Evidence map›Paper›PMID 34188249›Full record

ReviewOncogene2021

B cell heterogeneity, plasticity, and functional diversity in cancer microenvironments.

Yuan Wei, Chun-Xiang Huang, Xiao Xiao, Dong-Ping Chen, Hong Shan, Huanhuan He, Dong-Ming Kuang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.7field-weighted citation impact, top 7% 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

33 citing papers in PubMed, 45 citations in OpenAlex.

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  19. miRNome targeting NF-κB signaling orchestrates macrophage-triggered cancer metastasis and recurrence.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
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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

7 authors at 2 institutions in 2 countries.

Yuan WeiThe Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China.ORCID http://orcid.org/0000-0001-5694-8835
Chun-Xiang HuangMOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Xiao XiaoCancer Program, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Dong-Ping ChenMOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Hong ShanThe Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China. shanhong@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0001-6640-1390
Huanhuan HeThe Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China. hehh23@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-5903-0840
Dong-Ming KuangThe Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China. kdming@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0003-3570-9717
Sun Yat-sen University · CNQIMR Berghofer Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B cells constitute a major component of tumor-infiltrating leukocytes. However, the influence of these cells on malignancy is currently under debate, reflecting the heterogeneity of B cell subsets in tumors. With recent advances, it becomes apparent that this debate includes not only the evaluation of B cells themselves, but also the underlying immune microenvironment network, which scripts the highly heterogeneous B cell populations in tumors and directs the roles of those sub-populations in disease progression and clinical treatment. In this review, we summarize recent findings on the heterogeneous subset composition of B cells in both human and mouse tumor models and their different impacts on disease progression. We further describe the multidimensional interplays between B cells and other immune cells in the tumor microenvironment, which account for the regulation of B cell differentiation and function in situ. We also assess the potential influences of distinct sub-tumor locations on B cell function in primary tumors during development and those under immunotherapy treatment. Illuminating the heterogeneous nature of B cell subset composition, generation, localization, and related immune network in tumor is of immense significance for comprehensively understanding B cell response in tumor and designing more efficacious cancer immunotherapies.

Indexed as

NeoplasmsTumor MicroenvironmentAnimalsB-LymphocytesB-Lymphocyte SubsetsCell DifferentiationCell PlasticityHumansImmunotherapyLymphocytes, Tumor-InfiltratingMice

Identifiers

PMID34188249
OpenAlexW3175963836

What OpenQuestion holds

Textmetadata
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.