Non-coding RNAs in pancreatic ductal adenocarcinoma: New approaches for better diagnosis and therapy.
Non-coding RNAs in pancreatic ductal adenocarcinoma: New approaches for better diagnosis and therapy.
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DOI:
10.1016/j.tranon.2021.101090
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发表时间:
2021-07
影响因子:
5
通讯作者:
Uysal-Onganer P
中科院分区:
文献类型:
--
作者:
Mortoglou M;Tabin ZK;Arisan ED;Kocher HM;Uysal-Onganer P
Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies, which is usually diagnosed at an advanced stage. Non-coding RNAs (ncRNAs) have been recognized to play a central role in PDAC pathogenesis and could be used as biomarkers for PDAC. microRNAs (miRs) can act either as oncogenes or tumour suppressors in PDAC. Long non-coding RNAs (lncRNAs) are around 25% of the total RNA distribution in the human cell and their deregulation is widely implicated in PDAC carcinogenesis. Circular RNAs (circRNAs) can be potential novel biomarkers and therapeutic targets for PDAC diagnosis and treatment via their function as miR molecular "sponges", RNA-binding protein (RBP) sponges, protein translators and gene transcription regulators. Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive malignancies with a 5-year survival rate less than 8%, which has remained unchanged over the last 50 years. Early detection is particularly difficult due to the lack of disease-specific symptoms and a reliable biomarker. Multimodality treatment including chemotherapy, radiotherapy (used sparingly) and surgery has become the standard of care for patients with PDAC. Carbohydrate antigen 19–9 (CA 19–9) is the most common diagnostic biomarker; however, it is not specific enough especially for asymptomatic patients. Non-coding RNAs are often deregulated in human malignancies and shown to be involved in cancer-related mechanisms such as cell growth, differentiation, and cell death. Several micro, long non-coding and circular RNAs have been reported to date which are involved in PDAC. Aim of this review is to discuss the roles and functions of non-coding RNAs in diagnosis and treatments of PDAC.
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DOI:
10.1038/nrc.2017.99
发表时间:
2018-01
期刊:
Nature reviews. Cancer
影响因子:
--
作者:
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通讯作者:
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影响因子:
2.9
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通讯作者:
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影响因子:
37.3
作者:
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通讯作者:
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影响因子:
4
作者:
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通讯作者:
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DOI:
10.1158/1078-0432.ccr-14-0289
发表时间:
2014-11-15
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
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作者:
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通讯作者:
Blasutig IM