Regulatory roles of long noncoding RNAs implicated in cancer hallmarks

Cancer cells acquire numerous biological properties (designated “cancer hallmarks”), such as cell survival and energy metabolism, that facilitate tumor growth and metastatic dissemination during development. To date, eight hallmarks of cancer have been identified that provide a logical framework for...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:International journal of cancer Ročník 146; číslo 4; s. 906 - 916
Hlavní autori: Wang, Jun, Zhang, Xuan, Chen, Wen, Hu, Xiang, Li, Jing, Liu, Changning
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Hoboken, USA John Wiley & Sons, Inc 15.02.2020
Wiley Subscription Services, Inc
Predmet:
ISSN:0020-7136, 1097-0215, 1097-0215
On-line prístup:Získať plný text
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Popis
Shrnutí:Cancer cells acquire numerous biological properties (designated “cancer hallmarks”), such as cell survival and energy metabolism, that facilitate tumor growth and metastatic dissemination during development. To date, eight hallmarks of cancer have been identified that provide a logical framework for understanding the remarkable diversity of neoplastic diseases, as proposed by Douglas Hanahan and Robert A. Weinberg. Long noncoding RNAs (lncRNAs), a category of transcripts widely demonstrated to exert significant regulatory effects on biological processes, have attracted considerable research attention due to their association with the occurrence and development of cancer. The mechanisms by which lncRNAs exert their functions require elucidation to optimize their potential utility as alternative biomarkers and therapeutic targets during tumor occurrence and progression. In this review, we have discussed recent research progress on lncRNAs involved in various cancer hallmarks and their related mechanisms of action, with a view to providing an updated picture of their immense therapeutic potential in the fight against cancer.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
ISSN:0020-7136
1097-0215
1097-0215
DOI:10.1002/ijc.32277