Evidence map›Paper›PMID 31877663›Full record

ArticleCells2019

Synergistic Effects of Nanomedicine Targeting TNFR2 and DNA Demethylation Inhibitor-An Opportunity for Cancer Treatment.

Mohammad A I Al-Hatamleh, Engku Nur Syafirah E A R, Jennifer C Boer, Khalid Ferji, Jean-Luc Six, Xin Chen, Eyad Elkord, Magdalena Plebanski, Rohimah Mohamud

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  7. Article
  8. The role of TNFR2Life sciences · 2021
    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

9 authors at 5 institutions in 5 countries.

Mohammad A I Al-HatamlehDepartment of Immunology, School of Medical Sciences, Universiti Sains Malaysia, 16150 Kelantan, Malaysia.ORCID 0000-0001-8249-9519
Engku Nur Syafirah E A RDepartment of Medical Microbiology and Parasitology, School of Medical Sciences, Universiti Sains Malaysia, Kelantan 16150, Malaysia.ORCID 0000-0003-3249-6357
Jennifer C BoerTranslational Immunology and Nanotechnology Unit, School of Health and Biomedical Sciences, RMIT University, Bundoora 3083, Australia.
Khalid FerjiUniversité de Lorraine, CNRS, LCPM, F-5400 Nancy, France.ORCID 0000-0003-3073-9722
Jean-Luc SixUniversité de Lorraine, CNRS, LCPM, F-5400 Nancy, France.ORCID 0000-0003-1151-6953
Xin ChenState Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences. University of Macau, Macao 999078, China.
Eyad ElkordCancer Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation, 34110 Doha, Qatar.ORCID 0000-0002-3868-0318
Magdalena PlebanskiTranslational Immunology and Nanotechnology Unit, School of Health and Biomedical Sciences, RMIT University, Bundoora 3083, Australia.
Rohimah MohamudDepartment of Immunology, School of Medical Sciences, Universiti Sains Malaysia, 16150 Kelantan, Malaysia.ORCID 0000-0002-2465-6421
Universiti Sains Malaysia · MYCentre National de la Recherche Scientifique · FRRMIT University · AUHamad bin Khalifa University · QAUniversity of Macau · MO

Funding

Ministry of Higher Education, Malaysia 203/PPSP/6171198Universiti Sains Malaysia 1001/PPSP/8012294
6 · The paper itself

Abstract

Tumor necrosis factor receptor 2 (TNFR2) is expressed on some tumor cells, such as myeloma, Hodgkin lymphoma, colon cancer and ovarian cancer, as well as immunosuppressive cells. There is increasingly evidence that TNFR2 expression in cancer microenvironment has significant implications in cancer progression, metastasis and immune evasion. Although nanomedicine has been extensively studied as a carrier of cancer immunotherapeutic agents, no study to date has investigated TNFR2-targeting nanomedicine in cancer treatment. From an epigenetic perspective, previous studies indicate that DNA demethylation might be responsible for high expressions of TNFR2 in cancer models. This perspective review discusses a novel therapeutic strategy based on nanomedicine that has the capacity to target TNFR2 along with inhibition of DNA demethylation. This approach may maximize the anti-cancer potential of nanomedicine-based immunotherapy and, consequently, markedly improve the outcomes of the management of patients with malignancy.

Indexed as

Antineoplastic AgentsDNA DemethylationDrug SynergismEpigenesis, GeneticHumansNanomedicineNeoplasmsReceptors, Tumor Necrosis Factor, Type IISignal TransductionTumor MicroenvironmentAntineoplastic AgentsReceptors, Tumor Necrosis Factor, Type IITNFRSF1B protein, humanimmunosuppressiveimmunotherapynanoparticlesregulatory T cellsTNF

Identifiers

PMID31877663
PMCPMC7016661
OpenAlexW2995715934

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.