Turbine and Daiichi Sankyo Expand ADC Discovery Collaboration
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Publications

Integrating Virtual Cell Screening and Automated Validation to Accelerate Dual Payload ADC Design 
Poster

Dana Zemel, Murat Cem Köse, Róbert Sipos, Gábor Bereczki, Richárd Izrael, Gábor Glatz, Rawan Abukhairan, Csaba Szántai-Kis, Dóra Kállai, Jerzy Woźnicki, Meera Raja, Dániel Veres, Ákos Tarcsay

The ADC field is advancing rapidly, with 17 ADCs approved to date, including 13 by the U.S. FDA, and more than 300 candidates in clinical development. Among these, dual-payload conjugates and other next-generation designs are emerging to address limitations of current ADCs. read more

Benchmarking foundation cell models for post-perturbation RNA-seq prediction 
Poster

Gerold Csendes, Gema Sanz, Kristóf Szalay, Bence Szalai

Modeling cellular phenotypes is a fundamental challenge in computational systems biology. Accurately predicting cell fate can advance our understanding of both healthy and diseased states and facilitate the identification of novel therapeutic targets. Post-perturbation transcriptomics data are particularly suited for training computational models because the causal relationship between known perturbations and the… read more

Modeling ADC payload biology using Simulated Cells – Update 
Poster

Ákos Tarcsay, István Taisz, Boldizsár Elek, Gábor Bereczki, Ágoston Mihalik, Bálint Farkas, Dániel Veres

ADCs represent a new era of targeted cancer therapy with 15 approved drugs. However, over 100 discontinued ADC programs and a similar number of active clinical trials highlight the difficulties of identifying the optimal combination of antibody, target, payload, linker, drug-antibody ratio and indication. Understanding mechanisms and factors contributing to different levels… read more

Inhibition of VCP in an in vivo model of metastatic melanoma selected based on a predictive biomarker demonstrates tumor reduction 
Poster

Aoife Campbell, Dóra Kállai, Boldizsár Elek, Csilla Hegedüs, Magdolna Djurec, Iván Fekete, Péter Szikora, Csaba Szántai-Kis, Imre Gáspár, Amrik Basran, Stephen Connolly, Dániel Veres

RAC1 and CDC42 are members of the Rho family of small GTPases that promote cell survival, cell cycle progression, proliferation, migration and invasion, therefore play a key role in anchoring independent growth, cell transformation and metastasis. Targeting RAC proteins and CDC42 holds great anti-tumoral potential. We used the Simulated Cell to perform… read more

Characterization of chromosomal instability-related dependencies through cell-specific metric for gene dosage compensation potential 
Poster

Péter Szikora, Iván Fekete, María Victoria Ruiz-Pérez, Dóra Kállai, Csilla Hegedüs, Bence Szalai, and Dániel Veres

Numerical chromosomal instability (n-CIN) is a defining characteristic of most human cancers with serious implications of large-scale alterations of the genome – such as chromosome arm level copy number changes. These kinds of somatic alterations are frequently targeting oncogenes and tumor suppressors, enriched in cancer driver events in order to shape the… read more