Evidence map›Paper›PMID 27157642›Full record

ArticleScientific reports2016

miRNA let-7b modulates macrophage polarization and enhances tumor-associated macrophages to promote angiogenesis and mobility in prostate cancer.

Zhigang Wang, Lu Xu, Yinying Hu, Yanqin Huang, Yujuan Zhang, Xiufen Zheng, Shanshan Wang, Yifan Wang, Yanrong Yu, Meng Zhang and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

59 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  14. 17β-estradiol promotes extracellular vesicle release and selective miRNA loading in ERα-positive breast cancer.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

12 authors.

Zhigang WangInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Lu XuInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Yinying HuInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Yanqin HuangInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Yujuan ZhangInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Xiufen ZhengDepartments of Surgery, Pathology, and Oncology, University of Western Ontario, London, Canada.
Shanshan WangInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Yifan WangInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Yanrong YuInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Meng ZhangInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Keng YuanInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.
Weiping MinInstitute of Immunotherapy of Nanchang University, and Jiangxi Academy of Medical Sciences, Nanchang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophage polarization is a highly plastic physiological process that responds to a variety of environmental factors by changing macrophage phenotype and function. Tumor-associated macrophages (TAMs) are generally recognized as promoting tumor progression. As universal regulators, microRNAs (miRNAs) are functionally involved in numerous critical cellular processes including macrophage polarization. Let-7b, a miRNA, has differential expression patterns in inflamed tissues compared with healthy controls. However, whether and how miRNA let-7b regulates macrophage phenotype and function is unclear. In this report, we find that up-regulation of let-7b is characteristic of prostatic TAMs, and down-regulation of let-7b in TAMs leads to changes in expression profiles of inflammatory cytokines, such as IL-12, IL-23, IL-10 and TNF-α. As a result, TAMs treated with let-7b inhibitors reduce angiogenesis and prostate carcinoma (PCa) cell mobility. Let-7b may play a vital role in regulating macrophage polarization, thus modulating the prognosis of prostate cancer.

Indexed as

Cell MovementCell PolarityAntigens, CDCarcinogenesisCell DifferentiationCell Line, TumorCell ProliferationCytokinesDown-RegulationGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsInflammationMacrophagesMaleMicroRNAsAntigens, CDCytokinesMicroRNAsmirnlet7 microRNA, human

Identifiers

PMID27157642
PMCPMC4860600

What OpenQuestion holds

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Registered trials

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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.