Evidence map›Paper›PMID 28627514›Full record

ArticleNature communications2017

Simultaneous overactivation of Wnt/β-catenin and TGFβ signalling by miR-128-3p confers chemoresistance-associated metastasis in NSCLC.

Junchao Cai, Lishan Fang, Yongbo Huang, Rong Li, Xiaonan Xu, Zhihuang Hu, Le Zhang, Yi Yang, Xun Zhu, Heng Zhang and 8 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 116 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 1 pooled it
7.6field-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

116 citing papers in PubMed, 1 synthesis or guideline pooled it, 199 citations in OpenAlex.

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56 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 2 countries.

Junchao CaiDepartment of Microbiology, Sun Yat-sen University Zhongshan School of Medicine, Guangzhou 510080, China.
Lishan FangDepartment of Microbiology, Sun Yat-sen University Zhongshan School of Medicine, Guangzhou 510080, China.
Yongbo HuangState Key Laboratory of Respiratory Diseases and Guangzhou Institute of Respiratory Diseases, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Rong LiDepartment of Microbiology, Sun Yat-sen University Zhongshan School of Medicine, Guangzhou 510080, China.
Xiaonan XuDepartment of Microbiology, Sun Yat-sen University Zhongshan School of Medicine, Guangzhou 510080, China.
Zhihuang HuDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Le ZhangDepartment of Microbiology, Sun Yat-sen University Zhongshan School of Medicine, Guangzhou 510080, China.
Yi YangDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Xun ZhuDepartment of Microbiology, Sun Yat-sen University Zhongshan School of Medicine, Guangzhou 510080, China.
Heng ZhangNeurosurgery Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China.
Jueheng WuKey Laboratory of Tropical Disease Control (Sun Yat-sen University), Ministry of Education, Guangzhou 510080, China.
Yan HuangDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Jun LiDepartment of Biochemistry, Sun Yat-sen University Zhongshan School of Medicine, Guangzhou 510080, China.
Musheng ZengState Key Laboratory of Oncology in South China, Department of Experimental Research, Sun Yat-Sen University Cancer Center, Guangzhou 510060, China.
Erwei SongDepartment of Breast Surgery, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou 510120, China.
Yukai HeDepartment of Medicine and Department of Biochemistry and Molecular Biology, Georgia Cancer Center, Augusta University, Augusta, Georgia 30912, USA.
Li ZhangDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Mengfeng LiDepartment of Microbiology, Sun Yat-sen University Zhongshan School of Medicine, Guangzhou 510080, China.
Sun Yat-sen University · CNFudan University Shanghai Cancer Center · CNAugusta University Health · USEighth Affiliated Hospital of Sun Yat-sen UniversityFirst Affiliated Hospital of Guangzhou Medical University · CNSun Yat-sen Memorial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer chemoresistance and metastasis are tightly associated features. However, whether they share common molecular mechanisms and thus can be targeted with one common strategy remain unclear in non-small cell lung cancer (NSCLC). Here, we report that high levels of microRNA-128-3p (miR-128-3p) is key to concomitant development of chemoresistance and metastasis in residual NSCLC cells having survived repeated chemotherapy and correlates with chemoresistance, aggressiveness and poor prognosis in NSCLC patients. Mechanistically, miR-128-3p induces mesenchymal and stemness-like properties through downregulating multiple inhibitors of Wnt/β-catenin and TGF-β pathways, leading to their overactivation. Importantly, antagonism of miR-128-3p potently reverses metastasis and chemoresistance of highly malignant NSCLC cells, which could be completely reversed by restoring Wnt/β-catenin and TGF-β activities. Notably, correlations among miR-128-3p levels, activated β-catenin and TGF-β signalling, and pro-epithelial-to-mesenchymal transition/pro-metastatic protein levels are validated in NSCLC patient specimens. These findings suggest that miR-128-3p might be a potential target against both metastasis and chemoresistance in NSCLC.

Indexed as

Animalsbeta CateninCarcinoma, Non-Small-Cell LungCell Line, TumorDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMice, Inbred BALB CMicroRNAsMiddle AgedSignal TransductionTransforming Growth Factor betabeta CateninCTNNB1 protein, humanMicroRNAsMIRN128 microRNA, humanTransforming Growth Factor beta

Identifiers

PMID28627514
PMCPMC5481840
OpenAlexW2625859437

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.