Evidence map›Paper›PMID 37950542›Full record

ArticleThoracic cancer2023

DARS2 promotes the occurrence of lung adenocarcinoma via the ERK/c-Myc signaling pathway.

Tao Fang, Jin Jiang, Wenhao Yu, Rongyang Li, Hui Tian

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-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

7 citing papers in PubMed, 5 citations in OpenAlex.

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  5. Role ofTranslational lung cancer research · 2024
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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

5 authors at 1 institution in 1 country.

Tao FangDepartment of Thoracic Surgery, Qilu Hospital of Shandong University, Jinan, China.
Jin JiangDepartment of Thoracic Surgery, Qilu Hospital of Shandong University, Jinan, China.
Wenhao YuDepartment of Thoracic Surgery, Qilu Hospital of Shandong University, Jinan, China.
Rongyang LiDepartment of Thoracic Surgery, Qilu Hospital of Shandong University, Jinan, China.
Hui TianDepartment of Thoracic Surgery, Qilu Hospital of Shandong University, Jinan, China.ORCID 0000-0002-8932-3003
Shandong University · CN

Funding

National Key Research and Development Program of China 2021YFC2500904National Key Research and Development Program of China 2021YFC2500905Natural Science Foundation of Shandong Province ZR2021LSW006
6 · The paper itself

Abstract

backgroundDARS2 expression is upregulated in lung adenocarcinoma (LUAD) which correlates with tumor patient stage and prognosis. The mechanism of DARS2 involvement in LUAD still needs to be further explored.

methodsIn this study, we found that DARS2 expression in LUAD tissue was significantly higher than that in normal tissue. At the same time, the Kaplan-Meier curve showed that the survival prognosis of LUAD patients with high expression of DARS2 was significantly worse than low expression of DARS2. The expression of DARS2 was detected in LUAD and adjacent normal tissues by IHC staining, histochemical scoring and a survival curve was generated. In addition, we demonstrated that the knockdown and overexpression of DARS2 significantly affected the proliferation, invasion, and migration of LUAD cells in vitro and in vivo. Finally, western blot and rescue assay were performed on LUAD cells to further explore and verify the signaling pathway.

resultsDARS2 expression was significantly upregulated in LUAD tissues and cell lines. What is more, the increased expression of DARS2 was closely related to proliferation, invasion and metastasis. The tumorigenic assay in nude mice further showed that the tumorigenic ability of nude mice was significantly improved with the increase in DARS2 expression. Finally, we determined that DARS2 plays its role in LUAD by targeting the ERK/c-Myc signaling pathway.

conclusionOur data revealed the oncogenic role of DARS2 in LUAD, indicating that DARS2 may be a predictive biomarker and novel therapeutic target for LUAD.

Indexed as

AdenocarcinomaAdenocarcinoma of LungAspartate-tRNA LigaseLung NeoplasmsAnimalsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansMiceMice, NudeProto-Oncogene Proteins c-mycSignal TransductionAspartate-tRNA LigaseDARS2 protein, humanProto-Oncogene Proteins c-mycDARS2ERK/c-Myc signaling pathwaylung adenocarcinoma

Identifiers

PMID37950542
PMCPMC10733159
OpenAlexW4388601197

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.