Back to Search
Start Over
Activation-Induced Cytidine Deaminase Promotes Proliferation and Enhances Chemoresistance and Migration in B-cell Lymphoma
- Source :
- Anticancer Research. 41:237-247
- Publication Year :
- 2021
- Publisher :
- Anticancer Research USA Inc., 2021.
-
Abstract
- Background/aim Activation-induced cytidine deaminase (AID) is a DNA modifying enzyme which has an essential function in promoting antibody diversification. Its overexpression is strongly associated with B-cell derived malignancies including Burkitt lymphoma, where AID is required for the characteristic c-MYC/IGH translocation. This study aimed at defining AID's oncopathogenic role which is still poorly understood. Materials and methods We created over-expressing and knock-down cell culture models of AID, and used cellular assays to provide insight into its contribution to lymphomagenesis. Results We showed that AID expression is highly specific to, and abundantly expressed in B-cell-derived cancers and that ectopic overexpression of AID leads to rapid cell death. Using a knock-down model, we revealed that AID expression significantly impacts genomic stability, proliferation, migration and drug resistance. Conclusion AID is an important driver of lymphoma, impacting multiple cellular events, and is potentially a strong candidate for targeted therapy in lymphoma.
- Subjects :
- Cancer Research
Programmed cell death
Lymphoma, B-Cell
medicine.medical_treatment
Gene Expression
Antineoplastic Agents
Ectopic Gene Expression
Targeted therapy
Cell Movement
Cell Line, Tumor
Cytidine Deaminase
medicine
Activation-induced (cytidine) deaminase
Animals
Humans
B-cell lymphoma
Cell Proliferation
biology
Cell growth
General Medicine
Cytidine deaminase
medicine.disease
Burkitt Lymphoma
Lymphoma
Enzyme Activation
Oncology
Doxorubicin
Drug Resistance, Neoplasm
Gene Knockdown Techniques
biology.protein
Cancer research
Ectopic expression
DNA Damage
Subjects
Details
- ISSN :
- 17917530 and 02507005
- Volume :
- 41
- Database :
- OpenAIRE
- Journal :
- Anticancer Research
- Accession number :
- edsair.doi.dedup.....d942106388433b2d89353e8a93ce9c34
- Full Text :
- https://doi.org/10.21873/anticanres.14770