Evidence map›Paper›PMID 31358854›Full record

ArticleLeukemia2020

Soluble SLAMF7 promotes the growth of myeloma cells via homophilic interaction with surface SLAMF7.

Jiro Kikuchi, Mitsuo Hori, Hidekatsu Iha, Noriko Toyama-Sorimachi, Shotaro Hagiwara, Yoshiaki Kuroda, Daisuke Koyama, Tohru Izumi, Hiroshi Yasui, Atsushi Suzuki and 1 more

Abstract read
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In one paragraph

Article in Leukemia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 67 citations in OpenAlex.

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  10. Identification of Therapy-Induced Clonal Evolution and Resistance Pathways in Minimal Residual Clones in Multiple Myeloma through Single-Cell Sequencing.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
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  12. Current Novel Targeted Therapeutic Strategies in Multiple Myeloma.International journal of molecular sciences · 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 8 institutions in 1 country.

Jiro KikuchiDivision of Stem Cell Regulation, Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Tochigi, 329-0498, Japan.
Mitsuo HoriDepartment of Hematology, Ibaraki Prefectural Central Hospital, Kasama, Ibaraki, 309-1793, Japan.
Hidekatsu IhaDepartment of Microbiology, Oita University Faculty of Medicine, Yufu, Oita, 879-5593, Japan.ORCID http://orcid.org/0000-0002-0999-5636
Noriko Toyama-SorimachiDepartment of Molecular Immunology and Inflammation, Research Institute, National Center for Global Health and Medicine, Shinjuku, Tokyo, 162-8655, Japan.
Shotaro HagiwaraDepartment of Hematology, Tokyo Women's Medical University, Shinjuku, Tokyo, 162-8666, Japan.
Yoshiaki KurodaDivision of Stem Cell Regulation, Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Tochigi, 329-0498, Japan.
Daisuke KoyamaDivision of Stem Cell Regulation, Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Tochigi, 329-0498, Japan.
Tohru IzumiDivision of Hematology, Tochigi Cancer Center, Utsunomiya, Tochigi, 320-0834, Japan.
Hiroshi YasuiThe Institute of Medical Science, The University of Tokyo, Minato, Tokyo, 108-8639, Japan.ORCID http://orcid.org/0000-0003-0905-6855
Atsushi SuzukiOncology Division, Bristol-Myers Squibb K.K., Shinjuku, Tokyo, 163-1327, Japan.
Yusuke FurukawaDivision of Stem Cell Regulation, Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Tochigi, 329-0498, Japan. furuyu@jichi.ac.jp.ORCID http://orcid.org/0000-0002-7249-6418
Jichi Medical University · JPBristol-Myers Squibb (Japan) · JPIbaraki Prefectural Central Hospital · JPNational Center for Global Health and Medicine · JPOita University · JPThe University of Tokyo · JPTochigi Cancer Center · JPTokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SLAMF7 is expressed mainly on multiple myeloma (MM) cells and considered an ideal target for immunotherapeutic approaches. Indeed, elotuzumab, an anti-SLAMF7 antibody, is used for the treatment of MM in combination with immunomodulatory drugs. SLAMF7 is cleaved via unknown mechanisms and detected as a soluble form (sSLAMF7) exclusively in the serum of MM patients; however, little is known about the role of sSLAMF7 in MM biology. In this study, we found that sSLAMF7 enhanced the growth of MM cells via homophilic interaction with surface SLAMF7 and subsequent activation of the SHP-2 and ERK signaling pathways. Elotuzumab suppressed sSLAMF7-induced MM cell growth both in vitro and in vivo. Promoter analyses identified IKZF1 (Ikaros) as a pivotal transcriptional activator of the SLAMF7 gene. Pharmacological targeting of Ikaros by lenalidomide and its analog pomalidomide downregulated SLAMF7 expression and ameliorated the response of MM cells to sSLAMF7. Elotuzumab blocked the growth-promoting function of sSLAMF7 when combined with lenalidomide in a murine xenograft model. Neutralization of sSLAMF7 is a novel antimyeloma mechanism of elotuzumab, which is enhanced by immunomodulatory drugs via downregulation of surface SLAMF7 expression on MM cells. These findings may provide important information for the optimal use of elotuzumab in MM treatment.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCell ProliferationHumansLenalidomideMiceMice, Inbred NODMice, SCIDMultiple MyelomaSignaling Lymphocytic Activation Molecule FamilyThalidomideXenograft Model Antitumor AssaysAntibodies, Monoclonal, HumanizedelotuzumabLenalidomidepomalidomideSignaling Lymphocytic Activation Molecule FamilySLAMF7 protein, humanThalidomide

Identifiers

PMID31358854
OpenAlexW2964412249

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.