Evidence map›Paper›PMID 37603104›Full record

ArticleJournal of cancer research and clinical oncology2023

A novel LINC00478 serves as a tumor suppressor in endometrial carcinoma progression.

Yingyi Feng, Yongshun Dong, Boqi Rao, Yonghui Yu, Wenpeng Su, Jie Zeng, Eryong Zhao, Yongxiu Chen, Shenying Fang, Yifeng Zhou and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

12 authors at 4 institutions in 1 country.

Yingyi Feng *State Key Lab of Respiratory Disease, Institute for Chemical Carcinogenesis, Collaborative Innovation Center for Environmental Toxicity, School of Public Health, Guangzhou Medical University, 1 Xinzao Road, Panyu District, Guangzhou, 511436, People's Republic of China.
Yongshun Dong *State Key Lab of Respiratory Disease, Institute for Chemical Carcinogenesis, Collaborative Innovation Center for Environmental Toxicity, School of Public Health, Guangzhou Medical University, 1 Xinzao Road, Panyu District, Guangzhou, 511436, People's Republic of China.
Boqi Rao *State Key Lab of Respiratory Disease, Institute for Chemical Carcinogenesis, Collaborative Innovation Center for Environmental Toxicity, School of Public Health, Guangzhou Medical University, 1 Xinzao Road, Panyu District, Guangzhou, 511436, People's Republic of China.
Yonghui YuState Key Lab of Respiratory Disease, Institute for Chemical Carcinogenesis, Collaborative Innovation Center for Environmental Toxicity, School of Public Health, Guangzhou Medical University, 1 Xinzao Road, Panyu District, Guangzhou, 511436, People's Republic of China.
Wenpeng SuState Key Lab of Respiratory Disease, Institute for Chemical Carcinogenesis, Collaborative Innovation Center for Environmental Toxicity, School of Public Health, Guangzhou Medical University, 1 Xinzao Road, Panyu District, Guangzhou, 511436, People's Republic of China.
Jie ZengDepartment of Obstetrics and Gynecology, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Guangzhou, 510150, People's Republic of China.
Eryong ZhaoDepartment of Obstetrics and Gynecology, Guangzhou Women and Children's Medical Center, Guangzhou, 510000, People's Republic of China.
Yongxiu ChenDepartment of Gynaecology and Obstetrics, Guangdong Women's and Children's Hospital, Guangzhou, 511400, People's Republic of China.
Shenying FangThe Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510799, People's Republic of China.
Yifeng ZhouDepartment of Genetics, Medical College of Soochow University, Suzhou, 215123, People's Republic of China.
Jiachun LuState Key Lab of Respiratory Disease, Institute for Chemical Carcinogenesis, Collaborative Innovation Center for Environmental Toxicity, School of Public Health, Guangzhou Medical University, 1 Xinzao Road, Panyu District, Guangzhou, 511436, People's Republic of China.
Fuman QiuState Key Lab of Respiratory Disease, Institute for Chemical Carcinogenesis, Collaborative Innovation Center for Environmental Toxicity, School of Public Health, Guangzhou Medical University, 1 Xinzao Road, Panyu District, Guangzhou, 511436, People's Republic of China. fumanqiu@gzhmu.edu.cn.
Guangzhou Medical University · CNGuangdong Province Women and Children Hospital · CNSoochow University · CNThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

National Natural Science Foundation of China 81602289National Natural Science Foundation of China 81872694National Natural Science Foundation of China 81973111
6 · The paper itself

Abstract

backgroundLong noncoding RNAs (lncRNAs) are involved in the pathogenesis and progression of various cancers, but their roles in endometrial cancer (EC) are largely unknown.

methodsThe expressions of LINC00478 and PTBP1 in EC tissues were determined by RT-qPCR. Cell counting kit-8, flow cytometry and Transwell assays were executed for detecting the roles of LINC00478 in EC cells proliferation, migration and invasion. The mouse-xenograft models were established by subcutaneous injection in vivo. The interaction between LINC00478 and PTBP1 was confirmed by RNA pull-down assay and RNA-binding protein immunoprecipitation assay.

resultsLINC00478 was significantly down-regulated in EC tissues while compared to that in their paracancerous samples, and a higher expression level of LINC00478 was negatively correlated with clinical progress of EC patients. Functional experiments in vivo and in vitro revealed that LINC00478 overexpression could dramatically retard the proliferation of EC cells, decrease the rate of colony formation, suppress the migration and invasion abilities of EC cells in vitro and inhibit tumor growth in vivo. Mechanistically, LINC00478 regulated the expression of PTBP1, a key factor in the Warburg effect, and affected the metabolic process of EC cells.

conclusionsLINC00478 acts as a tumor suppressor in EC by negatively controlling PTBP1 expression and influencing the Warburg effect, providing a potential biomarker and therapeutic target for patients with EC.

Indexed as

Endometrial NeoplasmsMicroRNAsRNA, Long NoncodingAnimalsCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHeterogeneous-Nuclear RibonucleoproteinsHumansMicePolypyrimidine Tract-Binding ProteinHeterogeneous-Nuclear RibonucleoproteinsMicroRNAsPolypyrimidine Tract-Binding ProteinPTBP1 protein, humanRNA, Long NoncodingEndometrial cancerLINC00478PTBP1Warburg effect

Identifiers

PMID37603104
PMCPMC11796644
OpenAlexW4386019927

What OpenQuestion holds

Textmetadata
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.