» Articles » PMID: 26523782

The Art of CHO Cell Engineering: A Comprehensive Retrospect and Future Perspectives

Overview
Journal Biotechnol Adv
Date 2015 Nov 3
PMID 26523782
Citations 76
Authors
Affiliations
Soon will be listed here.
Abstract

Chinese hamster ovary (CHO) cells represent the most frequently applied host cell system for industrial manufacturing of recombinant protein therapeutics. CHO cells are capable of producing high quality biologics exhibiting human-like post-translational modifications in gram quantities. However, production processes for biopharmaceuticals using mammalian cells still suffer from cellular limitations such as limited growth, low productivity and stress resistance as well as higher expenses compared to bacterial or yeast based expression systems. Besides bioprocess, media and vector optimizations, advances in host cell engineering technologies comprising introduction, knock-out or post-transcriptional silencing of engineering genes have paved the way for remarkable achievements in CHO cell line development. Furthermore, thorough analysis of cellular pathways and mechanisms important for bioprocessing steadily unravels novel target molecules which might be addressed by functional genomic tools in order to establish superior production cell factories. This review provides a comprehensive summary of the most fundamental achievements in CHO cell engineering over the past three decades. Finally, the authors discuss the potential of novel and innovative methodologies that might contribute to further enhancement of existing CHO based production platforms for biopharmaceutical manufacturing in the future.

Citing Articles

Polysorbates degrading enzymes in biotherapeutics - a current status and future perspectives.

Felix M, Waerner T, Lakatos D, Reisinger B, Fischer S, Garidel P Front Bioeng Biotechnol. 2025; 12:1490276.

PMID: 39867473 PMC: 11760601. DOI: 10.3389/fbioe.2024.1490276.


Comprehensive genome-scale CRISPR knockout screening of CHO cells.

Shin S, Kim S, Gasselin A, Lee G, Lee J Sci Data. 2025; 12(1):71.

PMID: 39814846 PMC: 11735622. DOI: 10.1038/s41597-025-04438-6.


Characterization of the Ubiquitin-Modified Proteome of Recombinant Chinese Hamster Ovary Cells in Response to Endoplasmic Reticulum Stress.

Selvaprakash K, Sideri C, Henry M, Efeoglu E, Ryan D, Meleady P Biotechnol J. 2024; 19(11):e202400413.

PMID: 39623727 PMC: 11612545. DOI: 10.1002/biot.202400413.


MiRNA Chaining for Efficient Stable Overexpression to Improve Protein Quantity and Quality in CHO Cells.

Schlossbauer P, Klingler F, Burkhart M, Leroux A, Hesse F, Otte K Methods Mol Biol. 2024; 2853:85-101.

PMID: 39460916 DOI: 10.1007/978-1-0716-4104-0_7.


Application of CRISPR/Cas9 Genome Editing to Improve Recombinant Protein Production in CHO Cells.

Grav L, Rojek J, Karottki K, Lee J, Kildegaard H Methods Mol Biol. 2024; 2853:49-69.

PMID: 39460914 DOI: 10.1007/978-1-0716-4104-0_5.