Evidence map›Paper›PMID 33435153›Full record

ArticleCancers2021

Alterations of NK Cell Phenotype in the Disease Course of Multiple Myeloma.

Tatiana Pazina, Alexander W MacFarlane, Luca Bernabei, Essel Dulaimi, Rebecca Kotcher, Clinton Yam, Natalie A Bezman, Michael D Robbins, Eric A Ross, Kerry S Campbell and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.2field-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

48 citing papers in PubMed, 69 citations in OpenAlex.

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  15. Genome-wide transcriptome analysis of Aβ deposition on PET in a Korean cohort.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
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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

11 authors at 3 institutions in 2 countries.

Tatiana PazinaBlood Cell Development and Function Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Alexander W MacFarlaneBlood Cell Development and Function Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Luca BernabeiAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-0213-8914
Essel DulaimiDepartment of Pathology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Rebecca KotcherAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA 19104, USA.
Clinton YamAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA 19104, USA.
Natalie A BezmanBristol-Myers Squibb, Redwood City, CA 94063, USA.
Michael D RobbinsBristol-Myers Squibb, Cambridge, MA 02142, USA.
Eric A RossBiostatistics and Bioinformatics Facility, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Kerry S CampbellBlood Cell Development and Function Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.ORCID 0000-0003-4665-7326
Adam D CohenAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA 19104, USA.
Fox Chase Cancer Center · USUniversity of Pennsylvania · USBristol-Myers Squibb (United States) · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
Bristol-Myers Squibb CA204-016, CA204-157NCI NIH HHS P30 CA006927NIH HHS CA06927
6 · The paper itself

Abstract

Accumulating evidence demonstrates important roles for natural killer (NK) cells in controlling multiple myeloma (MM). A prospective flow cytometry-based analysis of NK cells in the blood and bone marrow (BM) of MM patient subgroups was performed (smoldering (SMM), newly diagnosed (ND), relapsed/refractory, (RR) and post-stem cell transplantation (pSCT)). Assessments included the biomarker expression and function of NK cells, correlations between the expression of receptors on NK cells with their ligands on myeloma cells, and comparisons between MM patient subgroups and healthy controls. The most striking differences from healthy controls were found in RR and pSCT patients, in which NK cells were less mature and expressed reduced levels of the activating receptors DNAM-1, NKG2D, and CD16. These differences were more pronounced in the BM than in blood, including upregulation of the therapeutic targets TIM3, TIGIT, ICOS, and GITR. Their expression suggests NK cells became exhausted upon chronic encounters with the tumor. A high expression of SLAMF7 on blood NK cells correlated with shorter progression-free survival. This correlation was particularly evident in ND patients, including on mature CD56

Indexed as

bloodbone marrowDNAM-1GITRmultiple myelomaNCRNK cellsNKG2DSLAMF7

Identifiers

PMID33435153
PMCPMC7827733
OpenAlexW3119039614

What OpenQuestion holds

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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.