Evidence map›Paper›PMID 36262998›Full record

ArticleContrast media & molecular imaging2022

Knockdown of Long Noncoding RNA LINC00240 Inhibits Esophageal Cancer Progression by Regulating miR-26a-5p.

Yupeng Liu, Tao Li, Chunlei Peng, Qinghua Mao, Biao Shen, Minxin Shi, Haimin Lu, Ting Xiao, Aimin Yang, Chun Cheng

Open access · hybridAbstract read
In one paragraph

Article in Contrast media & molecular imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

4 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
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  4. Review
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

10 authors at 1 institution in 1 country.

Yupeng LiuDepartment of Thoracic Surgery, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Tao LiDepartment of Medical Oncology, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Chunlei PengDepartment of Medical Oncology, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Qinghua MaoDepartment of Thoracic Surgery, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Biao ShenDepartment of Thoracic Surgery, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Minxin ShiDepartment of Thoracic Surgery, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Haimin LuDepartment of Thoracic Surgery, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Ting XiaoDepartment of Thoracic Surgery, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Aimin YangDepartment of Thoracic Surgery, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.
Chun ChengDepartment of Thoracic Surgery, Tumor Hospital Affiliated to Nantong University, Nantong 226000, China.ORCID 0000-0002-5096-0099
Nantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Esophageal cancer is the most prevalent digestive system tumor. Due to a lack of characteristic symptoms and early diagnosis, a confirmed esophageal cancer is typically detected at a progressively harmful stage. Therefore, it is critical to investigate the molecular mechanisms governing the formation and progression of esophageal cancer in order to identify new treatment targets for esophageal cancer early detection. Methods: We first screened the differentially expressed gene LINC00240 in the TCGA database. Multivariate analysis and Cox regression were performed, and a nomogram was constructed for internal validation. The correlation between LINC00240 and immune cells was analyzed using the TIMER database. The possible mechanism of action was explored through GSEA enrichment analysis. Then, in 43 esophageal cancer tissues, paracancour tissues, and cell lines, the LINC00240 expression was found. Transwell assays, CCK-8, and clone formation assays were utilized to assess the impact of LINC00240 on the metastasis of esophageal cancer cells. The binding activity of LINC00240 to downstream miRNAs was assessed using the luciferase reporter gene. Results: TCGA database showed that LINC00240 expression was increased in cancer tissues compared to adjacent tissues. The Conclusion: LINC00240 expression is elevated in esophageal cancerous tissues, and knocking down LINC00240 decreases esophageal cancer cell proliferation, clone formation, invasion, and migration via miR-26a-5p. As a result, LINC00240 could be a novel target for esophageal cancer patients' early diagnosis and treatment.

Indexed as

Esophageal NeoplasmsMicroRNAsRNA, Long NoncodingCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansSincalideMicroRNAsMIRN26 microRNA, humanRNA, Long NoncodingSincalide

Identifiers

PMID36262998
PMCPMC9556215
OpenAlexW4302024633

What OpenQuestion holds

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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.