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

Camila A Orellana1,2, Verónica S Martínez3, Michael A MacDonald3

  • 1Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, Australia.

Insights

Chinese hamster ovary (CHO) cells are crucial for biopharmaceutical production but suffer from apoptosis, limiting protein yield. Omics studies reveal genetic targets to engineer CHO cells, reduce apoptosis, and boost productivity.

Area of Science:

  • Biotechnology
  • Cell Biology
  • Genomics

Background:

  • Chinese hamster ovary (CHO) cells are essential for biopharmaceutical manufacturing.
  • Apoptosis (programmed cell death) in CHO cells limits recombinant protein production yields.
  • Genetic engineering offers strategies to improve CHO cell performance, but further enhancements are needed.

Purpose of the Study:

  • To review omics studies in CHO cells focusing on apoptosis-related gene expression.
  • To identify potential gene targets for engineering CHO cells to reduce apoptosis.
  • To enhance CHO cell line performance and increase biopharmaceutical productivity.

Main Methods:

  • Comprehensive literature review of CHO omics studies.
  • Analysis of gene expression changes related to apoptosis.
  • Identification of gene targets for genetic engineering.

Main Results:

  • Omics analyses have identified numerous apoptosis-related genes in CHO cells.
  • Several gene targets have been validated for reducing apoptosis or enhancing proliferation.
  • Review highlights potential targets for future CHO cell line engineering.

Conclusions:

  • Omics data provide valuable insights into CHO cell apoptosis.
  • Targeted genetic engineering based on omics findings can improve CHO cell productivity.
  • Further research into identified gene targets can optimize biopharmaceutical production.

Related Concept Videos

Apoptosis01:30

Apoptosis

Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size...
13.3K
The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
7.8K
The Extrinsic Apoptotic Pathway01:17

The Extrinsic Apoptotic Pathway

The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
7.6K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
8.5K
Adaptive Mechanisms in Cancer Cells02:53

Adaptive Mechanisms in Cancer Cells

Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
6.7K
Cancer-Critical Genes II: Tumor Suppressor Genes01:05

Cancer-Critical Genes II: Tumor Suppressor Genes

Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
9.2K