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Bio
Research
Cancer and many other human diseases arise from genetic aberrations that are either inherited or occur spontaneously in somatic cells. These defects cause abnormal activities of gene products and lead to malfunctioning of molecular and cellular interactions which may induce tumors and cause cancer progression. The central objective of our division is to understand the complexity of molecular mechanisms in the regulation of signaling networks and how these impact cancer development, metastasis, and drug resistance. To this end, we generate and maintain resources for large-scale experimentation, apply high-throughput functional genomics and proteomics technologies, and analyze candidate genes using in vitro as well as in vivo systems. Effects of perturbations (gene gain- and loss-of-function, miRNA, drugs) imposed on the signaling processes are experimentally tested and then computationally modeled. This generates mechanistic knowledge that is exploited to identify new diagnostic and prognostic markers as well as to develop novel strategies for therapeutic intervention. Our major focus here is on breast cancer, where we investigate protein and non-protein factors that are involved in the progression of different subtypes via their activities in interrelated signaling networks.
FUTURE OUTLOOK
We have already seen from our current data that signaling is not regulated in isolated pathways, but rather in complex networks. These networks involve different cell types within the tumor microenvironment which impact on the tumor cells and vice versa. We thus investigate the impact individual perturbations have, at different levels (DNA, RNA, protein, metabolite, phenotype…), on a variety of cellular pathways and in the context of different cell types. This should provide us with a better understanding of the connectivity between multi-layer interaction systems. Such information will be essential, for example, in identifying strategies that should help overcoming drug resistance and metastasis. While much of our current knowledge is based on in vitro experiments, we need to validate findings in vivo in order to prove their relevance. To this end, we generate and test animal models and challenge our hypotheses with data generated from patient samples. Our research is funded mostly by national (e.g., BMBF, Landesstiftung Baden-Württemberg, EKFS-Stiftung) and international (EU) agencies.
Cancer and many other human diseases arise from genetic aberrations that are either inherited or occur spontaneously in somatic cells. These defects cause abnormal activities of gene products and lead to malfunctioning of molecular and cellular interactions which may induce tumors and cause cancer progression. The central objective of our division is to understand the complexity of molecular mechanisms in the regulation of signaling networks and how these impact cancer development, metastasis, and drug resistance. To this end, we generate and maintain resources for large-scale experimentation, apply high-throughput functional genomics and proteomics technologies, and analyze candidate genes using in vitro as well as in vivo systems. Effects of perturbations (gene gain- and loss-of-function, miRNA, drugs) imposed on the signaling processes are experimentally tested and then computationally modeled. This generates mechanistic knowledge that is exploited to identify new diagnostic and prognostic markers as well as to develop novel strategies for therapeutic intervention. Our major focus here is on breast cancer, where we investigate protein and non-protein factors that are involved in the progression of different subtypes via their activities in interrelated signaling networks.
FUTURE OUTLOOK
We have already seen from our current data that signaling is not regulated in isolated pathways, but rather in complex networks. These networks involve different cell types within the tumor microenvironment which impact on the tumor cells and vice versa. We thus investigate the impact individual perturbations have, at different levels (DNA, RNA, protein, metabolite, phenotype…), on a variety of cellular pathways and in the context of different cell types. This should provide us with a better understanding of the connectivity between multi-layer interaction systems. Such information will be essential, for example, in identifying strategies that should help overcoming drug resistance and metastasis. While much of our current knowledge is based on in vitro experiments, we need to validate findings in vivo in order to prove their relevance. To this end, we generate and test animal models and challenge our hypotheses with data generated from patient samples. Our research is funded mostly by national (e.g., BMBF, Landesstiftung Baden-Württemberg, EKFS-Stiftung) and international (EU) agencies.
