Evidence map›Paper›PMID 35050556›Full record

ArticleThe Kaohsiung journal of medical sciences2022

microRNA-1321 and microRNA-7515 contribute to the progression of non-small cell lung cancer by targeting CDC20.

Hao Hu, Fang-Fang Tou, Wei-Min Mao, Yan-Liang Xu, Hui Jin, Yu-Kang Kuang, Chun-Bin Han, Chang-Ying Guo

Open access · goldAbstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2022. 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
1.1field-weighted citation impact, top 24% 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, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. CDC20: a novel therapeutic target in cancer.American journal of translational research · 2023
    Review
  7. 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

8 authors at 4 institutions in 2 countries.

Hao HuDepartment of Thoracic Surgery, Jiangxi Cancer Hospital, Nanchang, China.
Fang-Fang TouDepartment of Thoracic Surgery, Jiangxi Cancer Hospital, Nanchang, China.
Wei-Min MaoDepartment of Thoracic Surgery, Jiangxi Cancer Hospital, Nanchang, China.
Yan-Liang XuDepartment of Thoracic Surgery, Jiangxi Cancer Hospital, Nanchang, China.
Hui JinDepartment of Thoracic Surgery, Ji'an Central Hospital, Ji'an, China.
Yu-Kang KuangDepartment of Thoracic Surgery, Jiangxi Cancer Hospital, Nanchang, China.
Chun-Bin HanDepartment of Thoracic Surgery, Jiangxi Cancer Hospital, Nanchang, China.
Chang-Ying GuoDepartment of Thoracic Surgery, Jiangxi Cancer Hospital, Nanchang, China.ORCID https://orcid.org/0000-0001-7167-5441
Jiangxi Provincial Cancer Hospital · CNChinese General Hospital College of Nursing and Liberal Arts · PHFirst Hospital of Xi'an · CNNanchang University · CN

Funding

Key Research and Development Projects in Jiangxi Province 20203BBGL73151National Natural Science Foundation of China 81560382
6 · The paper itself

Abstract

Cell division cycle 20 (CDC20) and microRNAs (miRNAs) are differentially expressed in non-small cell lung cancer (NSCLC). The current study aimed to investigate the role of miR-1321 and miR-7515 regulation in CDC20 during NSCLC development. CDC20 expression in paracancerous and tumor tissues was assessed using quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The relationship between CDC20 expression and prognosis of patients was analyzed using the TCGA database. The expression profile of CDC20 in healthy lung cells and NSCLC cells was detected using qRT-PCR and western blotting. After the knockdown of CDC20 in NSCLC cells, the cell proliferation, apoptosis, migration, invasion, and cell cycle changes were investigated by CCK8, EdU, flow cytometry, wound healing, and Transwell assays. The miRNAs targeting CDC20 were predicted using two bioinformatics websites and validated using dual-luciferase assays. CDC20 was enhanced in NSCLC tissues and cells, thus predicting the poor prognosis in NSCLC patients. After CDC20 inhibition, the malignant phenotype of NSCLC cells was reverted. miR-1321 and miR-7515 targeted CDC20 and exhibited the same anti-tumor effects as CDC20 silencing. Functional rescue experiments showed that CDC20 overexpression averted the anti-tumor effects of miR-1321 and miR-7515 on NSCLC cells. miR-1321 and miR-7515 inhibited NSCLC development by targeting CDC20. Thus, the current study has implications in NSCLC treatment and provides novel insights into NSCLC management.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMicroRNAsApoptosisCdc20 ProteinsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansCDC20 protein, humanCdc20 ProteinsMicroRNAsCDC20microRNA-1321microRNA-7515non-small cell lung cancerproliferation

Identifiers

PMID35050556
PMCPMC11896554
OpenAlexW4205920215

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.