Your browser doesn't support javascript.
RNase T2 in Inflammation and Cancer: Immunological and Biological Views.
Wu, Lei; Xu, Yanquan; Zhao, Huakan; Li, Yongsheng.
  • Wu L; Department of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, China.
  • Xu Y; Clinical Medicine Research Center, Xinqiao Hospital, Army Medical University, Chongqing, China.
  • Zhao H; Clinical Medicine Research Center, Xinqiao Hospital, Army Medical University, Chongqing, China.
  • Li Y; Department of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, China.
Front Immunol ; 11: 1554, 2020.
Article in English | MEDLINE | ID: covidwho-1194588
ABSTRACT
The RNase T2 family consists of evolutionarily conserved endonucleases that express in many different species, including animals, plants, protozoans, bacteria, and viruses. The main biological roles of these ribonucleases are cleaving or degrading RNA substrates. They preferentially cleave single-stranded RNA molecules between purine and uridine residues to generate two nucleotide fragments with 2'3'-cyclic phosphate adenosine/guanosine terminus and uridine residue, respectively. Accumulating studies have revealed that RNase T2 is critical for the pathophysiology of inflammation and cancer. In this review, we introduce the distribution, structure, and functions of RNase T2, its differential roles in inflammation and cancer, and the perspective for its research and related applications in medicine.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Disease Susceptibility / Endoribonucleases / Inflammation / Neoplasms Type of study: Prognostic study Limits: Animals / Humans Language: English Journal: Front Immunol Year: 2020 Document Type: Article Affiliation country: Fimmu.2020.01554

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Disease Susceptibility / Endoribonucleases / Inflammation / Neoplasms Type of study: Prognostic study Limits: Animals / Humans Language: English Journal: Front Immunol Year: 2020 Document Type: Article Affiliation country: Fimmu.2020.01554