher (P < 0.01) among breast cancer patients (87 of 801 patients) than among noncancer controls (0 of 65 controls). Similarly, anti-RPA32 antibodies were present in 4 of 39 patients with intraductal in situ carcinoma. No associations were found between anti-RPA antibodies and survival, occurrence of a second tumor, metastases, or antibodies to p53. Reactivity to RPA32 also was detected in sera from 3 of 47 patients with other cancers.

conclusionsIn view of the central role of RPA in DNA replication, recombination, and repair, we suggest that autoimmunity to RPA32 may reflect molecular changes involved in the process of tumorigenesis. The finding of antibodies to RPA32 before diagnosis and their prevalence in in situ carcinoma suggest that they are potentially useful markers of early disease.

Indexed as

Antigens, NeoplasmAutoantibodiesAutoantigensAutoimmunityBiomarkers, TumorBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma in SituCarcinoma, Squamous CellCase-Control StudiesCloning, MolecularDNA-Binding ProteinsEnzyme-Linked Immunosorbent AssayFemaleGene LibraryHead and Neck NeoplasmsAntigens, NeoplasmAutoantibodiesAutoantigensBiomarkers, TumorDNA-Binding ProteinsReplication Protein ARPA1 protein, humanTumor Suppressor Protein p53

Identifiers

PMID11895905
PMCPMC5604237
OpenAlexW1905950615

What OpenQuestion holds

Textmetadata
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.