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The influence of long non-coding RNAs on the response to chemotherapy in ovarian cancer
被引:15
|作者:
Wambecke, Anais
[1
,2
]
Ahmad, Mohammad
[1
,2
]
Lambert, Bernard
[1
,2
,3
]
Joly, Florence
[1
,2
]
Poulain, Laurent
[1
,2
]
Denoyelle, Christophe
[1
,2
]
Meryet-Figuiere, Matthieu
[1
,2
]
机构:
[1] Normandie Univ, UNICAEN, Interdisciplinary Res Unit Canc Prevent & Treatme, INSERM,U1086,ANTICIPE, Caen, France
[2] UNICANCER, Canc Ctr Francois Baclesse, Caen, France
[3] CNRS, Normandy Reg Delegat, Caen, France
关键词:
Long non-coding RNAs;
Ovarian cancer;
Chemotherapy;
Resistance;
PROMOTES CISPLATIN RESISTANCE;
REGULATES CELL-PROLIFERATION;
HOMOLOGOUS RECOMBINATION;
BREAST-CANCER;
EXPRESSION;
PACLITAXEL;
CARCINOMA;
NEAT1;
CHEMORESISTANCE;
OVEREXPRESSION;
D O I:
10.1016/j.ygyno.2019.12.020
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
With 240,000 new cases and 152,000 deaths per year, ovarian cancer is the leading cause of death from gynecologic malignancies. Late diagnosis because of asymptomatic development in early stages and resistance to existing treatments are the major causes of therapeutic failure in ovarian cancer. The recent discovery of tens of thousands of long non-coding RNAs and their action as oncogenes or tumor suppressors in pathways matching all the hallmarks of cancer in most-if not all-malignancies have attracted attention of the scientific community. A growing number of studies have implicated IncRNAs in diverse aspects of ovarian carcinoma biology. We present IncRNAs which have been involved in response to the different drugs currently used for the treatment of ovarian cancers, from first-line platinum salts and taxanes to the newly available PARP inhibitors. The data already available supports the potential use of several IncRNAs, alone or in combination with other molecules, as potential biomarkers for the prediction of response to treatment. Understanding the determinants of their action might reveal new potential therapeutic targets. (C) 2019 Elsevier Inc. All rights reserved.
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页码:726 / 733
页数:8
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