Evidence map›Paper›PMID 33199829›Full record

ArticleCancer gene therapy2021

Silencing of long non-coding RNA LINC01270 inhibits esophageal cancer progression and enhances chemosensitivity to 5-fluorouracil by mediating GSTP1methylation.

Nuo Li, Zhifeng Zhao, Feng Miao, Shuang Cai, Pengliang Liu, Yang Yu, Baoming Wang

Erratum issuedAbstract read
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In one paragraph

Article in Cancer gene therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

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  15. LncRNA-mediated DNA methylation: an emerging mechanism in cancer and beyond.Journal of experimental & clinical cancer research : CR · 2022
    Review
  16. Article
  17. Non-coding RNA-mediated high expression ofFrontiers in immunology · 2022
    Article
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  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Nuo LiDepartment of Gastroenterology, The Fourth Affiliated Hospital of China Medical University, 110032, Shenyang, P.R. China.
Zhifeng ZhaoDepartment of Gastroenterology, The Fourth Affiliated Hospital of China Medical University, 110032, Shenyang, P.R. China.
Feng MiaoDepartment of Gastroenterology, The Fourth Affiliated Hospital of China Medical University, 110032, Shenyang, P.R. China.
Shuang CaiDepartment of Gastroenterology, The Fourth Affiliated Hospital of China Medical University, 110032, Shenyang, P.R. China.
Pengliang LiuDepartment of Gastroenterology, The Fourth Affiliated Hospital of China Medical University, 110032, Shenyang, P.R. China.
Yang YuDepartment of Gastroenterology, The Fourth Affiliated Hospital of China Medical University, 110032, Shenyang, P.R. China.
Baoming WangDepartment of Intervention, The Fourth Affiliated Hospital of China Medical University, 110032, Shenyang, P.R. China. wangbaoming1976@126.com.ORCID http://orcid.org/0000-0001-8818-5860
Fourth Affiliated Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Esophageal cancer (EC) is a serious digestive malignancy which remains the sixth leading cause of cancer-related deaths worldwide. Emerging evidence suggests the involvement of long non-coding RNAs (lncRNAs) in the tumorigenesis of EC and thus, in this study we explored the potential effects of lncRNA LINC01270 on EC cell proliferation, migration, invasion and, drug resistance via regulation of glutathione S-transferase P1 (GSTP1) methylation. First, we screened out the EC-related differentially expressed lncRNAs, and the expression of our top candidate LINC01270 was quantified in EC tissues and cells. To define the role of LINC01270 in EC progression, we evaluated the proliferation, migration and invasion of EC cells when the LINC01270 was overexpressed or knocked down, in the presence of the GSTP1 methylation inhibitor SGI-1027 and 5-fluorouracil (5-FU). In addition, interaction between LINC01270 and methylation of the GSTP1 promoter was identified. Finally, we assessed transplantable tumor growth in nude mice. LINC01270 was up-regulated and GSTP1 was down-regulated in EC tissues and cells. Silencing of LINC01270 inhibited migration and invasion, and enhanced the sensitivity of 5-FU in EC cells. We found that LINC01270 recruited the DNA methyltransferases DNMT1, DNMT3A and DNMT3B initiating GSTP1 promoter methylation, thereby leading to the proliferation, migration, invasion and drug resistance of EC cells. Moreover, GSTP1 overexpression was observed to reverse the effects of LINC01270 overexpression on EC cells and their response to 5-FU. Taken together, this study shows that inhibition of LINC01270 can lead to suppression of EC progression via demethylation of GSTP1, highlighting this lncRNA as a potential target for EC treatment.

Indexed as

DNA MethylationDrug Resistance, NeoplasmAdultAgedAnimalsAntimetabolites, AntineoplasticApoptosisCell MovementCell ProliferationEsophageal NeoplasmsFemaleFluorouracilGene Expression Regulation, NeoplasticGene SilencingGlutathione S-Transferase piHumansAntimetabolites, AntineoplasticFluorouracilGlutathione S-Transferase piGSTP1 protein, humanRNA, Long Noncoding

Identifiers

PMID33199829
OpenAlexW3099843425

What OpenQuestion holds

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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.