Gregory Hannon


Gregory James Hannon is a professor of molecular cancer biology and director of the Cancer Research UK Cambridge Institute at the University of Cambridge. He is a Fellow of Trinity College, Cambridge while also serving as a director of cancer genomics at the New York Genome Center and an adjunct professor at Cold Spring Harbor Laboratory.

Career and research

Hannon is known for his contributions to small RNA biology, cancer biology, and mammalian genomics. He has a history in discovery of oncogenes, beginning with work that led to the identification of CDK inhibitors and their links to cancer. More recently, his work has focused on small RNA biology, which led to an understanding of the biochemical mechanisms and biological functions of RNA interference. He has developed widely used tools and strategies for manipulation of gene expression in mammalian cells and animals and has generated genome-wide short hairpin RNA libraries that are available to the cancer community and was among the first to demonstrate roles for microRNAs in cancer. His laboratory also discovered the piwi-interacting RNA pathway and linked this to transposon repression and the protection of germ cell genomes. His innovations include the development of selective re-sequencing strategies, broadly termed exome capture.
In 2017, Hannon was awarded a £20 million grant to create a virtual reality interactive map of breast cancer, collaborating with researchers from Switzerland, Ireland, Canada, the USA and the UK. The project allows researchers to study how individual cells within a tumour are arranged and how they interact to allow the tumour to grow.
In 2018, it was announced Prof Hannon would guide the Functional Genomics Centre, a collaboration between Cancer Research UK and AstraZeneca. The centre, housed inside the Milner Therapeutics Institute, aims to act as a hub for genetic screens, cancer models, CRISPR tool design, and computational approaches to big data to understand genetic changes in cancer development and identify potential drug targets.

Awards and honours