Evidence map›Paper›PMID 38191242›Full record

ArticleJournal for immunotherapy of cancer2024

Clearing soluble MIC reverses the impaired function of natural killer cells from patients with multiple myeloma.

Sojeong Kim, Haerim Chung, Jeong-Eun Kwak, Yu Ri Kim, Chung Hyun Park, Yeonhee Kim, June-Won Cheong, Jennifer Wu, Eui-Cheol Shin, Hyunsoo Cho and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Review
  6. Novel and potent MICA/B antibody is therapeutically effective inJournal for immunotherapy of cancer · 2025
    Article
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.

Sojeong Kim *Division of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Haerim Chung *Division of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Jeong-Eun Kwak *Division of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of).ORCID 0000-0003-3178-0823
Yu Ri KimDivision of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Chung Hyun ParkDivision of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Yeonhee KimDivision of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
June-Won CheongDivision of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Jennifer WuDepartment of Urology and Department of Microbiology and Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Eui-Cheol ShinGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Korea (the Republic of) hyunsoocho@yuhs.ac hemakim@yuhs.ac ecshin@kaist.ac.kr.ORCID 0000-0002-6308-9503
Hyunsoo ChoDivision of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of) hyunsoocho@yuhs.ac hemakim@yuhs.ac ecshin@kaist.ac.kr.ORCID 0000-0003-2651-6403
Jin Seok KimDivision of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of) hyunsoocho@yuhs.ac hemakim@yuhs.ac ecshin@kaist.ac.kr.
Yonsei University · KRKorea Advanced Institute of Science and Technology · KRNorthwestern University · US

Funding

Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
Tumor immune and glycan biomarkers for progressive prostate cancerR01CA212409 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., DRAKE, RICHARD R. · 2018 to 2022
$2.7M
Target MIC shedding to revive anti-tumor immunityR01CA204021 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WU, JENNIFER D · 2016 to 2022
$1.8M
NCI NIH HHS P50 CA180995NCI NIH HHS R01 CA204021
6 · The paper itself

Abstract

backgroundMajor histocompatibility complex (MHC) class I chain-related protein (MIC) is a stress-induced ligand released from multiple myeloma (MM) cells during progression, and soluble MIC impairs natural killer group 2D (NKG2D) activating receptor-mediated recognition and function of natural killer (NK) cells. However, whether clearing soluble MIC with a monoclonal antibody (mAb) can restore NK cell activity of MM patients remains undetermined.

methodsWe analyzed The Cancer Genome Atlas (TCGA) Multiple Myeloma Research Foundation (MMRF) CoMMpass data set to examine the prognostic significance of

resultsWe characterize the importance of MICA in MM by revealing the significantly better overall survival of patients with high

conclusionsOur findings indicate targeting soluble MIC with huB10G5 might be a viable therapeutic approach to promote NKG2D-dependent cellular immunotherapy outcome in MM.

Indexed as

Multiple MyelomaAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedHumansKiller Cells, NaturalNK Cell Lectin-Like Receptor Subfamily KAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedNK Cell Lectin-Like Receptor Subfamily KImmunityImmunotherapy

Identifiers

PMID38191242
PMCPMC10806558
OpenAlexW4390706808

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.