Evidence map›Paper›PMID 39215037›Full record

ArticleNPJ precision oncology2024

M2 macrophage-derived lncRNA NORAD in EVs promotes NSCLC progression via miR-520g-3p/SMIM22/GALE axis.

Qingtao Zhao, Bin Li, Xiaopeng Zhang, Huanfen Zhao, Wenfei Xue, Zheng Yuan, Shun Xu, Guochen Duan

Abstract read
In one paragraph

Article in NPJ precision oncology, 2024. 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
–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

13 citing papers in PubMed.

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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.

Qingtao Zhao *Department of Thoracic Surgery, Hebei General Hospital, Shijiazhuang, Hebei Province, China.ORCID http://orcid.org/0000-0001-6400-2329
Bin Li *Hebei Bio-High Technology Development Co.Ltd, Shijiazhuang, Hebei Province, China.ORCID http://orcid.org/0000-0002-9433-5543
Xiaopeng ZhangDepartment of Thoracic Surgery, Hebei General Hospital, Shijiazhuang, Hebei Province, China.
Huanfen ZhaoDepartment of Pathology, Hebei General Hospital, Shijiazhuang, Hebei Province, China.
Wenfei XueDepartment of Thoracic Surgery, Hebei General Hospital, Shijiazhuang, Hebei Province, China.
Zheng YuanDepartment of Nursing, Hebei General Hospital, Shijiazhuang, Hebei Province, China.
Shun XuDepartment of Thoracic Surgery, The First Hospital of China Medical University, Shenyang, Liaoning, China. xushuncmu@sina.com.ORCID http://orcid.org/0009-0001-1374-5322
Guochen DuanDepartment of Thoracic Surgery, Hebei General Hospital, Shijiazhuang, Hebei Province, China. duanguoc@126.com.ORCID http://orcid.org/0000-0001-9608-4066

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) constitutes the majority of lung cancer cases, accounting for over 80%. RNAs in EVs play a pivotal role in various biological and pathological processes mediated by extracellular vesicle (EV). Long non-coding RNAs (lncRNAs) are widely associated with cancer-related functions, including cell proliferation, migration, invasion, and drug resistance. Tumor-associated macrophages are recognized as pivotal contributors to tumorigenesis. Given these insights, this study aims to uncover the impact of lncRNA NORAD in EVs derived from M2 macrophages in NSCLC cell lines and xenograft mouse models of NSCLC. EVs were meticulously isolated and verified based on their morphology and specific biomarkers. The interaction between lncRNA NORAD and SMIM22 was investigated using immunoprecipitation. The influence of SMIM22/GALE or lncRNA NORAD in EVs on glycolysis was assessed in NSCLC cell lines. Additionally, we evaluated the effects of M2 macrophage-derived lncRNA NORAD in EVs on cell proliferation and apoptosis through colony formation and flow cytometry assays. Furthermore, the impact of M2 macrophage-derived lncRNA NORAD in EVs on tumor growth was confirmed using xenograft tumor animal models. The results underscored the potential role of M2 macrophage-derived lncRNA NORAD in EVs in NSCLC. SMIM22/GALE promoted glycolysis and the proliferation of NSCLC cells. Furthermore, lncRNA NORAD in EVs targeted SMIM22 and miR-520g-3p in NSCLC cells. Notably, lncRNA NORAD in EVs promoted the proliferation of NSCLC cells and facilitated NSCLC tumor growth through the miR-520g-3p axis. In conclusion, M2 macrophage-derived lncRNA NORAD in EVs promotes NSCLC progression through the miR-520g-3p/SMIM22/GALE axis.

Identifiers

PMID39215037
PMCPMC11364787

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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.