Research Interests
Papers共 350 篇Author StatisticsCo-AuthorSimilar Experts
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Diana Drago-Garcia,Suvendu Giri, Rishita Chatterjee, Arturo Simoni-Nieves, Maha Abedrabbo, Alessandro Genna, Mary Luz Uribe Rios,Moshit Lindzen,Arunachalam Sekar, Nitin Gupta, Noa Aharoni, Tithi Bhandari, Agalyan Mayalagu, Luisa Schwarzmüller,Nooraldeen Tarade, Rong Zhu, Harsha-Raj Mohan-Raju, Feride Karatekin,Francesco Roncato, Yaniv Eyal-Lubling, Tal Keidar, Yam Nof,Nishanth Belugali Nataraj, Karin Shira Bernshtein, Bettina Wagner,Nishanth Ulhas Nair, Neel Sanghvi,Ronen Alon,Rony Seger,Eli Pikarsky,Sara Donzelli,Giovanni Blandino,Stefan Wiemann,Sima Lev,Ron Prywes,Dalit Barkan,Oscar M Rueda,Carlos Caldas,Eytan Ruppin, Yosef Shiloh,Maik Dahlhoff,Yosef Yarden
Science signalingno. 883 (2025): eado3473-eado3473
Diana Drago,Suvendu Giri, Rishita Chattaerjee,Arturo Simoni Nieves, Maha Abedrabbo, Alessandro Genna, Mary Luz Uribe Rios,Moshit Lindzen,Arunachalam Sekar, Nitin Gupta, Noa Aharoni, Tithi Bhandari, Agalyan Mayalagu, Luisa Schwarzmuller,Nooraldeen Tarade, Rong Zhu,Harsha-Raj Mohan-Raju, Feride Karatekin,Francesco Roncato, Yaniv Eyal-Lubling, Tal Keidar, Yam Nof,Nishanth Belugali Nataraj, Karin Shira Bernshtein,Bettina Wagner,Nishanth Ulhas Nair, Neel Sanghvi,Ronen Alon,Rony Seger,Eli Pikarsky,Sara Donzelli,Giovanni Blandino,Stefan Wiemann,Sima Lev, Ron Prywes,Dalit Barkan,Oscar Rueda,Carlos Caldas,Eytan Ruppin, Yosef Shiloh,Maik Dahlhoff,Yosef Yarden
biorxiv(2025)
Efstathios-Iason Vlachavas,Konstantinos Voutetakis,Vivian Kosmidou,Spyridon Tsikalakis, Spyridon Roditis,Konstantinos Pateas, Ryangguk Kim,Kymberleigh Pagel,Stephan Wolf,Gregor Warsow,Antonia Dimitrakopoulou-Strauss,Georgios N. Zografos,Alexander Pintzas,Johannes Betge,Olga Papadodima,Stefan Wiemann
MOLECULAR ONCOLOGY (2025)
CANCER RESEARCHno. 7 (2024)
crossref(2024)
Alfredo Rivas-Delgado,Cristina Lopez,Guillem Clot,Ferran Nadeu,Marta Grau,Gerard Frigola,Jan Bosch-Schips,Josefine Radke,Naveed Ishaque,Miguel Alcoceba,Gustavo Tapia,Luis Luizaga,Carmen Barcena,Nicholas Kelleher,Neus Villamor,Tycho Baumann,Ana Muntanola, Juan M. Sancho-Cia,Alejandro M. Garcia-Sancho,Eva Gonzalez-Barca,Estella Matutes, Jordi A. Brito,Kennosuke Karube,Itziar Salaverria,Anna Enjuanes,Stefan Wiemann,Frank L. Heppner,Reiner Siebert,Fina Climent,Elias Campo,Eva Gine,Armando Lopez-Guillermo,Silvia Bea
HEMASPHEREno. 10 (2024)
crossref(2024)
Journal of Molecular Diagnostics (2024)
crossref(2024)
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Author Statistics
#Papers: 350
#Citation: 17641
H-Index: 68
G-Index: 126
Sociability: 8
Diversity: 4
Activity: 37
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