International Journal of Pharmacology

Volume 18 (5), 850-855, 2022


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NF-κB Signaling Pathway and Efficacy of Bortezomib-Based Combination Chemotherapy in Patients with Non-Hodgkin's Lymphoma

Jie Wang and Ting Liu

Background and Objective: The efficacy of bortezomib-based chemotherapy on Non-Hodgkin's Lymphoma (NHL) patients has been a controversial question. Therefore, in this study, we evaluated whether a different efficacy of chemotherapy in patients with a variety of NHL subtypes. Materials and Methods: We reviewed the electronic medical records of West China Hospital of Sichuan University from January, 2004-2014 and included 48 NHL patients treated with at least two cycles of bortezomib-based chemotherapy. Results: On immunostaining, 18 (35.7%) and 16 (33.3%) presented p65 and RelB nuclear staining patterns, respectively. After treatment, 4 patients (13.3%) with p65-negative were complete remission and 8 (44.4%) with p65-positive were complete remission. The complete remission rate in patients with p65-positive was higher than those with negative (p<0.0001). NF-κB-activated p65 was related to a high rate of complete remission (OR: 4.80, 95% CI: 1.173, 19.6) for bortezomib treatment, the activated Relb was related with a high risk of inefficacy (OR: 0.045, 95% CI: 0.05, 0.395) for bortezomib treatment. NF-κB and Relb activation should be monitored for helping bortezomib therapy selection. Conclusion: We found that the positive expression of p65 after nuclear staining and the negative expression of RelB after nuclear staining tended to indicate an effective treatment of bortezomib-based combination chemotherapy. However, due to the limited number of participants, further large scale, well-designed, prospective studies are warranted to confirm our findings.

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How to cite this article:

Jie Wang and Ting Liu, 2022. NF-κB Signaling Pathway and Efficacy of Bortezomib-Based Combination Chemotherapy in Patients with Non-Hodgkin's Lymphoma. International Journal of Pharmacology, 18: 850-855.


DOI: 10.3923/ijp.2022.850.855
URL: https://ansinet.com/abstract.php?doi=ijp.2022.850.855

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