Evidence map›Paper›PMID 24889268›Full record

ArticleBritish journal of haematology2014

High throughput quantitative reverse transcription PCR assays revealing over-expression of cancer testis antigen genes in multiple myeloma stem cell-like side population cells.

Jianguo Wen, Hangwen Li, Wenjing Tao, Barbara Savoldo, Jessica A Foglesong, Lauren C King, Youli Zu, Chung-Che Chang

Open access · greenAbstract read
In one paragraph

Article in British journal of haematology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Identification of CD8Frontiers in immunology · 2022
    Article
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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

8 authors at 5 institutions in 1 country.

Jianguo WenDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, USA.
Hangwen Li
Wenjing Tao
Barbara Savoldo
Jessica A Foglesong
Lauren C King
Youli Zu
Chung-Che Chang
Methodist Hospital · USThe University of Texas MD Anderson Cancer Center · USAdventHealth Orlando · USBaylor College of Medicine · USMichigan Center for Translational Pathology · US

Funding

A bifunctional nanomedicine for both specific imaging and targeting therapy of anR01CA151955 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI ZU, YOULI · 2010 to 2014
$1.5M
RFA-CA -12-003 - Activatable One-Drop and One-Step Assay for Circulating Tumor CeR33CA173382 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI ZU, YOULI · 2012 to 2014
$1.1M
Myeloma stem cell and cancer testis antigensR21CA150109 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI SAVOLDO, BARBARA, WEN, JIANGUO · 2010 to 2011
$380k
NCI NIH HHS R01 CA151955NCI NIH HHS R21 CA150109NCI NIH HHS R33 CA173382NCI NIH HHS R33CA173382PHS HHS R21/RCA150109A
6 · The paper itself

Abstract

Multiple myeloma (MM) stem cells, proposed to be responsible for the tumourigenesis, drug resistance and recurrence of this disease, are enriched in the cancer stem cell-like side population (SP). Cancer testis antigens (CTA) are attractive targets for immunotherapy because they are widely expressed in cancers but only in limited types of normal tissues. We designed a high throughput assay, which allowed simultaneous relative quantifying expression of 90 CTA genes associated with MM. In the three MM cell lines tested, six CTA genes were over-expressed in two and LUZP4 and ODF1 were universally up-regulated in all three cell lines. Subsequent study of primary bone marrow (BM) from eight MM patients and four healthy donors revealed that 19 CTA genes were up-regulated in SP of MM compared with mature plasma cells. In contrast, only two CTA genes showed a moderate increase in SP cells of healthy BM. Furthermore, knockdown using small interfering RNA (siRNA) revealed that LUZP4 expression is required for colony-forming ability and drug resistance in MM cells. Our findings indicate that multiple CTA have unique expression profiles in MM SP, suggesting that CTA may serve as targets for immunotherapy that it specific for MM stem cells and which may lead to the long-term cure of MM.

Indexed as

Antigens, NeoplasmApoptosisBiomarkers, TumorCell Line, TumorDNA-Binding ProteinsHeat-Shock ProteinsHigh-Throughput Screening AssaysHumansMultiple MyelomaNeoplastic Stem CellsReverse Transcriptase Polymerase Chain ReactionAntigens, NeoplasmBiomarkers, TumorDNA-Binding ProteinsHeat-Shock ProteinsLUZP4 protein, humanODF1 protein, humancancer testis antigenhigh throughputmultiple myelomaquantitative RT-PCRside population

Identifiers

PMID24889268
PMCPMC4365818
OpenAlexW2138175348

What OpenQuestion holds

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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.