
Good afternoon, and a very warm welcome to everyone joining us for today’s webinar, “Kinases, Cancer, Drugs, and Artificial Intelligence.” It is my distinct pleasure to open this session, and I want to extend a special thank you to each of you—whether you are joining from academia, the pharmaceutical industry, or clinical practice—for taking the time to be part of this important discussion.
Today, we turn our focus to a field that has become central to modern oncology: the study and therapeutic targeting of protein kinases. Over the past two decades, kinases have emerged as one of the most clinically successful classes of drug targets in cancer. These enzymes act as critical molecular switches, governing a vast network of signaling pathways that control cell proliferation, survival, and metabolism. When dysregulated—whether through mutation, overexpression, or chromosomal translocation—kinases drive the hallmark behaviors of malignancy.
It is no exaggeration to say that the discovery of kinase inhibitors has transformed the therapeutic landscape. From the groundbreaking success of imatinib in chronic myeloid leukemia to the latest generation of highly selective ATP-competitive and allosteric inhibitors, we have seen how a deep understanding of kinase biology can translate into life-saving drugs. However, we are also acutely aware of the persistent challenges: acquired resistance, off-target toxicity, and the daunting complexity of kinase signaling networks. The question is no longer simply which kinase to target, but how to target it more intelligently, more selectively, and for the right patient at the right time.
This is where artificial intelligence enters the picture, and while much of our conversation will be anchored in kinase biology, we will explore how AI is beginning to accelerate drug discovery—from structure prediction to virtual screening. Yet let us be clear: the biology remains the foundation. Our goal today is to ask how these powerful computational tools can help us navigate the complexity of the kinome and ultimately improve patient outcomes.
This is a FREE webinar. After registering, you will receive a confirmation email containing information on how to join the webinar. Registrations with academic institutional email addresses will be prioritized.
Certificates of attendance will be delivered to those who attend the live webinar.
Can’t attend? Register anyway and we’ll let you know when the recording is available to watch.
|
Speaker/Presentation |
Time in CEST |
Time in EDT |
|
Chair Introduction Dr. Jonas Cicenas |
4:00 - 4:10 pm |
10:00 - 10:10 am |
|
AI and Machine Learning in Kinase Inhibitor Development Dr. Jonas Cicenas |
4:10 - 4:30 pm |
10:10 - 10:30 am |
|
Applying Affinity Proteomics to Profile Kinome Dynamics and Inhibitor Specificity Prof. Dr. Lee M. Graves |
4:30 - 4:50 pm |
10:30 - 10:50 am |
|
Targeting Kinases in Gynecological Cancers: From Molecular Pathways to Clinical Practice Dr. Eglė Žalytė |
4:50 - 5:10 pm |
10:50 - 11:10 am |
|
Q&A |
5:10 - 5:25 pm |
11:10 - 11:25 am |
|
Closing of Webinar Dr. Jonas Cicenas |
5:25 - 5:30 pm |
11:25 - 11:30 am |

To honor Professor Tu Youyou's remarkable contributions to human health and build upon her achievements, MDPI established the Tu Youyou Award in 2016. This award aims to acknowledge exceptional scholars committed to the research fields of natural product chemistry and medicinal chemistry.
Prize:
- CHF 100,000 (to be divided equally should multiple recipients be awarded).
- An award medal and a certificate.
Nomination Deadline: 31 October 2026
For further information, please visit the Tu Youyou Award website (https://tuyouyouprize.org/).
For any inquiries, please contact the Tu Youyou Award Team at tuyouyouaward@mdpi.com.