Andersson, Emma I., Bruck, Oscar, Braun, Till, Mannisto, Susanna, Saikko, Leena, Lagstrom, Sonja, Ellonen, Pekka ORCID: 0000-0001-6072-0489, Leppa, Sirpa ORCID: 0000-0002-8265-511X, Herling, Marco, Kovanen, Panu E. and Mustjoki, Satu ORCID: 0000-0002-0816-8241 (2020). STAT3 Mutation Is Associated with STAT3 Activation in CD30(+) ALK(-) ALCL. Cancers, 12 (3). BASEL: MDPI. ISSN 2072-6694

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Abstract

Peripheral T-cell lymphomas (PTCL) are a heterogeneous, and often aggressive group of non-Hodgkin lymphomas. Recent advances in the molecular and genetic characterization of PTCLs have helped to delineate differences and similarities between the various subtypes, and the JAK/STAT pathway has been found to play an important oncogenic role. Here, we aimed to characterize the JAK/STAT pathway in PTCL subtypes and investigate whether the activation of the pathway correlates with the frequency of STAT gene mutations. Patient samples from AITL (n = 30), ALCL (n = 21) and PTCL-NOS (n = 12) cases were sequenced for STAT3, STAT5B, JAK1, JAK3, and RHOA mutations using amplicon sequencing and stained immunohistochemically for pSTAT3, pMAPK, and pAKT. We discovered STAT3 mutations in 13% of AITL, 13% of ALK(+) ALCL, 38% of ALK ALCL and 17% of PTCL-NOS cases. However, no STAT5B mutations were found and JAK mutations were only present in ALK(-) ALCL (15%). Concurrent mutations were found in all subgroups except ALK(+) ALCL where STAT3 mutations were always seen alone. High pY-STAT3 expression was observed especially in AITL and ALCL samples. When studying JAK-STAT pathway mutations, pY-STAT3 expression was highest in PTCLs harboring either JAK1 or STAT3 mutations and CD30(+) phenotype representing primarily ALK ALCLs. Further investigation is needed to elucidate the molecular mechanisms of JAK-STAT pathway activation in PTCL.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Andersson, Emma I.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Bruck, OscarUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Braun, TillUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mannisto, SusannaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Saikko, LeenaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Lagstrom, SonjaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Ellonen, PekkaUNSPECIFIEDorcid.org/0000-0001-6072-0489UNSPECIFIED
Leppa, SirpaUNSPECIFIEDorcid.org/0000-0002-8265-511XUNSPECIFIED
Herling, MarcoUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kovanen, Panu E.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mustjoki, SatuUNSPECIFIEDorcid.org/0000-0002-0816-8241UNSPECIFIED
URN: urn:nbn:de:hbz:38-341995
DOI: 10.3390/cancers12030702
Journal or Publication Title: Cancers
Volume: 12
Number: 3
Date: 2020
Publisher: MDPI
Place of Publication: BASEL
ISSN: 2072-6694
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
PERIPHERAL T-CELL; LYMPHOMA; KINASE; FREQUENT; RHOA; TRANSPLANTATION; GEMCITABINE; SIGNATURES; LANDSCAPE; DIAGNOSISMultiple languages
OncologyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/34199

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