Stressing the Regulatory Role of Long Non-Coding RNA in the Cellular Stress Response during Cancer Progression and Therapy

被引:5
作者
Wu, Yi-Zhen [1 ]
Su, Yong-Han [1 ]
Kuo, Ching-Ying [1 ,2 ]
机构
[1] Natl Taiwan Univ, Coll Med, Dept Clin Lab Sci & Med Biotechnol, Taipei 100229, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei 100225, Taiwan
关键词
long non-coding RNA; cellular stress; therapeutic-induced stress; stress response; therapy resistance; ENDOPLASMIC-RETICULUM STRESS; DNA-DAMAGE RESPONSE; NF-KAPPA-B; OXIDATIVE STRESS; PANCREATIC-CANCER; LNCRNA; HYPOXIA; METABOLISM; P53; GROWTH;
D O I
10.3390/biomedicines10051212
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular stress response is an important adaptive mechanism for regulating cell fate decision when cells confront with stress. During tumorigenesis, tumor progression and the course of treatment, cellular stress signaling can activate subsequent response to deal with stress. Therefore, cellular stress response has impacts on the fate of tumor cells and tumor responsiveness relative to therapeutic agents. In recent years, attention has been drawn to long non-coding RNAs (lncRNAs), a novel class of RNA molecules with more than 200 nucleotides in length, which has little protein-coding potential and possesses various functions in multiple biological processes. Accumulating evidence has shown that lncRNAs are also engaged in the regulation of cellular stress response, particularly in cancers. Here, we summarize lncRNAs that have been reported in the adaptive response to major types of cellular stress including genotoxic, hypoxic, oxidative, metabolic and endoplasmic reticulum stress, all of which are often encountered by cancer cells. Specifically, the molecular mechanisms of how lncRNAs regulate cellular stress response during tumor progression or the development of therapy resistance are emphasized. The potential clinical applications of stress-responsive lncRNAs as biomarkers will also be discussed.
引用
收藏
页数:23
相关论文
共 142 条
[1]   Non-Coding RNAs Associated With Radioresistance in Triple-Negative Breast Cancer [J].
Aranza-Martinez, Alberto ;
Sanchez-Perez, Julio ;
Brito-Elias, Luis ;
Lopez-Camarillo, Cesar ;
Cantu de Leon, David ;
Perez-Plasencia, Carlos ;
Lopez-Urrutia, Eduardo .
FRONTIERS IN ONCOLOGY, 2021, 11
[2]   P53 long noncoding RNA regulatory network in cancer development [J].
Aravindhan, Surendar ;
Younus, Laith A. ;
Hadi Lafta, Methaq ;
Markov, Alexander ;
Ivanovna Enina, Yulianna ;
A. Yushchenko, Natalya ;
Thangavelu, Lakshmi ;
Mostafavi, Seyed Mojtaba ;
V. Pokrovskii, Michail ;
Ahmadi, Majid .
CELL BIOLOGY INTERNATIONAL, 2021, 45 (08) :1583-+
[3]   Involvement of Long Non-Coding RNAs in Glucose Metabolism in Cancer [J].
Balihodzic, Amar ;
Barth, Dominik A. ;
Prinz, Felix ;
Pichler, Martin .
CANCERS, 2021, 13 (05) :1-21
[4]   Long Noncoding RNAs as Biomarkers in Cancer [J].
Bolha, Luka ;
Ravnik-Glavac, Metka ;
Glavac, Damjan .
DISEASE MARKERS, 2017, 2017
[5]   LncRNA HOTAIR acts as competing endogenous RNA to control the expression of Notch3 via sponging miR-613 in pancreatic cancer [J].
Cai, Huihua ;
Yao, Jie ;
An, Yong ;
Chen, Xuemin ;
Chen, Weibo ;
Wu, Di ;
Luo, Boyang ;
Yang, Yong ;
Jiang, Yong ;
Sun, Donglin ;
He, Xiaozhou .
ONCOTARGET, 2017, 8 (20) :32905-32917
[6]   Therapeutic targeting of cellular stress responses in cancer [J].
Chen, Miao ;
Xie, Songbo .
THORACIC CANCER, 2018, 9 (12) :1575-1582
[7]   Involvement of endoplasmic reticulum stress and p53 in lncRNA MEG3-induced human hepatoma HepG2 cell apoptosis [J].
Chen, Rui-Pei ;
Huang, Zhen-Lun ;
Liu, Li-Xuan ;
Xiang, Meng-Qi ;
Li, Guo-Ping ;
Feng, Jia-Lin ;
Liu, Bin ;
Wu, Ling-Fei .
ONCOLOGY REPORTS, 2016, 36 (03) :1649-1657
[8]   Broadening horizons: the role of ferroptosis in cancer [J].
Chen, Xin ;
Kang, Rui ;
Kroemer, Guido ;
Tang, Daolin .
NATURE REVIEWS CLINICAL ONCOLOGY, 2021, 18 (05) :280-296
[9]   LncRNA-TP53TG1 Participated in the Stress Response Under Glucose Deprivation in Glioma [J].
Chen, Xin ;
Gao, Yang ;
Li, Deheng ;
Cao, Yiqun ;
Hao, Bin .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2017, 118 (12) :4897-4904
[10]   LncRNA LOC730101 promotes osteosarcoma cell survival under energy stress [J].
Cheng, Gong ;
Li, Baoshan ;
Sun, XiuJiang ;
Cao, Zhilin ;
Zhang, GuoDong ;
Zhao, ZhongYuan ;
Zhao, Yong ;
Yu, Qian ;
Liu, WenGuang .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 496 (01) :1-6