L
Luisella Toschi
Researcher at Bayer HealthCare Pharmaceuticals
Publications - 9
Citations - 278
Luisella Toschi is an academic researcher from Bayer HealthCare Pharmaceuticals. The author has contributed to research in topics: Mutant & Myeloid leukemia. The author has an hindex of 5, co-authored 9 publications receiving 232 citations.
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Journal ArticleDOI
Pan-mutant IDH1 inhibitor BAY 1436032 for effective treatment of IDH1 mutant astrocytoma in vivo
Stefan Pusch,Stefan Pusch,Sonja Krausert,Viktoria Fischer,Viktoria Fischer,Jörg Balss,Jörg Balss,Martina Ott,Martina Ott,Daniel Schrimpf,Daniel Schrimpf,David Capper,David Capper,Felix Sahm,Felix Sahm,Jessica Eisel,Ann Christin Beck,Manfred Jugold,Viktoria Eichwald,Stefan Kaulfuss,Olaf Panknin,Hartmut Rehwinkel,Katja Zimmermann,Roman C. Hillig,Judith Guenther,Luisella Toschi,Roland Neuhaus,Andrea Haegebart,Holger Hess-Stumpp,Markus Bauser,Wolfgang Wick,Wolfgang Wick,Andreas Unterberg,Christel Herold-Mende,Michael Platten,Michael Platten,Andreas von Deimling,Andreas von Deimling +37 more
TL;DR: BA 1436032 has been shown to significantly prolong survival of mice intracerebrally transplanted with human astrocytoma carrying the IDH1R132H mutation and is developed a pan-inhibitor targeting tumors with different IDH 1R132 mutations.
Journal ArticleDOI
Pan-mutant-IDH1 inhibitor BAY1436032 is highly effective against human IDH1 mutant acute myeloid leukemia in vivo
Anuhar Chaturvedi,Lena Herbst,Stefan Pusch,Stefan Pusch,Lara Klett,Ramya Goparaju,Damian Stichel,Stefan Kaulfuss,Olaf Panknin,Katja Zimmermann,Luisella Toschi,Roland Neuhaus,Andrea Haegebarth,Hartmut Rehwinkel,Holger Hess-Stumpp,Markus Bauser,Tilmann Bochtler,Tilmann Bochtler,Eduard A. Struys,Amar Deep Sharma,A Bakkali,Robert Geffers,M M Araujo-Cruz,Felicitas Thol,Razif Gabdoulline,Arnold Ganser,Anthony D. Ho,A. von Deimling,A. von Deimling,Karsten Rippe,Michael Heuser,Alwin Krämer,Alwin Krämer +32 more
TL;DR: Together, BAY1436032 is highly effective against all major types of IDH1 mutant AML, including leukemic blast clearance, myeloid differentiation, depletion of leukmic stem cells and prolonged survival in two independent patient-derived xenograft IDH 1 mutant AMl mouse models.
Journal ArticleDOI
Pan-Mutant-IDH1 Inhibitor Bay-1436032 Is Highly Effective Against Human IDH1 Mutant Acute Myeloid Leukemia In Vivo
Michael Heuser,Lena Herbst,Stefan Pusch,Lara Klett,Ramya Goparaju,Damian Stichel,Stefan Kaulfuss,Olaf Panknin,Katja Zimmermann,Luisella Toschi,Roland Neuhaus,Andrea Haegebarth,Hartmut Rehwinkel,Holger Hess-Stumpp,Markus Bauser,Tilmann Bochtler,Eduard A. Struys,Amit Sharma,Abdellatif Abdellatif,Robert Geffers,Michelle Maria Araujo Cruz,Felicitas Thol,Razif Gabdoulline,Arnold Ganser,Anthony D. Ho,Andreas von Deimling,Karsten Rippe,Anuhar Chaturvedi,Alwin Kraemer +28 more
TL;DR: The novel oral pan-mutant IDH1 inhibitor BAY-1436032 is active against all IDH 1R132 mutation types and shows strong anti-leukemic activity in two independent AML PDX mouse models and clinical development is ongoing with a first in man study with Bays-14 36032 inIDH1 mutant solid tumors.
Journal ArticleDOI
Effect of oncogene activating mutations and kinase inhibitors on amino acid metabolism of human isogenic breast cancer cells.
Eung-Sam Kim,Eung-Sam Kim,Animesh Samanta,Hui Shan Cheng,Zhaobing Ding,Weiping Han,Luisella Toschi,Young-Tae Chang,Young-Tae Chang +8 more
TL;DR: The changes in amino acid metabolism induced in MCF10A, a human mammary epithelial cell line, by the sequential knock-in of K-Ras and PI3K mutant oncogenes may indicate the dependency of AA metabolism on the oncogene mutation pattern in human cancer.
Patent
2-phenyl-3-(piperazinomethyl)imidazo[1,2-a]pyridine derivatives as blockers of task-1 and task-2 channels, for the treatment of sleep-related breathing disorders
Martina Delbeck,Michael Hahn,Thomas Müller,Heinrich Meier,Klemens Lustig,Johanna Mosig,Luisella Toschi,Albus Udo,Doris Gehring,Rosenstein Bjoern +9 more
TL;DR: In this paper, a 2-phenyl-3-(piperazinomethyl)imidazo[1,2-a]pyridine derivatives were used as selective blockers of TASK-1 and TASk-3 channels, for the treatment and prevention of breathing disorders including sleep-related breathing disorders such as obstructive and central sleep apnea and snoring.