Evidence map›Paper›PMID 32158595›Full record

ReviewImmune network2020

Far Beyond Cancer Immunotherapy: Reversion of Multi-Malignant Phenotypes of Immunotherapeutic-Resistant Cancer by Targeting the NANOG Signaling Axis.

Se Jin Oh, Jaeyoon Lee, Yukang Kim, Kwon-Ho Song, Eunho Cho, Minsung Kim, Heejae Jung, Tae Woo Kim

Open access · diamondAbstract readReview
In one paragraph

Review in Immune network, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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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

8 authors at 3 institutions in 3 countries.

Se Jin OhDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul 02841, Korea.ORCID https://orcid.org/0000-0002-9591-5267
Jaeyoon LeeCollege of Science, College of Social Sciences and Humanities, Northeastern University, Boston, MA 02115, USA.ORCID https://orcid.org/0000-0002-5231-0284
Yukang KimKorea University College of Medicine, Seoul 02841, Korea.
Kwon-Ho SongDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul 02841, Korea.ORCID https://orcid.org/0000-0001-6547-1143
Eunho ChoDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul 02841, Korea.ORCID https://orcid.org/0000-0002-3409-2535
Minsung KimKorea University College of Medicine, Seoul 02841, Korea.
Heejae JungKorea University College of Medicine, Seoul 02841, Korea.
Tae Woo KimDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul 02841, Korea.ORCID https://orcid.org/0000-0001-6183-6010
Korea University · JPKorea University · KRNortheastern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer immunotherapy, in the form of vaccination, adoptive cellular transfer, or immune checkpoint inhibitors, has emerged as a promising practice within the field of oncology. However, despite the developing field's potential to revolutionize cancer treatment, the presence of immunotherapeutic-resistant tumor cells in many patients present a challenge and limitation to these immunotherapies. These cells not only indicate immunotherapeutic resistance, but also show multi-modal resistance to conventional therapies, abnormal metabolism, stemness, and metastasis. How can immunotherapeutic-resistant tumor cells render multi-malignant phenotypes? We reasoned that the immune-refractory phenotype could be associated with multi-malignant phenotypes and that these phenotypes are linked together by a factor that acts as the master regulator. In this review, we discussed the role of the embryonic transcription factor NANOG as a crucial master regulator we named "common factor" in multi-malignant phenotypes and presented strategies to overcome multi-malignancy in immunotherapeutic-resistant cancer by restraining the NANOG-mediated multi-malignant signaling axis. Strategies that blunt the NANOG axis could improve the clinical management of therapy-refractory cancer.

Indexed as

Common factorImmunotherapyMulti-malignant phenotypesNANOGTherapy-refractory cancer

Identifiers

PMID32158595
PMCPMC7049583
OpenAlexW3003844152

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.