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Program

Wednesday, September 25, 2024

RNA systems biology

09:35 – 09:55

Manuel Irimia, Centre for Genomic Regulation, Barcelona, Spain

10:00 – 10:20

Katharina Höfer, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany

10:50 – 11:10

Mary A. O’Connell, Central European Institute of Technology (CEITEC), Brno, Czech Republic

11:15 – 11:35

Martin Akerman, Envisagenics Inc. New York, USA

Poster Teasers

11:40 – 12:00

The Interplay of Transcription and Splicing

13:00 – 13:20

Maria Carmo-Fonseca, Institute for Molecular Medicine (IMM), University of Lisbon, Portugal

miRNA-Based Logic Circuits Encoded on Self-Amplifying RNA for Highly Specific Cancer Cell Classification

13:25 - 13:45

Ron Weiss, Massachusetts Institute of Technology, USA

Development of FTO inhibitors for mRNA stabilization to treat AML cancer

13:50 - 14:10

Amir MorRNAble, Ness Ziona, Israel

RNA therapeutics development

14:15-14:20

Opening Remarks:  Rotem Karni, The Institute for Medical Research Israel-CanadaHebrew University- Hadassah Medical School, Israel

Keynote Lecture | Antisense Therapy for Diffuse Midline Glioma

14:20 - 15:00

Adrian R. Krainer, Cold Spring Harbor Laboratory, New York, USA

REM-422, a small molecule that reprograms RNA processing to target MYB-driven hematological and solid cancers

16:00 - 16:20

Silvia Buonamici, Remix Therapeutics, Watertown, MA, USA

Oral splicing-regulation therapy for genetic diseases and cancer

16:25 - 16:45

Masatoshi Hagiwara, MD & PhD, Professor & Chairman, Graduate School of Medicine, Department of Drug Discovery Medicine, Kyoto University, Japan

Neutrophil-specific mRNA delivery - shooting at a moving target​

16:50 - 17:10

Zvika Granot, Faculty of Medicine, Hebrew University, Jerusalem, Israel

Panel Discussion: Transforming Science into Practical Solutions: Insights from the CanceRNA Consortium

17:15 - 18:45

Tamar Raz, CEO, Hadasit Medical Research Services and Development, Jerusalem, Israel

This panel will delve into the critical business and commercialization strategies necessary to translate the CancerRNA Consortium’s research findings into tangible medical solutions and products. We will explore the primary barriers and challenges associated with commercializing RNA-based therapeutics, with a focus on innovations in cancer treatment. Additionally, the discussion will highlight how partners within the CancerRNA Consortium are addressing these challenges to advance effective new anti-cancer therapies.

Thursday, September 26, 2024

RNA therapeutics development (cont.)

Splice-switching Antisense Oligonucleotide Drug Discovery for Rare Neurodegenerative Diseases

08:50 - 09:10

Michelle L. Hastings, University of Michigan, Ann Arbor, MI, USA

Modulating mRNA stability for genetic diseases and cancer therapy

09:15 - 09:35

Rotem Karni, The Institute for Medical Research Israel-Canada, Hebrew University- Hadassah Medical School, Israel

RNA splicing in cancer

Building specificity of anti-tumor splicing inhibitors targeting SF3B1.

10:50 – 11:10

Juan Valcarcel, Centre for Genomic Regulation, Barcelona, Spain

11:15 – 11:35

Florian Heyd, Free University of Berlin, Germany

Alternative splicing of immune receptors as a regulatory mechanism

11:40 – 12:00

Michal Lotem, Hadassah Hebrew University Medical Center, Jerusalem, Israel

12:00 – 12:20

Niels Schaft, University of Erlangen, Erlangen, Germany

Poster Session

12:55 - 13:30

TBD

14:30 - 14:50

TBD

A-to-I RNA editing in cancer

15:50 – 16:10

Erez Levanon, Bar Ilan University, Ramat Gan, Israel 

Friday, September 27, 2024

CanceRNA Internal Meeting | RNA therapeutics

09:00 - 16:00
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