Clinical Pathology Department, Ain Shams Specialized Hospital, Ain Shams University, Cairo, Egypt.
Clinical Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
PLoS One. 2023 Jul 12;18(7):e0288357. doi: 10.1371/journal.pone.0288357. eCollection 2023.
Prognostic factors in plasma cell myeloma were proved to be related to signaling pathways and associated transcription factors. RGS1 and mTOR were known to play an important role in the pathogenesis of multiple myeloma. The aim of the study was to evaluate the expression and the prognostic value of RGS1 and mTOR and their relation to clinical as well as other diagnostic criteria in multiple myeloma.
The present study included 44 denovo Myeloma patients, recruited from the Medical Oncology Department, National Cancer Institute, Cairo University. Detection of RGS1 and mTOR expression was performed using Immunohistochemical staining on bone marrow biopsy sections.
The median age was 51 years with male to female ratio 1.58:1. There was a positive highly statistically significant correlation between RGS1 and mTOR among all studied cases (p value <0.001). Regarding their prognostic value, there was a highly statistically significant association of the expression levels of RGS1 and mTOR with treatment response (p <0.001). Finally, there was a significant influence of RGS1 and mTOR on overall survival probability (p value <0.001 and <0.002 respectively) with better survival for those having low expression.
RGS1 and mTOR were suggested as poor prognostic markers in MM patients, being associated with lower response rate and inferior OS. We recommend considering RGS1 and mTOR as one of the prognostic criteria in different risk stratification and staging classifications. Further trials for RGS1 and mTOR targeting in multiple myeloma are recommended.
浆细胞骨髓瘤的预后因素已被证明与信号通路和相关转录因子有关。RGS1 和 mTOR 已知在多发性骨髓瘤的发病机制中起重要作用。本研究旨在评估 RGS1 和 mTOR 的表达及其与多发性骨髓瘤的临床和其他诊断标准的相关性及其预后价值。
本研究包括 44 例初诊骨髓瘤患者,均来自开罗大学国家癌症研究所医学肿瘤学系。使用免疫组织化学染色检测骨髓活检切片中 RGS1 和 mTOR 的表达。
中位年龄为 51 岁,男女比例为 1.58:1。在所有研究病例中,RGS1 和 mTOR 之间存在高度统计学意义的正相关(p 值<0.001)。关于它们的预后价值,RGS1 和 mTOR 的表达水平与治疗反应之间存在高度统计学意义的关联(p<0.001)。最后,RGS1 和 mTOR 对总生存概率有显著影响(p 值分别为<0.001 和<0.002),低表达者的生存情况更好。
RGS1 和 mTOR 被认为是 MM 患者的不良预后标志物,与较低的反应率和较差的 OS 相关。我们建议将 RGS1 和 mTOR 视为不同风险分层和分期分类中的预后标准之一。建议进一步开展针对 RGS1 和 mTOR 的多发性骨髓瘤靶向治疗试验。