Autor: |
Wu Z; Department of Medical Microbiology and Immunology, Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Canada.; Department of Medicine, University of Toronto, Toronto, Canada., Nicoll M; Department of Medical Microbiology and Immunology, Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Canada.; Department of Biology, McGill University, Montreal, Canada., Ingham RJ; Department of Medical Microbiology and Immunology, Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Canada. ringham@ualberta.ca. |
Jazyk: |
angličtina |
Zdroj: |
Experimental hematology & oncology [Exp Hematol Oncol] 2021 Jan 07; Vol. 10 (1), pp. 4. Date of Electronic Publication: 2021 Jan 07. |
DOI: |
10.1186/s40164-020-00197-9 |
Abstrakt: |
Classical Hodgkin lymphoma (cHL) and anaplastic lymphoma kinase-positive, anaplastic large cell lymphoma (ALK+ ALCL) are B and T cell lymphomas respectively, which express the tumour necrosis factor receptor superfamily member, CD30. Another feature shared by cHL and ALK+ ALCL is the aberrant expression of multiple members of the activator protein-1 (AP-1) family of transcription factors which includes proteins of the Jun, Fos, ATF, and Maf subfamilies. In this review, we highlight the varied roles these proteins play in the pathobiology of these lymphomas including promoting proliferation, suppressing apoptosis, and evading the host immune response. In addition, we discuss factors contributing to the elevated expression of these transcription factors in cHL and ALK+ ALCL. Finally, we examine therapeutic strategies for these lymphomas that exploit AP-1 transcriptional targets or the signalling pathways they regulate. |
Databáze: |
MEDLINE |
Externí odkaz: |
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