Evidence map›Paper›PMID 38733179›Full record

ArticleCancer medicine2024

Long non-coding RNA NEAT1 promotes aerobic glycolysis and progression of cervical cancer through WNT/β-catenin/PDK1 axis.

Min Su, Ziyan Liang, Shidong Shan, Yang Gao, Li He, Xuelian Liu, Anjin Wang, Hua Wang, Hongbing Cai

Abstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

9 authors.

Min SuDepartment of Gynecological Oncology, Zhongnan Hospital, Wuhan University, Wuhan, People's Republic of China.ORCID 0000-0002-4999-2886
Ziyan LiangDepartment of Gynecological Oncology, Zhongnan Hospital, Wuhan University, Wuhan, People's Republic of China.
Shidong ShanHubei Key Laboratory of Tumor Biological Behaviors, Wuhan, People's Republic of China.
Yang GaoDepartment of Gynecological Oncology, Zhongnan Hospital, Wuhan University, Wuhan, People's Republic of China.
Li HeHubei Key Laboratory of Tumor Biological Behaviors, Wuhan, People's Republic of China.
Xuelian LiuDepartment of Gynecological Oncology, Zhongnan Hospital, Wuhan University, Wuhan, People's Republic of China.
Anjin WangDepartment of Gynecological Oncology, Zhongnan Hospital, Wuhan University, Wuhan, People's Republic of China.
Hua WangDepartment of Gynecological Oncology, Zhongnan Hospital, Wuhan University, Wuhan, People's Republic of China.
Hongbing CaiDepartment of Gynecological Oncology, Zhongnan Hospital, Wuhan University, Wuhan, People's Republic of China.

Funding

National Natural Science Foundation of China 81972447
6 · The paper itself

Abstract

backgroundCervical cancer is one of the most common gynecological cancers. Accumulated evidence shows that long non-coding RNAs (lncRNAs) play essential roles in cervical cancer occurrence and progression, but their specific functions and mechanisms remain to be further explored.

methodsThe RT-qPCR assay was used to detect the expression of NEAT1 in cervical cancer tissues and cell lines. CCK-8, colony formation, flow cytometry, western blotting, and Transwell assays were used to evaluate the impact of NEAT1 on the malignant behavior of cervical cancer cells. Glucose consumption, lactate production, ATP levels, ROS levels, MMP levels, and the mRNA expressions of glycolysis-related genes and tricarboxylic acid cycle-related genes were detected to analyze the effect of NEAT1 on metabolism reprograming in cervical cancer cells. The expressions of PDK1, β-catenin and downstream molecules of the WNT/β-catenin signaling pathway in cervical cancer cells and tissues were detected by western blotting, RT-qPCR, immunofluorescence and immunohistochemistry assays.

resultsThis study investigated the role and possible molecular mechanism of lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1) in cervical cancer. Our results showed that NEAT1 was highly expressed in cervical cancer tissues and cell lines. Downregulation of NEAT1 inhibited the proliferation, migration, invasion and glycolysis of cervical cancer cells, while overexpression of NEAT1 led to the opposite effects. Mechanistically, NEAT1 upregulated pyruvate dehydrogenase kinase (PDK1) through the WNT/β-catenin signaling pathway, which enhanced glycolysis and then facilitated cervical cancer metastasis. Furthermore, NEAT1 maintained the protein stability of β-catenin but did not affect its mRNA level. We also excluded the direct binding of NEAT1 to the β-catenin protein via RNA pull-down assay. The suppressive impact of NEAT1 knockdown on cell proliferation, invasion, and migration was rescued by β-catenin overexpression. The WNT inhibitor iCRT3 attenuated the carcinogenic effect induced by NEAT1 overexpression.

conclusionIn summary, these findings indicated that NEAT1 may contribute to the progression of cervical cancer by activating the WNT/β-catenin/PDK1 signaling axis.

Indexed as

Cell ProliferationDisease ProgressionGene Expression Regulation, NeoplasticPyruvate Dehydrogenase Acetyl-Transferring KinaseRNA, Long NoncodingUterine Cervical NeoplasmsWnt Signaling Pathwaybeta CateninCell Line, TumorCell MovementFemaleGlycolysisHumansbeta CateninCTNNB1 protein, humanNEAT1 long non-coding RNA, humanPDK1 protein, humanPyruvate Dehydrogenase Acetyl-Transferring KinaseRNA, Long Noncodingcervical cancerglycolysisNEAT1PDK1WNT/β‐catenin

Identifiers

PMID38733179
PMCPMC11087816

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.