Evidence map›Paper›PMID 31317661›Full record

ArticleThoracic cancer2019

Silencing of RAD51AP1 suppresses epithelial-mesenchymal transition and metastasis in non-small cell lung cancer.

Yuanyuan Wu, Huifeng Wang, Lijiao Qiao, Xiangming Jin, Hui Dong, Yan Wang

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  5. [Research Advances of RAD51AP1 in Tumor Progression and Drug Resistance].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Review
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  7. International journal of general medicine · 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

6 authors at 1 institution in 1 country.

Yuanyuan WuDepartment of Oncology, Cancer Hospital, General Hospital of Ningxia Medical University, Yinchuan, China.
Huifeng WangDepartment of Oncology, Cancer Hospital, General Hospital of Ningxia Medical University, Yinchuan, China.
Lijiao QiaoDepartment of Oncology, Cancer Hospital, General Hospital of Ningxia Medical University, Yinchuan, China.
Xiangming JinDepartment of Oncology, Cancer Hospital, General Hospital of Ningxia Medical University, Yinchuan, China.
Hui DongCenter of Research Equipment Management, General Hospital of Ningxia Medical University, Yinchuan, China.ORCID 0000-0002-8463-2413
Yan WangDepartment of Oncology, Cancer Hospital, General Hospital of Ningxia Medical University, Yinchuan, China.
Ningxia Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-small cell lung cancer (NSCLC) is a major cause of cancer-related mortality and is frequently accompanied by metastasis. The crucial roles of genes in lung cancer have attracted attention. Thus, this study aimed to investigate the effects of RAD51AP1 on the epithelial-mesenchymal transition (EMT) and metastasis of NSCLC.

methodsThe positive expression rate of the RAD51AP1 protein was examined. NSCLC cells were transfected with a series of plasmids to alter the expression of RAD51AP1 to clarify the influence of RAD51AP1 on EMT and metastasis in NSCLC, as well as NSCLC cell migration, invasion, apoptosis, proliferation, and cloning. An in vivo experiment was conducted to determine the oncogenicity of human NSCLC cells in nude mice.

resultsRAD51AP1 was highly expressed in NSCLC tissues. Furthermore, we found promotion of N-cadherin, vimentin, fibronectin, MMP-2, OPN, CD62, and TMP-2, but inhibition of E-cadherin, occludin, cytokeratin in the context of elevated RAD51AP1 expression. An in vivo experiment also confirmed that silencing of RAD51AP1 could inhibit NSCLC tumor formation and growth.

conclusionOur results revealed that RAD51AP1 silencing suppressed the EMT and metastasis of NSCLC, thereby highlighting its potential as a promising novel target for NSCLC treatment.

Indexed as

Epithelial-Mesenchymal TransitionAnimalsApoptosisBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell MovementCell ProliferationDNA-Binding ProteinsFemaleFollow-Up StudiesHumansLung NeoplasmsMaleMiceMice, NudeMiddle AgedBiomarkers, TumorDNA-Binding ProteinsRAD51AP1 protein, humanRNA-Binding ProteinsRNA, Small InterferingEpithelial-mesenchymal transitioninvasionmetastasisnon-small cell lung cancerRAD51 associated protein 1

Identifiers

PMID31317661
PMCPMC6718026
OpenAlexW2964316964

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.