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The Emerging Role of RNA N6-Methyladenosine Modification in Pancreatic Cancer

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FRONTIERS IN ONCOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.927640

关键词

pancreatic cancer; non-coding RNAs; coding RNAs; RNA methylation; N6-methyladenosine (m6A)

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资金

  1. National Natural Science Foundation of China [82103295, 81801642]
  2. Natural Science Foundation of Zhejiang Province [LQ22H160062]
  3. Medical and Health Science Technology Project of Zhejiang Province [2019RC105, 2022KY516]

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This article reviews the important role of m6A modification in the development of pancreatic cancer and its molecular mechanism. It has been found that abnormal m6A modification exists in pancreatic cancer tissues and cell lines, and abnormal expressions of m6A regulators and m6A-modified genes are associated with the malignant progression of pancreatic cancer. These findings have potential applications in the clinical diagnosis, prognosis, and therapeutics of pancreatic cancer.
Pancreatic cancer (PC) is one of the most common malignant cancers, ranking the seventh highest causes of cancer-related deaths globally. Recently, RNA N6-methyladenosine (m6A) is emerging as one of the most abundant RNA modifications in eukaryote cells, involved in multiple RNA processes including RNA translocation, alternative splicing, maturation, stability, and degradation. As reported, m6A was dynamically and reversibly regulated by its writers, erasers, and readers, Increasing evidence has revealed the vital role of m6A modification in the development of multiple types of cancers including PC. Currently, aberrant m6A modification level has been found in both PC tissues and cell lines. Moreover, abnormal expressions of m6A regulators and m6A-modified genes have been reported to contribute to the malignant development of PC. Here in this review, we will focus on the function and molecular mechanism of m6A-modulated RNAs including coding RNAs as well as non-coding RNAs. Then the m6A regulators will be summarized to reveal their potential applications in the clinical diagnosis, prognosis, and therapeutics of PC.

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