Evidence map›Paper›PMID 29765374›Full record

ArticleFrontiers in immunology2018

MICA-129 Dimorphism and Soluble MICA Are Associated With the Progression of Multiple Myeloma.

Alessandra Zingoni, Elisabetta Vulpis, Francesca Cecere, Maria G Amendola, Daniel Fuerst, Taron Saribekyan, Adnane Achour, Tatyana Sandalova, Ilaria Nardone, Agnese Peri and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 47 citations in OpenAlex.

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  11. Associations between MICA and MICB Genetic Variants, Protein Levels, and Colorectal Cancer: Atherosclerosis Risk in Communities (ARIC).Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023
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  19. Journal of personalized medicine · 2021
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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

19 authors at 4 institutions in 3 countries.

Alessandra ZingoniDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Elisabetta VulpisDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Francesca CecereDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Maria G AmendolaDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Daniel FuerstGerman Red Cross Blood Donor Services, Baden-Wuerttemberg-Hessia, Ulm, Germany.
Taron SaribekyanGerman Red Cross Blood Donor Services, Baden-Wuerttemberg-Hessia, Ulm, Germany.
Adnane AchourScience for Life Laboratory, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Tatyana SandalovaScience for Life Laboratory, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Ilaria NardoneDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Agnese PeriDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Alessandra SorianiDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Cinzia FiondaDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Elena MariggiòDepartment of Cellular Biotechnologies and Hematology, "Sapienza" University of Rome, Rome, Italy.
Maria T PetrucciDepartment of Cellular Biotechnologies and Hematology, "Sapienza" University of Rome, Rome, Italy.
Maria R RicciardiDepartment of Clinical and Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Joannis MytilineosGerman Red Cross Blood Donor Services, Baden-Wuerttemberg-Hessia, Ulm, Germany.
Marco CippitelliDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Cristina CerboniDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Angela SantoniDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Sapienza University of Rome · ITIstituto Pasteur · ITGerman Red Cross · DEKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells are immune innate effectors playing a pivotal role in the immunosurveillance of multiple myeloma (MM) since they are able to directly recognize and kill MM cells. In this regard, among activating receptors expressed by NK cells, NKG2D represents an important receptor for the recognition of MM cells, being its ligands expressed by tumor cells, and being able to trigger NK cell cytotoxicity. The MHC class I-related molecule A (MICA) is one of the NKG2D ligands; it is encoded by highly polymorphic genes and exists as membrane-bound and soluble isoforms. Soluble MICA (sMICA) is overexpressed in the serum of MM patients, and its levels correlate with tumor progression. Interestingly, a methionine (Met) to valine (Val) substitution at position 129 of the α2 heavy chain domain classifies the MICA alleles into strong (

Indexed as

AllelesGenetic Predisposition to DiseasePolymorphism, GeneticAgedAged, 80 and overAmino Acid SubstitutionDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleGene Expression Regulation, NeoplasticGenetic Association StudiesGenotypeHistocompatibility Antigens Class IHumansImmunophenotypingKiller Cells, NaturalHistocompatibility Antigens Class IMHC class I-related chain ANK Cell Lectin-Like Receptor Subfamily KMICA polymorphismmultiple myelomanatural killer cellsNKG2D receptorpredictive biomarker

Identifiers

PMID29765374
PMCPMC5938351
OpenAlexW2802986564

What Socratic 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 Socratic graph.