Laboratory of Hematology, CHU Lille, Lille, France.
Department of Hematology, CHU Lille, Lille, France.
Cancer Med. 2019 Mar;8(3):1279-1288. doi: 10.1002/cam4.2007. Epub 2019 Feb 10.
CD9 is a cell surface protein and belongs to the tetraspanin family. Its role in carcinomagenesis has been widely studied in solid tumors but remains controversial, depending on the cancer type. Although CD9 seems to be associated with unfavorable outcome and disease progression in acute lymphoblastic leukemia (ALL), this marker has not yet been studied in acute myeloid leukemia (AML). First, we explored its prognostic role and its association with biological factors in a cohort of 112 AML patients treated with intensive chemotherapy. CD9 was expressed in 40% of AML and was associated with a favorable outcome (event-free survival and relapse-free survival) in univariate (P = 0.009 and P = 0.048, respectively) and multivariate (P = 0.004 and P = 0.039, respectively) analyses. Interestingly, CD9 expression was different between the more immature physiologic and AML cells (CD34+CD38-) as it was also expressed in AML on putative leukemic stem cells (LSCs) but not on hematopoietic stem cells (HSCs). Hence, CD9 could be a very relevant marker for minimal residual disease (MRD) monitoring in AML based on LSC targeting.
CD9 是一种细胞表面蛋白,属于四跨膜蛋白家族。其在实体瘤中的致癌作用已得到广泛研究,但结果存在争议,取决于癌症类型。虽然 CD9 似乎与急性淋巴细胞白血病(ALL)的不良预后和疾病进展相关,但在急性髓细胞白血病(AML)中尚未对此标志物进行研究。首先,我们在接受强化化疗的 112 例 AML 患者队列中探索了其预后作用及其与生物学因素的关系。CD9 在 40%的 AML 中表达,在单因素(无事件生存和无复发生存,分别为 P=0.009 和 P=0.048)和多因素(分别为 P=0.004 和 P=0.039)分析中与良好的预后相关。有趣的是,CD9 的表达在更不成熟的生理和 AML 细胞之间存在差异(CD34+CD38-),因为它也在 AML 的假定白血病干细胞(LSCs)上表达,但不在造血干细胞(HSCs)上表达。因此,CD9 可能是基于 LSC 靶向的 AML 微小残留病(MRD)监测的一个非常相关的标志物。