Brockelmann, Paul J., de Jong, Mathilde R. W. and Jachimowicz, Ron D. (2020). Targeting DNA Repair, Cell Cycle, and Tumor Microenvironment in B Cell Lymphoma. Cells, 9 (10). BASEL: MDPI. ISSN 2073-4409

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Abstract

The DNA double-strand break (DSB) is the most cytotoxic lesion and compromises genome stability. In an attempt to efficiently repair DSBs, cells activate ATM kinase, which orchestrates the DNA damage response (DDR) by activating cell cycle checkpoints and initiating DSB repair pathways. In physiological B cell development, however, programmed DSBs are generated as intermediates for effective immune responses and the maintenance of genomic integrity. Disturbances of these pathways are at the heart of B cell lymphomagenesis. Here, we review the role of DNA repair and cell cycle control on B cell development and lymphomagenesis. In addition, we highlight the intricate relationship between the DDR and the tumor microenvironment (TME). Lastly, we provide a clinical perspective by highlighting treatment possibilities of defective DDR signaling and the TME in mantle cell lymphoma, which serves as a blueprint for B cell lymphomas.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Brockelmann, Paul J.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
de Jong, Mathilde R. W.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Jachimowicz, Ron D.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-316385
DOI: 10.3390/cells9102287
Journal or Publication Title: Cells
Volume: 9
Number: 10
Date: 2020
Publisher: MDPI
Place of Publication: BASEL
ISSN: 2073-4409
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
CLASS-SWITCH RECOMBINATION; DEPENDENT KINASE INHIBITOR; V(D)J RECOMBINATION; CDK4/6 INHIBITOR; SYNTHETIC LETHALITY; ANTITUMOR IMMUNITY; DAMAGE RESPONSE; PARP INHIBITION; DOWN-REGULATION; WEE1 KINASEMultiple languages
Cell BiologyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/31638

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