Your browser does not allow JavaScript!
JavaScript is necessary for the proper functioning of this website. Please enable JavaScript or use a modern browser.
Open Science Slovenia
Open Science
DiKUL
slv
|
eng
Search
Browse
New in RUL
About RUL
In numbers
Help
Sign in
Metastatic EMT phenotype is governed by microRNA-200-mediated competing endogenous RNA networks
ID
Uhan, Sara
(
Author
),
ID
Hauptman, Nina
(
Author
)
PDF - Presentation file,
Download
(947,23 KB)
MD5: 5710BB9070C6F80149DC080B55AEDCC7
URL - Source URL, Visit
https://www.mdpi.com/2073-4409/11/1/73
Image galllery
Abstract
Epithelial–mesenchymal transition (EMT) is a fundamental physiologically relevant process that occurs during morphogenesis and organ development. In a pathological setting, the transition from epithelial toward mesenchymal cell phenotype is hijacked by cancer cells, allowing uncontrolled metastatic dissemination. The competing endogenous RNA (ceRNA) hypothesis proposes a competitive environment resembling a large-scale regulatory network of gene expression circuits where alterations in the expression of both protein-coding and non-coding genes can make relevant contributions to EMT progression in cancer. The complex regulatory diversity is exerted through an array of diverse epigenetic factors, reaching beyond the transcriptional control that was previously thought to single-handedly govern metastatic dissemination. The present review aims to unravel the competitive relationships between naturally occurring ceRNA transcripts for the shared pool of the miRNA-200 family, which play a pivotal role in EMT related to cancer dissemination. Upon acquiring more knowledge and clinical evidence on non-genetic factors affecting neoplasia, modulation of the expression levels of diverse ceRNAs may allow for the development of novel prognostic/diagnostic markers and reveal potential targets for the disruption of cancer-related EMT.
Language:
English
Keywords:
epithelial–mesenchymal transition
,
microRNA-200 family
,
epigenetic factors
,
EMT
,
ceRNA
,
lncRNA
Work type:
Article
Typology:
1.02 - Review Article
Organization:
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2022
Number of pages:
19 str.
Numbering:
Vol. 11, iss. 1, art. 73
PID:
20.500.12556/RUL-136785
UDC:
616-092
ISSN on article:
2073-4409
DOI:
10.3390/cells11010073
COBISS.SI-ID:
91683331
Publication date in RUL:
20.05.2022
Views:
857
Downloads:
110
Metadata:
Cite this work
Plain text
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Copy citation
Share:
Record is a part of a journal
Title:
Cells
Shortened title:
Cells
Publisher:
MDPI
ISSN:
2073-4409
COBISS.SI-ID:
519958809
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:
01.01.2022
Secondary language
Language:
Slovenian
Keywords:
epitelno-mezenhimski prehod
,
družina mikroRNA-200
,
epigenetski dejavniki
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
P3-0054
Name:
Patologija in molekularna genetika
Funder:
ARRS - Slovenian Research Agency
Project number:
J3-1754
Name:
Novi prognostični in diagnostični označevalci v razvoju raka debelega črevesa in danke
Funder:
ARRS - Slovenian Research Agency
Project number:
J3-3070
Name:
Določanje izvora jetrnih zasevkov iz tekočinskih biopsij
Similar documents
Similar works from RUL:
Similar works from other Slovenian collections:
Back