The genes that help you smell could also be assisting the spread of colon cancer.
Humans have around 400 “smell-sensing” genes which activate in a combination of ways to allow us to smell the ranges of smells that we do. However, the genes have been found to be expressed in parts of the body other than the nose, with their role previously remaining a mystery. Now, a new study published in Molecular Systems Biology. has found that patients whose colon cancer cells show the “expression” of certain smell-sensing genes are more likely to have worse outcomes, especially those with more severe cases of cancer.
The expression of a gene is when the information that is stored in our DNA is translated into instructions for making proteins or other molecules. Gene expression can act as an on/off switch to control when proteins are made and how many. So, the expression of these smell-sensing genes means that the instructions for these particular genes are in use. The levels of the genes can be reduced by experimental techniques called “perturbations” to study the role of the gene in the cell.
When researching the development of cancer, a key thing to look at is the organisation of cells in body tissue. Dr Heba Sailem, Sir Henry Wellcome Research Fellow at the Institute of Biomedical Engineering and lead author on the study, along with Professor Jens Rittscher and Lucas Pelkmans (University of Zurich), explains: 'Cancer is often characterised with the loss of tissue structure which can be driven by certain gene alterations or stresses. It is crucial to understand which genes play a role in this process to be able to develop therapies that target cancer development.'
The researchers used multiple layers of Artificial Intelligence including a computer vision algorithm to detect changes in cell appearance and organisation. The algorithm was fed information from robotic microscopy, in collaboration with researchers from the University of Zurich, to image millions of colon cancer cells.
Following the perturbation (or decrease in the expression) of every gene in each individual colon cancer cell the study found that smell-sensing genes are strongly associated with how cells spread and align with each other. Reducing the expression of smell-sensing genes can inhibit cells from spreading, potentially by restraining the ability of cells to move. The same behaviour is also observed in the perturbation of key cancer genes. In contrast, having higher levels of these genes might increase cell motility.
Dr Sailem says: 'It is like activating a sixth sense that allows cancer cells to smell their way outside the toxic tumour environment which can result in spreading cancer to other parts of the body and make things worse for the patient.'
“It is like activating a sixth sense that allows cancer cells to smell their way outside the toxic tumour environment which can result in spreading cancer to other parts of the body and make things worse for the patient”
Artificial intelligence was crucial in accelerating the speed and efficiency of this research. The computer is trained using an encyclopaedia of knowledge on the functions of genes collected over decades and automates the process of identifying cell patterns in the images. Previously, this type of research would have relied on the slower and more costly method of human experts identifying examples of changes in cell appearance.
Dr Sailem says: 'Using the developed AI system, we can now learn much more from these experiments and accelerate the identification of genes that alter the structure of tissues in cancer.' Gene editing technology CRIPSR (Clustered Regularly Interspaced Short Palindromic Repeats) is now routinely used to reduce the level of every gene in the cell out of around 20,000 genes to study how changing the level of the gene affects cancer cell behaviour.
Parallel with advances in gene editing technologies, such as CRISPR, this research could enable new avenues in identifying the functions of genes in different cancer types which is vital for cancer therapy and understanding cancer evolution.