Evidence map›Paper›PMID 34586722›Full record

ArticleClinical and translational medicine2021

Tumor-derived exosomal miR-19b-3p facilitates M2 macrophage polarization and exosomal LINC00273 secretion to promote lung adenocarcinoma metastasis via Hippo pathway.

Jing Chen, Kai Zhang, Yingru Zhi, Yin Wu, Baoan Chen, Jinyu Bai, Xuerong Wang

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 143 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
143citing papers in PubMed, 2 pooled it
12.4field-weighted citation impact, top 1% 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

143 citing papers in PubMed, 2 syntheses or guidelines pooled it, 197 citations in OpenAlex.

  1. Pooled it
  2. Exosomes in pathogenesis, diagnosis, and therapy of ischemic stroke.Frontiers in bioengineering and biotechnology · 2022
    Pooled it
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83 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Jing ChenDepartment of Hematology and Oncology, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, Jiangsu, P. R. China.
Kai ZhangDepartment of Respiratory Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu, P. R. China.
Yingru ZhiDepartment of Gastroenterology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu, P. R. China.
Yin WuDepartment of Respiratory, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, P. R. China.
Baoan ChenDepartment of Hematology and Oncology, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, Jiangsu, P. R. China.
Jinyu BaiDepartment of Orthopedics, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, P. R. China.
Xuerong WangDepartment of Pharmacology, Nanjing Medical University, Nanjing, Jiangsu, P. R. China.
Zhongda Hospital Southeast University · CNNanjing Medical University · CNSecond Affiliated Hospital of Nanjing Medical University · CNSoochow University · CN

Funding

Advanced PhD research project of the Second Affiliated Hospital of Soochow University SDFEYBS2011National Natural Science Foundation of China 81903089National Natural Science Foundation of China 81903091the Fundamental Research Funds for the Central Universities 2242020R20006the Jiangsu Planned Projects for Postdoctoral Research Funds, and the China Postdoctoral Science Foundation funded project 2020M671534
6 · The paper itself

Abstract

Numerous reports have elucidated the important participation of exosomes in the communication between tumor cells and other cancer-related cells including tumor-associated macrophages (TAMs) in microenvironment. However, the interchange of exosomes between tumor cells and TAMs in the progression of lung adenocarcinoma (LUAD) remains largely enigmatic. Herein, we discovered that LUAD cells induced the M2 polarization of TAMs and the M2-polarized macrophages facilitated LUAD cell invasion and migration and tumor metastasis in vivo. In detail, LUAD cells secreted exosomes to transport miR-19b-3p into TAMs so that miR-19b-3p targeted PTPRD and inhibited the PTPRD-mediated dephosphorylation of STAT3 in TAMs, leading to STAT3 activation and M2 polarization. Also, the activated STAT3 transcriptionally induced LINC00273 in M2 macrophages and exosomal LINC00273 was transferred into LUAD cells. In LUAD cells, LINC00273 recruited NEDD4 to facilitate LATS2 ubiquitination and degradation, so that the Hippo pathway was inactivated and YAP induced the transcription of RBMX. RBMX bound to miR-19b-3p to facilitate the packaging of miR-19b-3p into LUAD cell-derived exosomes. Collectively, our results revealed the mechanism underlying the interactive communication between LUAD cells and TAMs through elucidating the exchange of exosomal miR-19b-3p and LINC00273 and proved the prometastatic effect of the interchange between two cells. These discoveries opened a new vision for developing LUAD treatment.

Indexed as

A549 CellsAdenocarcinoma of LungCell Line, TumorExosomesHippo Signaling PathwayHumansLung NeoplasmsMacrophage ActivationMacrophagesMicroRNAsRNA, Long NoncodingLINC00273 lncRNA, humanMicroRNAsMIRN19A microRNA, humanRNA, Long Noncodingexosomehippo signaling pathwaylung adenocarcinomaM2 macrophage polarizationmiR-19b-3p

Identifiers

PMID34586722
PMCPMC8435259
OpenAlexW3200554002

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LicenceCC BY
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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.