MicroRNAs in Pancreatic Cancer and Chemoresistance

被引:1
|
作者
Pan, Yue [1 ]
Li, Kun [1 ]
Tao, Xufeng [1 ]
Li, Ning [1 ]
Huang, Jing [1 ]
Liu, Jianzhou [1 ]
Xiao, Gary Guishan [1 ,2 ,3 ,4 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, Dept Pharmaceut Sci, State Key Lab Fine Chem, Dalian, Peoples R China
[2] Univ Calif Los Angeles, Agi Hirshberg UCLA Ctr Pancreas Dis, Los Angeles, CA USA
[3] Harbor UCLA Med Ctr, Torrance, CA 90509 USA
[4] Creighton Univ, Funct Genom & Prote Labs, Med Ctr, Omaha, NE USA
基金
中国国家自然科学基金;
关键词
PDAC; drug resistance; microRNAs; metabolism; signaling pathway; DNA-DAMAGE RESPONSE; TARGETING MULTIDRUG-RESISTANCE; P-GLYCOPROTEIN; GEMCITABINE RESISTANCE; MOLECULAR-MECHANISMS; CELL-PROLIFERATION; ABC TRANSPORTERS; TUMOR-SUPPRESSOR; LUNG-CANCER; STEM-CELLS;
D O I
10.1097/MPA.0000000000001934
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Pancreatic ductal adenocarcinoma (PDAC) is one of the leading malignancies affecting human health, largely because of the development of resistance to chemotherapy/radiotherapy. There are many mechanisms that mediate the development of drug resistance, such as the transport of antineoplastic agents into cells, shifts in energy metabolism and environment, antineoplastic agent-induced DNA damage, and genetic mutations. MicroRNAs are short, noncoding RNAs that are 20 to 24 nucleotides in length and serve several biological functions. They bind to the 3 '-untranslated regions of target genes and induce target degradation or translational inhibition. MicroRNAs can regulate several target genes and mediate PDAC chemotherapy/radiotherapy resistance. The detection of novel microRNAs would not only reveal the molecular mechanisms of PDAC and resistance to chemotherapy/radiotherapy but also provide new approaches to PDAC therapy. MicroRNAs are thus potential therapeutic targets for PDAC and might be essential in uncovering new mechanisms of the disease.
引用
收藏
页码:1334 / 1342
页数:9
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