Evidence map›Paper›PMID 35216394›Full record

ArticleInternational journal of molecular sciences2022

Interplay between ceRNA and Epigenetic Control of microRNA: Modelling Approaches with Application to the Role of Estrogen in Ovarian Cancer.

Tzy-Wei Huang, Frank H C Cheng, Ching-Cher Sanders Yan, Yu-Ming Chuang, Chien-Hong Cho, Hung-Cheng Lai, Shih-Feng Shieh, Michael W Y Chan, Je-Chiang Tsai

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Competing endogenous RNAs (ceRNAs) and drug resistance to cancer therapy.Cancer drug resistance (Alhambra, Calif.) · 2024
    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 at 6 institutions in 2 countries.

Tzy-Wei HuangDepartment of Mathematics, National Chung Cheng University, Min-Hsiung, Chia-Yi 621, Taiwan.
Frank H C ChengDepartment of Biomedical Sciences, National Chung Cheng University, Min-Hsiung, Chia-Yi 621, Taiwan.ORCID 0000-0001-5867-5754
Ching-Cher Sanders YanInstitute of Chemistry, Academia Sinica, Nangang District, Taipei 115, Taiwan.ORCID 0000-0002-9188-0036
Yu-Ming ChuangDepartment of Biomedical Sciences, National Chung Cheng University, Min-Hsiung, Chia-Yi 621, Taiwan.
Chien-Hong ChoDepartment of Applied Mathematics, National Sun Yat-Sen University, Gushan District, Kaohsiung 804, Taiwan.
Hung-Cheng LaiDepartment of Obstetrics and Gynecology, Shuang Ho Hospital, Taipei Medical University, Zhonghe District, Taipei 235, Taiwan.
Shih-Feng ShiehDepartment of Mathematics, National Taiwan Normal University, Wenshan District, Taipei 106, Taiwan.
Michael W Y ChanDepartment of Biomedical Sciences, National Chung Cheng University, Min-Hsiung, Chia-Yi 621, Taiwan.ORCID 0000-0003-1431-322X
Je-Chiang TsaiDepartment of Mathematics, National Tsing Hua University, East District, Hsinchu 300, Taiwan.
National Chung Cheng University · TWInstitute of Chemistry, Academia Sinica · TWNational Sun Yat-sen University · TWNational Taiwan Normal University · TWNational Taiwan University · TWTri-Service General Hospital · TW

Funding

Ministry of Science and Technology MOST 110-2314-B-194 -002 -MY3, 109-2115-M-007-013-MY2
6 · The paper itself

Abstract

MicroRNAs (miRNAs) play an important role in gene regulation by degradation or translational inhibition of the targeted mRNAs. It has been experimentally shown that the way miRNAs interact with their targets can be used to explain the indirect interactions among their targets, i.e., competing endogenous RNA (ceRNA). However, whether the protein translated from the targeted mRNAs can play any role in this ceRNA network has not been explored. Here we propose a deterministic model to demonstrate that in a network of one miRNA interacting with multiple-targeted mRNAs, the competition between miRNA-targeted mRNAs is not sufficient for the significant change of those targeted mRNA levels, while dramatic changes of these miRNA-targeted mRNAs require transcriptional inhibition of miRNA by its target proteins. When applied to estrogen receptor signaling pathways, the miR-193a targets E2F6 (a target of estrogen receptor), c-KIT (a marker for cancer stemness), and PBX1 (a transcriptional activator for immunosuppressive cytokine, IL-10) in ovarian cancer, such that epigenetic silencing of miR-193a by E2F6 protein is required for the significant change of c-KIT and PBX1 mRNA level for cancer stemness and immunoevasion, respectively, in ovarian cancer carcinogenesis.

Indexed as

CarcinogenesisCell Line, TumorEpigenesis, GeneticEpigenomicsEstrogensFemaleGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMicroRNAsOvarian NeoplasmsRNA, Long NoncodingRNA, MessengerSignal TransductionEstrogensMicroRNAsRNA, Long NoncodingRNA, MessengerceRNAdeterministic modelepigeneticsmicroRNAovarian cancertarget-translated protein

Identifiers

PMID35216394
PMCPMC8876507
OpenAlexW4212884320

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.