Literature DB >> 32865815

'Omics driven discoveries of gene targets for apoptosis attenuation in CHO cells.

Camila A Orellana1,2, Verónica S Martínez3, Michael A MacDonald3, Matthew N Henry1, Marianne Gillard1, Peter P Gray3, Lars K Nielsen3,4,5, Stephen Mahler3, Esteban Marcellin3,4.   

Abstract

Chinese hamster ovary (CHO) cells are widely used in biopharmaceutical production. Improvements to cell lines and bioprocesses are constantly being explored. One of the major limitations of CHO cell culture is that the cells undergo apoptosis, leading to rapid cell death, which impedes reaching high recombinant protein titres. While several genetic engineering strategies have been successfully employed to reduce apoptosis, there is still room to further enhance CHO cell lines performance. 'Omics analysis is a powerful tool to better understand different phenotypes and for the identification of gene targets for engineering. Here, we present a comprehensive review of previous CHO 'omics studies that revealed changes in the expression of apoptosis-related genes. We highlight targets for genetic engineering that have reduced, or have the potential to reduce, apoptosis or to increase cell proliferation in CHO cells, with the final aim of increasing productivity.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  Chinese hamster ovary cells; apoptosis; biopharmaceutical production; genetic engineering; ‘omics

Year:  2020        PMID: 32865815     DOI: 10.1002/bit.27548

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  1 in total

1.  Engineering death resistance in CHO cells for improved perfusion culture.

Authors:  Michael A MacDonald; Matthias Nöbel; Verónica S Martínez; Kym Baker; Evan Shave; Peter P Gray; Stephen Mahler; Trent Munro; Lars K Nielsen; Esteban Marcellin
Journal:  MAbs       Date:  2022 Jan-Dec       Impact factor: 6.440

  1 in total

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