Evidence map›Paper›PMID 31348591›Full record

ArticleCancer science2019

Cancer therapy with major histocompatibility complex-deficient and interferon β-producing myeloid cells derived from allogeneic embryonic stem cells.

Satoshi Umemoto, Miwa Haruta, Masataka Sakisaka, Tokunori Ikeda, Hirotake Tsukamoto, Yoshihiro Komohara, Motohiro Takeya, Yasuharu Nishimura, Satoru Senju

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Molecular characterization of colorectal cancer: A five-gene prognostic signature based on RNA-binding proteins.Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association
    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

9 authors at 2 institutions in 1 country.

Satoshi UmemotoDepartment of Immunogenetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0000-0002-4014-8216
Miwa HarutaDepartment of Immunogenetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Masataka SakisakaDepartment of Immunogenetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Tokunori IkedaDepartment of Clinical Investigation, Kumamoto University Hospital, Kumamoto, Japan.
Hirotake TsukamotoDepartment of Immunology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0000-0003-3214-1652
Yoshihiro KomoharaDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0000-0001-9723-0846
Motohiro TakeyaDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Yasuharu NishimuraDepartment of Immunogenetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Satoru SenjuDepartment of Immunogenetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Kumamoto University · JPKumamoto University Hospital · JP

Funding

AMED 16ck0106080h0003AMED 17lm0203040h0001JSPS KAKENHI 17H04272JSPS KAKENHI, Grants-in-Aid for Scientific Research on Innovative Areas 16H 06498
6 · The paper itself

Abstract

We previously established a method to generate myeloid cells with a proliferative capability from pluripotent stem cells and designated them iPS-ML. Human iPS-ML cells share features with physiological macrophages including the capability to infiltrate into cancer tissues. We observed therapeutic effects of human iPS-ML cells expressing interferon β (iPS-ML/interferon (IFN)-β) in xenograft cancer models. However, assessment of host immune system-mediated therapeutic and adverse effects of this therapy is impossible by xenograft models. We currently evaluated the therapeutic effects of a mouse equivalent of human iPS-ML/IFN, a mouse embryonic stem (ES) cell-derived myeloid cell line producing IFN (ES-ML/IFN). The ES-MLs producing IFN-β (β-ML) and IFN-γ (γ-ML) and originating from E14 ES cells derived from the 129 mouse strain (H-2

Indexed as

AnimalsCD8-Positive T-LymphocytesCell Line, TumorColonic NeoplasmsEmbryonic Stem CellsFemaleHistocompatibility AntigensHumansInduced Pluripotent Stem CellsInterferon-betaKiller Cells, NaturalLymphocytes, Tumor-InfiltratingMiceMice, Inbred BALB CMyeloid CellsTransplantation, HomologousHistocompatibility AntigensInterferon-betaembryonic stem cellimmunotherapyinterferonmacrophageMHC

Identifiers

PMID31348591
PMCPMC6778629
OpenAlexW2965520710

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.