De Ramón Cristina, Rojas Elizabeta A, Misiewicz-Krzeminska Irena, Cardona-Benavides Ignacio J, Cuadrado Myriam, Isidro Isabel, Calasanz María-José, Fernandez Manuela, García-Sanz Ramón, Puig Noemi, Cedena M Teresa, Paiva Bruno, Rosiñol Laura, Martínez-López Joaquín, Bladé Joan, Lahuerta Juan J, San Miguel Jesús F, Mateos María V, Corchete Luis A, Gutiérrez Norma C
Department of Hematology, University Hospital of Salamanca Institute of Biomedical Research of Salamanca (IBSAL) Salamanca Spain.
Cancer Research Center-IBMCC (USAL-CSIC) Salamanca Spain.
Hemasphere. 2024 Dec 13;8(12):e70036. doi: 10.1002/hem3.70036. eCollection 2024 Dec.
Antiapoptotic Bcl-2 family proteins are involved in myeloma cell survival. To date, their expression in multiple myeloma (MM) patients has mostly been analyzed at the RNA level. In the present study, we quantified for the first time the protein expression of the Bcl2-family members using a capillary electrophoresis immunoassay in 120 newly diagnosed MM patients, aged ≤65 years, treated in the context of the PETHEMA/GEM2012 study. We found that the pattern of expression of Bcl-2 family proteins was highly heterogeneous among patients. Although cases with t(11;14) had significantly higher levels of Bcl-2/Bcl-xL and Bcl-2+Bim+Bax/Bcl-xL ratios than those without t(11;14), the presence of this translocation was not synonymous with such high levels of expression. Conversely, some patients with other genetic alterations also showed higher levels of those ratios. Survival analysis revealed that the high expression of Bad and Puma proteins was associated with significantly longer overall survival ( = 0.001 and < 0.001, respectively). Bcl-2 protein ratios predicting sensitivity to venetoclax were also able to distinguish patients with shorter time to progression after triplet-based induction therapy and ASCT. This is the first study to assess the expression of the most important Bcl-2 family proteins by a quantitative method in a large set of MM patients according to their cytogenetic abnormalities. We shed light on the impact of these proteins on MM prognosis, which could help to consider the levels of proteins involved in apoptosis in the development of new therapeutic strategies.
抗凋亡Bcl-2家族蛋白参与骨髓瘤细胞的存活。迄今为止,它们在多发性骨髓瘤(MM)患者中的表达大多在RNA水平进行分析。在本研究中,我们首次使用毛细管电泳免疫分析法对120例年龄≤65岁、在PETHEMA/GEM2012研究背景下接受治疗的新诊断MM患者中Bcl2家族成员的蛋白表达进行了定量。我们发现,Bcl-2家族蛋白的表达模式在患者中高度异质性。虽然t(11;14)的病例中Bcl-2/Bcl-xL以及Bcl-2+Bim+Bax/Bcl-xL比值显著高于无t(11;14)的病例,但这种易位的存在并不等同于如此高的表达水平。相反,一些有其他基因改变的患者也显示出这些比值较高。生存分析显示,Bad和Puma蛋白的高表达分别与显著更长的总生存期相关(分别为=0.001和<0.001)。预测对维奈托克敏感性的Bcl-2蛋白比值也能够区分基于三联诱导治疗和自体干细胞移植(ASCT)后进展时间较短的患者。这是第一项根据细胞遗传学异常情况,通过定量方法评估大量MM患者中最重要的Bcl-2家族蛋白表达的研究。我们阐明了这些蛋白对MM预后的影响,这有助于在制定新的治疗策略时考虑凋亡相关蛋白的水平。