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Emerging Role of miR-345 and Its Effective Delivery as a Potential Therapeutic Candidate in Pancreatic Cancer and Other Cancers

期刊

PHARMACEUTICS
卷 13, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics13121987

关键词

PDAC; miR-345; miRNA nanodelivery

资金

  1. National Institutes of Health
  2. National Cancer Institute [R01 CA247763, R21 CA238953, P01 CA21779]
  3. Carol Vohs Johnson Chair

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miRNAs play a crucial role in cancer pathogenesis, including PDAC, and targeted treatment strategies altering miRNA levels show promising potential as therapeutic interventions. miR-345 is involved in tumor suppression in various cancers, including PDAC, and its therapeutic roles are being researched for drug development and implications. Delivery systems for miRNAs, such as miR-345, using different materials and nanoformulations are being investigated for cancer therapy.
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive malignancy with high mortality, poor prognosis, and palliative treatments, due to the rapid upregulation of alternative compensatory pathways and desmoplastic reaction. miRNAs, small non-coding RNAs, have been recently identified as key players regulating cancer pathogenesis. Dysregulated miRNAs are associated with molecular pathways involved in tumor development, metastasis, and chemoresistance in PDAC, as well as other cancers. Targeted treatment strategies that alter miRNA levels in cancers have promising potential as therapeutic interventions. miRNA-345 (miR-345) plays a critical role in tumor suppression and is differentially expressed in various cancers, including pancreatic cancer (PC). The underlying mechanism(s) and delivery strategies of miR-345 have been investigated by us previously. Here, we summarize the potential therapeutic roles of miR-345 in different cancers, with emphasis on PDAC, for miRNA drug discovery, development, status, and implications. Further, we focus on miRNA nanodelivery system(s), based on different materials and nanoformulations, specifically for the delivery of miR-345.

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