Dilara AKÇORA YILDIZ, Yakuphan BAYKAN, Fadime AŞIK

Proteozom inhibitörü Carfilzomib’in multipl miyelom hücrelerinde piroptozis hücre ölüm yolağı üzerine olan etkisi

Amaç: Multipl miyelom (MM), monoklonal antikor salgılayan anormal plazma hücrelerinin kemik iliğinde aşırı birikimi ile karakterize bir B hücre malignitesidir. Klinik uygulamalarda ikinci nesil proteozom inhibitörü carfilzomib (CFZ), relaps veya tedaviye dirençli hastaların tedavi rejimlerinde kullanılmaktadır. Ancak, MM hücrelerinde CFZ’in tetiklediği hücre ölümü mekanizmaları tam olarak aydınlatılamamıştır. Bu çalışmanın amacı, MM hücrelerinde CFZ’in apoptotik olmayan düzenli hücre ölüm yolaklarından biri olan piroptozis üzerine olan etkisinin araştırılmasıdır. Yöntem: İnsan RPMI 8226, U266 ve NCI H929 MM hücre hatları, CFZ’in IC50 dozları ile 48 saat süre boyunca muamele edildi. Muamele edilen hücrelerde piroptozisin önemli substratları olan GSDMD ve GSDME ile Bax ve Bcl-2 genlerinin mRNA düzeylerindeki farklılıklar kantitatif eş zamanlı PCR (qPCR) yöntemiyle belirlendi. Bulgular: NCI H929 ve RPMI 8226 hücrelerinde CFZ uygulamasının hem GSDMD hem de GSDME mRNA düzeylerinde anlamlı artışa neden olduğu belirlenirken, U266 hücrelerinde ise sadece GSDME mRNA seviyesinde anlamlı bir artış tespit edildi (p

Anahtar Kelimeler:

Multipl Miyelom, Proteazom İnhibitörü, Carfilzomib, Piroptozis, Gasdermin E

The effect of proteasome inhibitor Carfilzomib on pyroptosis cell death pathway in multiple myeloma cells

Objective: Multiple myeloma (MM), characterized by excessive accumulation of monoclonal antibody-secreting abnormal plasma cells in the bone marrow, is a B-cell malignancy. In clinical practice, the second-generation proteasome inhibitor Carfilzomib (CFZ) is used in the treatment regimens of relapsed or treatment-resistant patients. However, the mechanisms of CFZ-induced cell death in MM cells have not been fully elucidated. The aim of this study is to investigate the effect of CFZ on pyroptosis, which is one of the regulated non-apoptotic cell death pathways in MM cells. Methods: Human NCI H929, RPMI 8226, and U266 MM cell lines were treated with IC50 doses of CFZ for 48 hours. In treated cells, the differences in mRNA levels of GSDMD and GSDME, which are important substrates of pyroptosis, and in mRNA levels of Bax as well as in mRNA levels of Bcl-2 were determined by quantitative real-time PCR (qPCR) method. Results: CFZ treatment led to a significant increase in GSDMD and GSDME mRNA levels in NCI H929 and RPMI 8226 cells, while a remarkable increase was detected only in GSDME mRNA levels in U266 cells (p

Keywords:

Multiple Myeloma, Proteasome Inhibitors, Carfilzomib, Pyroptosis, Gasdermin E,

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