AI Article Synopsis

  • - The increasing demand for recombinant therapeutic proteins is driving growth in the biopharmaceutical industry, particularly through enhanced production in mammalian cell lines like Chinese hamster ovary cells.
  • - Research has focused on improving host cell productivity using genetic manipulation techniques, including the use of MicroRNAs and various genetic engineering tools like TALEN, ZFN, and CRISPR/Cas.
  • - This study reviews methods for selecting target miRNAs in cell line engineering, evaluates gain- or loss-of-function strategies, and discusses the pros and cons of this technology based on laboratory and pilot studies.

Article Abstract

It is widely accepted that the growing demand for recombinant therapeutic proteins has led to the expansion of the biopharmaceutical industry and the development of strategies to increase recombinant protein production in mammalian cell lines such as SP2/0 HEK and particularly Chinese hamster ovary cells. For a long time now, most investigations have been focused on increasing host cell productivity using genetic manipulating of cellular processes like cell cycle, apoptosis, cell growth, protein secretory and other pathways. In recent decades MicroRNAs beside different genetic engineering tools (e.g., TALEN, ZFN, and Crisper/Cas) have attracted further attention as a tool in the genetic engineering of host cells to increase protein expression levels. Their ability to simultaneously target multiple mRNAs involved in one or more cellular processes made them a favorable tool in this field. Accordingly, this study aimed to review the methods of selecting target miRNA for cell line engineering, miRNA gain- or loss-of-function strategies, examples of laboratory and pilot studies in this field and discussed advantages and disadvantages of this technology.

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Source
http://dx.doi.org/10.1007/s10529-022-03250-1DOI Listing

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