Evidence map›Paper›PMID 37231545›Full record

ArticleThoracic cancer2023

A novel molecular mechanism mediated by circCCDC134 regulates non-small cell lung cancer progression.

Zhufeng Tong, Zhen Wang, Jinghan Jiang, Chengcheng Tong, Lan Wu

Abstract 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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. CircRNA Regulation of T Cells in Cancer: Unraveling Potential Targets.International journal of molecular sciences · 2024
    Review
  8. Review
  9. Article
  10. Role of circular RNAs in lung cancer.Frontiers in genetics · 2024
    Review
  11. Review
  12. Article
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.

Zhufeng TongDepartment of General Practice, The First Affiliated Hospital of Wannan Medical College, Wuhu, People's Republic of China.
Zhen WangDepartment of General Practice, The First Affiliated Hospital of Wannan Medical College, Wuhu, People's Republic of China.
Jinghan JiangDepartment of General Practice, The First Affiliated Hospital of Wannan Medical College, Wuhu, People's Republic of China.
Chengcheng TongDepartment of General Practice, The First Affiliated Hospital of Wannan Medical College, Wuhu, People's Republic of China.
Lan WuHealth management center, The First Affiliated Hospital of Wannan Medical College, Wuhu, People's Republic of China.ORCID 0009-0005-1890-5697

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCircular RNA (circRNA) plays a crucial role in non-small cell lung cancer (NSCLC) progression. However, the role of circCCDC134 in NSCLC is still largely unknown.

methodsQuantitative real-time PCR was utilized for measuring circCCDC134, microRNA (miR)-625-5p and nuclear factor of activated T cell 5 (NFAT5) expression. Cell functions were evaluated by colony formation, EdU, transwell, and wound healing assays and flow cytometry. Glucose consumption, lactate production, and ATP level were determined to analyze cell glycolysis. Western blot analysis was used to detect protein expression. Animal experiments were performed to assess the effect of circCCDC134 on NSCLC tumor growth. RNA interaction was evaluated by dual-luciferase reporter assay and RIP assay. Exosomes were isolated from the serum of NSCLC patients and healthy normal controls.

resultsHighly expressed circCCDC134 was found in NSCLC tissues and cells, as well as in the serum exosomes of NSCLC patients. Downregulated circCCDC134 restrained NSCLC cell growth, metastasis and glycolysis. CircCCDC134 sponged miR-625-5p to regulate NFAT5. MiR-625-5p inhibitor abolished the regulation of circCCDC134 knockdown on NSCLC progression, and NFAT5 overexpression eliminated the effects of miR-625-5p on NSCLC cell behaviors. CircCCDC134 knockdown also inhibited NSCLC tumor growth.

conclusionOur study revealed that circCCDC134 was involved in regulating NSCLC progression through the miR-625-5p/NFAT5 pathway, confirming that circCCDC134 might function as the diagnostic and therapeutic target for NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungExosomesLung NeoplasmsMicroRNAsAnimalsCell ProliferationHumansLactic AcidLactic AcidMicroRNAsMIRN625 microRNA, humancircCCDC134miR-625-5pNFAT5non-small cell lung cancer

Identifiers

PMID37231545
PMCPMC10344740

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.