TY - JOUR
T1 - Functional and clinical significance of dysregulated microRNAs in liver cancer
AU - Huang, Po Shuan
AU - Liao, Chia Jung
AU - Huang, Ya Hui
AU - Yeh, Chau Ting
AU - Chen, Cheng Yi
AU - Tang, Hui Chi
AU - Chang, Cheng Chih
AU - Lin, Kwang Huei
N1 - Funding Information:
This research was funded by grants from Chang Gung Memorial Hospital, Chia-yi, Taiwan (CMRPG6K0031, CMRPG6K0032, CMRPG6K0033 to C.-C.C.); and from the Ministry of Science and Technology of the Republic of China (MOST 107-2314-B-182A-126-MY2-to Y.-H..H). The APC was funded by Chang Gung Memorial Hospital, Chia-yi, Taiwan.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/11/1
Y1 - 2021/11/1
N2 - Liver cancer is the leading cause of cancer-related mortality in the world. This mainly reflects the lack of early diagnosis tools and effective treatment methods. MicroRNAs (miRNAs) are a class of non-transcribed RNAs, some of which play important regulatory roles in liver cancer. Here, we discuss microRNAs with key impacts on liver cancer, such as miR-122, miR-21, miR-214, and miR-199. These microRNAs participate in various physiological regulatory pathways of liver cancer cells, and their modulation can have non-negligible effects in the treatment of liver cancer. We discuss whether these microRNAs can be used for better clinical diagnosis and/or drug devel-opment. With the advent of novel technologies, fast, inexpensive, and non-invasive RNA-based bi-omarker research has become a new mainstream approach. However, the clinical application of microRNA-based markers has been limited by the high sequence similarity among them and the potential for off-target problems. Therefore, researchers particularly value microRNAs that are specific to or have special functions in liver cancer. These include miR-122, which is specifically expressed in the liver, and miR-34, which is necessary for the replication of the hepatitis C virus in liver cancer. Clinical treatment drugs have been developed based on miR-34 and miR-122 (MRX34 and Miravirsen, respectively), but their side effects have not yet been overcome. Future research is needed to address these weaknesses and establish a feasible microRNA-based treatment strategy for liver cancer.
AB - Liver cancer is the leading cause of cancer-related mortality in the world. This mainly reflects the lack of early diagnosis tools and effective treatment methods. MicroRNAs (miRNAs) are a class of non-transcribed RNAs, some of which play important regulatory roles in liver cancer. Here, we discuss microRNAs with key impacts on liver cancer, such as miR-122, miR-21, miR-214, and miR-199. These microRNAs participate in various physiological regulatory pathways of liver cancer cells, and their modulation can have non-negligible effects in the treatment of liver cancer. We discuss whether these microRNAs can be used for better clinical diagnosis and/or drug devel-opment. With the advent of novel technologies, fast, inexpensive, and non-invasive RNA-based bi-omarker research has become a new mainstream approach. However, the clinical application of microRNA-based markers has been limited by the high sequence similarity among them and the potential for off-target problems. Therefore, researchers particularly value microRNAs that are specific to or have special functions in liver cancer. These include miR-122, which is specifically expressed in the liver, and miR-34, which is necessary for the replication of the hepatitis C virus in liver cancer. Clinical treatment drugs have been developed based on miR-34 and miR-122 (MRX34 and Miravirsen, respectively), but their side effects have not yet been overcome. Future research is needed to address these weaknesses and establish a feasible microRNA-based treatment strategy for liver cancer.
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U2 - 10.3390/cancers13215361
DO - 10.3390/cancers13215361
M3 - Review article
AN - SCOPUS:85117964138
SN - 2072-6694
VL - 13
JO - Cancers
JF - Cancers
IS - 21
M1 - 5361
ER -