Evidence map›Paper›PMID 34464480›Full record

ArticleCancer science2021

CD146 is a potential immunotarget for neuroblastoma.

Satoshi Obu, Katsutsugu Umeda, Hiroo Ueno, Mari Sonoda, Keiji Tasaka, Hideto Ogata, Kagehiro Kouzuki, Seishiro Nodomi, Satoshi Saida, Itaru Kato and 17 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2021. 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
1.5field-weighted citation impact, top 15% 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, 14 citations in OpenAlex.

  1. Review
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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

27 authors at 4 institutions in 1 country.

Satoshi ObuDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Katsutsugu UmedaDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-6844-2011
Hiroo UenoDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0001-7617-1672
Mari SonodaDepartment of Pediatric Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Keiji TasakaDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-2708-3876
Hideto OgataDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Kagehiro KouzukiDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Seishiro NodomiDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Satoshi SaidaDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-8930-3539
Itaru KatoDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-2932-4960
Hidefumi HiramatsuDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-3136-5670
Tatsuya OkamotoDepartment of Pediatric Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-1958-0714
Eri OgawaDepartment of Pediatric Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-3642-8802
Hideaki OkajimaDepartment of Pediatric Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-4043-1070
Ken MoritaDepartment of Human Health Science, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-6639-5274
Yasuhiko KamikuboDepartment of Human Health Science, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-2761-8508
Koji KawaguchiDepartment of Hematology and Oncology, Shizuoka Children's Hospital, Shizuoka, Japan.ORCID https://orcid.org/0000-0002-4612-4047
Kenichiro WatanabeDepartment of Hematology and Oncology, Shizuoka Children's Hospital, Shizuoka, Japan.ORCID https://orcid.org/0000-0002-8892-3082
Hideto IwafuchiDepartment of Pathology, Shizuoka Children's Hospital, Shizuoka, Japan.ORCID https://orcid.org/0000-0002-7755-9676
Shigeki YagyuDepartment of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0003-4256-9783
Tomoko IeharaDepartment of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0003-1740-7096
Hajime HosoiDepartment of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-8345-0159
Tatsutoshi NakahataDrug Discovery Technology Development Office, Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-0427-8440
Souichi AdachiDepartment of Human Health Science, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-8473-0187
Shinji UemotoDepartment of Pediatric Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-0126-9346
Toshio HeikeDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-6373-3442
Junko TakitaDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-2452-6520
Kyoto University · JPKyoto Prefectural University of Medicine · JPShizuoka Children's Hospital · JPKanazawa Medical University · JP

Funding

Japan Agency for Medical Research and Development 19ck0106468h0001
6 · The paper itself

Abstract

Neuroblastoma, the most common extracranial solid tumor of childhood, is thought to arise from neural crest-derived immature cells. The prognosis of patients with high-risk or recurrent/refractory neuroblastoma remains quite poor despite intensive multimodality therapy; therefore, novel therapeutic interventions are required. We examined the expression of a cell adhesion molecule CD146 (melanoma cell adhesion molecule [MCAM]) by neuroblastoma cell lines and in clinical samples and investigated the anti-tumor effects of CD146-targeting treatment for neuroblastoma cells both in vitro and in vivo. CD146 is expressed by 4 cell lines and by most of primary tumors at any stage. Short hairpin RNA-mediated knockdown of CD146, or treatment with an anti-CD146 polyclonal antibody, effectively inhibited growth of neuroblastoma cells both in vitro and in vivo, principally due to increased apoptosis via the focal adhesion kinase and/or nuclear factor-kappa B signaling pathway. Furthermore, the anti-CD146 polyclonal antibody markedly inhibited tumor growth in immunodeficient mice inoculated with primary neuroblastoma cells. In conclusion, CD146 represents a promising therapeutic target for neuroblastoma.

Indexed as

AnimalsAntibodiesApoptosisCD146 AntigenCell Line, TumorCell SurvivalFocal Adhesion Kinase 1Focal Adhesion Protein-Tyrosine KinasesGene Knockdown TechniquesHeterograftsHumansMiceMolecular Targeted TherapyNeoplasm Recurrence, LocalNeoplasm TransplantationNeuroblastomaAntibodiesCD146 AntigenFocal Adhesion Kinase 1Focal Adhesion Protein-Tyrosine KinasesNF-kappa BPTK2 protein, humanRNA, Small InterferingantibodyapoptosisCD146focal adhesion kinaseneuroblastoma

Identifiers

PMID34464480
PMCPMC8586675
OpenAlexW3198739350

What OpenQuestion holds

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LicenceCC BY-NC
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.