Evidence map›Paper›PMID 28241765›Full record

ReviewJournal of translational medicine2017

Heterogeneity of Toll-like receptor 9 signaling in B cell malignancies and its potential therapeutic application.

Ling Bai, Wei Chen, Jingtao Chen, Wei Li, Lei Zhou, Chao Niu, Wei Han, Jiuwei Cui

Open access · goldAbstract readReview
In one paragraph

Review in Journal of translational medicine, 2017. 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
1.3field-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, 30 citations in OpenAlex.

  1. Review
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  8. Targeted In Vivo Delivery of NF-κB Decoy Inhibitor Augments Sensitivity of B Cell Lymphoma to Therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
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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 2 institutions in 2 countries.

Ling BaiCancer Center, The First Bethune Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Wei ChenADC Biomedical Research Institute, 1919 University Avenue, Saint Paul, MN, 55104, USA.
Jingtao ChenInstitute of Translational Medicine, The First Bethune Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Wei LiCancer Center, The First Bethune Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Lei ZhouCancer Center, The First Bethune Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Chao NiuCancer Center, The First Bethune Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Wei HanCancer Center, The First Bethune Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Jiuwei CuiCancer Center, The First Bethune Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China. cuijw@jlu.edu.cn.
First Bethune Hospital of Jilin University · CNBiomedical Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptor 9 (TLR9) is expressed in a variety of B-cell malignancies and works as a bridge between innate and adaptive immunity. CpG oligodeoxynucleotides (CpG ODNs), TLR9 agonists, are able to induce anticancer immune responses and exert direct effects against cancer cells, serving as cancer therapeutic agents. Therefore, TLR9 might be a potential therapeutic target for drug development. However, several new evidences have revealed that direct effects of TLR9 agonists on B-cell malignancies is controversial. For example, CpG ODNs can induce apoptosis in certain type of chronic lymphocytic leukemia and lymphoma cells, while induce proliferation in multiple myeloma and other types of lymphoma cells. In this review, we summarize current understanding of the heterogeneity in responses of normal and malignant B cells to TLR9 agonists, due to differences in TLR9 expression levels, genetic alterations (such as MyD88 mutation), and signaling pathway activation. Especially, the downstream molecules of NF-κB signaling pathway play an important role in the heterogeneous response. In order to provide possibilities for therapeutic manipulation of TLR9 agonists in the treatment of these disorders, the preclinical and clinical advances in using CpG ODNs alone and in combination therapies are also summarized in this review.

Indexed as

Signal TransductionAnimalsHumansLeukemia, B-CellLymphocyte SubsetsModels, BiologicalOligodeoxyribonucleotidesToll-Like Receptor 9CPG-oligonucleotideOligodeoxyribonucleotidesToll-Like Receptor 9B-cell malignanciesCancer immunotherapyCpG oligodeoxynucleotidesToll-like receptor 9

Identifiers

PMID28241765
PMCPMC5329966
OpenAlexW2591575696

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.