Grace Zhao ISMIB Seminar

Grace Zhao - 'CfDNA epigenetics for the earlier detection of therapy-induced multi-tissue toxicity'

1:00pm - 2:00pm / Thursday 30th April 2026 / Venue: Physiology Seminar Room Nuffield Wing
Type: Seminar / Category: Department / Series: Institute of Systems, Molecular and Integrative Biology
Add this event to my calendar

Create a calendar file

Click on "Create a calendar file" and your browser will download a .ics file for this event.

Microsoft Outlook: Download the file, double-click it to open it in Outlook, then click on "Save & Close" to save it to your calendar. If that doesn't work go into Outlook, click on the File tab, then on Open & Export, then Open Calendar. Select your .ics file then click on "Save & Close".

Google Calendar: download the file, then go into your calendar. On the left where it says "Other calendars" click on the arrow icon and then click on Import calendar. Click on Browse and select the .ics file, then click on Import.

Apple Calendar: The file may open automatically with an option to save it to your calendar. If not, download the file, then you can either drag it to Calendar or import the file by going to File >Import > Import and choosing the .ics file.

Therapy-induced toxicity presents significant challenges to medicine. Current methods for toxicity detection lack sensitivity and specificity in certain cases, causing delays in diagnosis, which harm patient welfare and create financial burdens during clinical trials. A liquid biopsy assay based on cfDNA epigenetic analysis is a promising candidate for a minimally invasive approach to earlier detection of therapy-induced toxicity through the identification of highly cell-type-specific epigenetic markers. With the development and application of comprehensive cell methylation atlases, real-time monitoring of multi-tissue toxicity, leveraging next-generation sequencing, is possible. With a better understanding of cfDNA biology, a standardised diagnostic procedure based on cfDNA liquid biopsy for drug-induced toxicity, and ctDNA for efficacy, can be established. The lead time in diagnosis offered by this approach will allow for better management of treatment regimens and significantly reduce the risk of high-grade adverse events in patients, while facilitating more efficient drug development workflows. This paradigm shift to liquid biopsy-based methods paves the way for personalised treatment, heralding a new era of patient-centered clinical innovation.