Evidence map›Paper›PMID 26883197›Full record

ArticleOncotarget2016

Induction of cancer testis antigen expression in circulating acute myeloid leukemia blasts following hypomethylating agent monotherapy.

Pragya Srivastava, Benjamin E Paluch, Junko Matsuzaki, Smitha R James, Golda Collamat-Lai, Nadja Blagitko-Dorfs, Laurie Ann Ford, Rafeh Naqash, Michael Lübbert, Adam R Karpf and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 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

12 authors at 4 institutions in 2 countries.

Pragya SrivastavaDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.
Benjamin E PaluchDepartment of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Buffalo, NY, USA.
Junko MatsuzakiCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, NY, USA.
Smitha R JamesDepartment of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Buffalo, NY, USA.
Golda Collamat-LaiDepartment of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Buffalo, NY, USA.
Nadja Blagitko-DorfsDepartment of Medicine, Division of Hematology/Oncology, University of Freiburg, Medical Center, Freiburg, Germany.
Laurie Ann FordDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.
Rafeh NaqashDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.
Michael LübbertDepartment of Medicine, Division of Hematology/Oncology, University of Freiburg, Medical Center, Freiburg, Germany.
Adam R KarpfEppley Institute for Cancer Research, Fred and Pamela Buffet Cancer Center, University of Nebraska Medical Center, Nebraska Medical Center, Omaha, NE, USA.
Michael J NemethDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.
Elizabeth A GriffithsDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.
Roswell Park Comprehensive Cancer Center · USUniversity Medical Center Freiburg · DEUniversity of Freiburg · DEUniversity of Nebraska Medical Center · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
RPCI-UPCI Ovarian Cancer SPOREP50CA159981 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MOYSICH, KIRSTEN B. · 2013 to 2025
$19.6M
DRUG DEVELOPMENT AND CANCER TREATMENTST32CA009072 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI JOHNSON, CANDACE S · 1985 to 2014
$2.3M
NCI NIH HHS P30 CA016056NCI NIH HHS P50 CA159981NCI NIH HHS T32 CA009072
6 · The paper itself

Abstract

Cancer testis antigens (CTAs) are promising cancer associated antigens in solid tumors, but in acute myeloid leukemia, dense promoter methylation silences their expression. Leukemia cell lines exposed to HMAs induce expression of CTAs. We hypothesized that AML patients treated with standard of care decitabine (20mg/m2 per day for 10 days) would demonstrate induced expression of CTAs. Peripheral blood blasts serially isolated from AML patients treated with decitabine were evaluated for CTA gene expression and demethylation. Induction of NY-ESO-1 and MAGEA3/A6, were observed following decitabine. Re-expression of NY-ESO-1 and MAGEA3/A6 was associated with both promoter specific and global (LINE-1) hypomethylation. NY-ESO-1 and MAGEA3/A6 mRNA levels were increased irrespective of clinical response, suggesting that these antigens might be applicable even in patients who are not responsive to HMA therapy. Circulating blasts harvested after decitabine demonstrate induced NY-ESO-1 expression sufficient to activate NY-ESO-1 specific CD8+ T-cells. Induction of CTA expression sufficient for recognition by T-cells occurs in AML patients receiving decitabine. Vaccination against NY-ESO-1 in this patient population is feasible.

Indexed as

AgedAged, 80 and overAntigens, NeoplasmAntineoplastic AgentsAzacitidineDecitabineFemaleHumansLeukemia, Myeloid, AcuteMaleMembrane ProteinsMiddle AgedAntigens, NeoplasmAntineoplastic AgentsAzacitidineCTAG1B protein, humanDecitabineMembrane Proteinsacute myeloid leukemiacancer testis antigendecitabineimmunotherapyNY-ESO-1

Identifiers

PMID26883197
PMCPMC4914325
OpenAlexW2300461615

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.