Evidence map›Paper›PMID 35166018›Full record

ArticleJournal of cellular and molecular medicine2022

Modulation of lncRNA H19 enhances resveratrol-inhibited cancer cell proliferation and migration by regulating endoplasmic reticulum stress.

Tianye Li, Xinyue Zhang, Linglin Cheng, Chunting Li, Zihan Wu, Yingqi Luo, Kunpeng Zhou, Yanlin Li, Qi Zhao, Yongye Huang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 47 citations in OpenAlex.

  1. International journal of molecular sciences · 2026
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  8. Synergic anti-tumor effects of photodynamic therapy and resveratrol on triple-negative breast cancer cells.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2025
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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

10 authors at 2 institutions in 1 country.

Tianye LiCollege of Life and Health Sciences, Northeastern University, Shenyang, China.
Xinyue ZhangCollege of Life and Health Sciences, Northeastern University, Shenyang, China.
Linglin ChengCollege of Life and Health Sciences, Northeastern University, Shenyang, China.
Chunting LiCollege of Life and Health Sciences, Northeastern University, Shenyang, China.
Zihan WuCollege of Life and Health Sciences, Northeastern University, Shenyang, China.
Yingqi LuoCollege of Life and Health Sciences, Northeastern University, Shenyang, China.
Kunpeng ZhouCollege of Life and Health Sciences, Northeastern University, Shenyang, China.
Yanlin LiCollege of Life and Health Sciences, Northeastern University, Shenyang, China.
Qi ZhaoSchool of Computer Science and Software Engineering, University of Science and Technology Liaoning, Anshan, China.ORCID 0000-0001-9713-1864
Yongye HuangCollege of Life and Health Sciences, Northeastern University, Shenyang, China.ORCID 0000-0002-9083-250X
Northeastern University · CNUniversity of Science and Technology Liaoning · CN

Funding

Fundamental Research Funds for the Central Universities N182004002Fundamental Scientific Research Fund of Liaoning Provincial Education Department LJKQZ2021002National Natural Science Foundation of China 81502582Natural Science Foundation of Liaoning Province 2021-MS-104
6 · The paper itself

Abstract

The phytoalexin resveratrol exhibits anti-tumour activity in many types of cancer. In this study, we showed that resveratrol suppressed the survival of gastric tumour cells both in vivo and in vitro. Resveratrol promoted apoptosis, autophagy and endoplasmic reticulum (ER) stress in a dose-dependent manner. RNA-seq analysis showed that multiple cell death signalling pathways were activated after resveratrol treatment, while the use of ER stress activators (tunicamycin and thapsigargin) in combinatorial with resveratrol led to further inhibition of cancer cell survival. Results also showed that resveratrol altered the expression of several long non-coding RNAs (lncRNAs), including MEG3, PTTG3P, GAS5, BISPR, MALAT1 and H19. Knockdown of H19 in resveratrol-treated cells further enhanced the effects of resveratrol on apoptosis, ER stress and cell cycle S-phase arrest. Furthermore, the migratory ability of resveratrol-treated cells was dramatically decreased after H19 knockdown. In conclusion, resveratrol inhibited cancer cell survival, while knockdown of lncRNA H19 resulted in increased sensitivity to resveratrol therapy.

Indexed as

NeoplasmsResveratrolRNA, Long NoncodingApoptosisCell Line, TumorCell ProliferationEndoplasmic Reticulum StressHumansH19 long non-coding RNAResveratrolRNA, Long NoncodingapoptosiscancerER stresslncRNAresveratrol

Identifiers

PMID35166018
PMCPMC8995452
OpenAlexW4212819304

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.