Evidence map›Paper›PMID 19587378›Full record

ArticleBlood2009

Identification of novel antigens with induced immune response in monoclonal gammopathy of undetermined significance.

Simona Blotta, Pierfrancesco Tassone, Rao H Prabhala, Piersandro Tagliaferri, David Cervi, Samir Amin, Jana Jakubikova, Yu-Tzu Tai, Klaus Podar, Constantine S Mitsiades and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-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

27 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. The Cancer-Immunity Cycle in Multiple Myeloma.ImmunoTargets and therapy · 2021
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Cancer immunoprevention.Current opinion in immunology · 2016
    Review
  15. Article
  16. Identification of a novel fusion gene, IRF2BP2-RARA, in acute promyelocytic leukemia.Journal of the National Comprehensive Cancer Network : JNCCN · 2015
    Article
  17. Article
  18. Article
  19. Article
  20. 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

14 authors at 4 institutions in 2 countries.

Simona BlottaJerome Lipper Multiple Myeloma Center and LeBow Institute for Myeloma Therapeutics, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Pierfrancesco Tassone
Rao H Prabhala
Piersandro Tagliaferri
David Cervi
Samir Amin
Jana Jakubikova
Yu-Tzu Tai
Klaus Podar
Constantine S Mitsiades
Alessandro Zullo
Brunella Franco
Kenneth C Anderson
Nikhil C Munshi
Dana-Farber Cancer Institute · USMagna Graecia University · ITHarvard University · USTelethon Institute Of Genetics And Medicine · IT

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
Targeting Myeloma Cell-Host Bone Marrow InteractionsP01CA078378 · NCI · DANA-FARBER CANCER INSTITUTE · PI RITZ, JEROME · 1998 to 2014
$26.2M
NCI NIH HHS P01 CA078378NCI NIH HHS P01 CA155258NCI NIH HHS P50 CA100707NCI NIH HHS P50CA-100707PHS HHS P01-78378PHS HHS R01-129494Telethon TGM06Z08
6 · The paper itself

Abstract

The transformation from monoclonal gammopathy of undetermined significance (MGUS) to multiple myeloma (MM) is thought to be associated with changes in immune processes. We have therefore used serologic analysis of recombinant cDNA expression library to screen the sera of MGUS patients to identify tumor-associated antigens. A total of 10 antigens were identified, with specific antibody responses in MGUS. Responses appeared to be directed against intracellular proteins involved in cellular functions, such as apoptosis (SON, IFT57/HIPPI), DNA and RNA binding (ZNF292, GPATCH4), signal transduction regulators (AKAP11), transcriptional corepressor (IRF2BP2), developmental proteins (OFD1), and proteins of the ubiquitin-proteasome pathway (PSMC1). Importantly, the gene responsible for the oral-facial-digital type I syndrome (OFD1) had response in 6 of 29 (20.6%) MGUS patients but 0 of 11 newly diagnosed MM patients. Interestingly, 3 of 11 (27.2%) MM patients after autologous stem cell transplantations showed responses to OFD1. We have confirmed T-cell responses against OFD1 in MGUS and observed down-regulation of GLI1/PTCH1 and p-beta-catenin after OFD1 knock-down with specific siRNA, suggesting its functional role in the regulation of Hh and Wnt pathways. These findings demonstrate OFD1 as an important immune target and highlight its possible role in signal transduction and tumorigenesis in MGUS and MM.

Indexed as

AgedAged, 80 and overApoptosis Regulatory ProteinsAutoantigensbeta CateninCarrier ProteinsDNA-Binding ProteinsDNA, ComplementaryFemaleHumansMaleMultiple MyelomaNuclear ProteinsParaproteinemiasPatched-1 ReceptorPatched ReceptorsApoptosis Regulatory ProteinsAutoantigensbeta CateninCarrier ProteinsDNA-Binding ProteinsDNA, ComplementaryIRF2BP2 protein, humanNuclear ProteinsOFD1 protein, humanPatched-1 ReceptorPatched ReceptorsProteinsPTCH1 protein, humanReceptors, Cell SurfaceRNA-Binding ProteinsTranscription Factors

Identifiers

PMID19587378
PMCPMC2759650
OpenAlexW2072246786

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.