Genome Instability and Human Disease

Genome instability is a hallmark of cancer cells but also a cause of genetic diseases in humans. Our understanding of the causal relationships between genome instability and the development of human diseases rely on our knowledge of the basic mechanisms of DNA and RNA metabolism, from the spatial genome organization to the chromatin landscape up to the regulation of genome expression during development or in response to genotoxic stress.

The dysfunctions of these basic mechanisms related to genome metabolism underlie human diseases including cancer, aging, neurological disorders and immune deficiency.

Organization:

• Seminars by experts in the field of the mechanisms that maintain genome stability to large scale approaches (molecular signature using NGS and proteomic). Highlight how a research continuum, from basic research to clinical and translational research, provides opportunities to solve human health issues.
• Workshops: Career development, scientific communication, technological workshop, poster session, “elevator pitch”, “students will chair” session
• Poster prize
• Curie Museum visit.

The main topics are:

• Basics mechanisms for maintaining genome stability (repair, replication, DNA damage signaling, spatial genome organization).
• Dysfunction of these pathways in human diseases (cancer, aging, immunodeficiency).
• Molecular signature of genome Instability.
• The DNA damage response as anti-cancer therapeutic targets and tools for diagnostic/prognostic.