Secondary resistance to idelalisib is characterized by upregulation of IGF1R rather than by MAPK/ERK pathway mutations
Blood
.
2022 Jun 2;139(22):3340-3344.
doi: 10.1182/blood.2021014550.
Authors
Eugen Tausch
1
,
Viktor Ljungström
2
,
Andreas Agathangelidis
3
4
,
Marc Zapatka
5
,
Lydia Scarfò
3
,
Billy Michael Chelliah Jebaraj
1
,
Deyan Y Yosifov
1
5
,
Annika Müller
1
,
Veerendra Munugalavadla
6
,
Jeremiah D Degenhardt
7
,
Paolo Ghia
3
,
Richard Rosenquist
8
9
,
Stephan Stilgenbauer
1
Affiliations
1
Division of Chronic Lymphocytic Leukemia, Department of Internal Medicine III, Ulm University, Ulm, Germany.
2
Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
3
Università Vita-Salute San Raffaele and Ospedale San Raffaele, Milan, Italy.
4
Department of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.
5
German Cancer Research Center, Heidelberg, Germany.
6
Translational Medicine, Hematology Research and Development, AstraZeneca, South San Francisco, CA.
7
Research and Development, Maverick Therapeutics, Brisbane, CA.
8
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden; and.
9
Clinical Genetics, Karolinska University Laboratory, Karolinska University Hospital, Stockholm, Sweden.
PMID:
35377939
DOI:
10.1182/blood.2021014550
No abstract available
Publication types
Comment
MeSH terms
Cell Line, Tumor
Drug Resistance, Neoplasm / genetics
MAP Kinase Signaling System*
Mutation
Purines
Quinazolinones* / pharmacology
Up-Regulation
Substances
Purines
Quinazolinones
idelalisib