Department of Pediatrics, Faculty of Medicine. Tanta University. Egypt.
Department of Clinical Pathology, Faculty of Medicine. Tanta University. Egypt.
Mediterr J Hematol Infect Dis. 2014 Apr 7;6(1):e2014029. doi: 10.4084/MJHID.2014.029. eCollection 2014.
Acute Lymphoblastic leukemia (ALL) is a malignant disorder of lymphoid progenitor cells that proliferate and replace the normal hematopoietic cells of the bone marrow. Protease-activated receptors (PARs) comprise a family of trans-membrane G-protein coupled receptors. Protease-activated receptor 1 (PAR-1) is a typical member of this family of receptors that mediate cellular responses to thrombin and related proteases. PAR1 is expressed by a wide range of tumor cells and can promote tumor growth, invasion and metastasis. The aim of this work was to study the role of PAR-1 expression in newly diagnosed ALL patients.
This study was conducted on 44 children with newly diagnosed ALL who were admitted to Hematology Unit, Pediatric department, Tanta University Hospital including 24 males and 20 females with their age ranged from 4-17 years and their mean age value of 9.06±3.26. All patients were subjected to complete history taking, thorough clinical examination, bone marrow aspiration and flow cytometric analysis for detection of PAR-1 expression by malignant cells.
PAR-1 was positive in 18 cases (41%) and negative in 26 cases (59%) of studied patients. This study showed no significant relation between PAR-1 expression and age, sex and most of the clinical data including hepatomegaly, splenomegaly and purpura while generalized lymphadenopathy was significantly higher in PAR-1 positive group. PAR-1 positive expression was associated with some bad prognostic laboratory parameters including higher hemoglobin, higher white blood cells, higher peripheral blood and bone marrow blast cells, higher serum LDH and lower platelets count. No significant association was detected between PAR-1 expression and immunophenotyping. There were significantly higher remission rates in PAR-1 negative group and significantly higher relapse and death rates in PAR-1 positive group.
From this study, it could be concluded that PAR-1 expression on ALL cells represents an important adverse prognostic factor.
PAR-1 expression should be routinely investigated for better prognostic assessment of ALL patients at diagnosis and should be taken in consideration in designing future therapeutic strategies based on patients- specific risk factors.
急性淋巴细胞白血病(ALL)是一种恶性淋巴祖细胞疾病,其增殖并取代骨髓中正常的造血细胞。蛋白酶激活受体(PARs)构成了跨膜 G 蛋白偶联受体家族。蛋白酶激活受体 1(PAR-1)是该受体家族的典型成员,介导细胞对凝血酶和相关蛋白酶的反应。PAR1 由广泛的肿瘤细胞表达,并能促进肿瘤生长、侵袭和转移。本工作旨在研究 PAR-1 表达在新诊断 ALL 患者中的作用。
本研究对坦塔大学医院儿科血液科收治的 44 例新诊断 ALL 患儿进行了研究,包括 24 例男性和 20 例女性,年龄 4-17 岁,平均年龄为 9.06±3.26 岁。所有患者均接受详细病史询问、全面临床检查、骨髓抽吸和流式细胞术分析,以检测恶性细胞中 PAR-1 的表达。
在研究的患者中,PAR-1 阳性 18 例(41%),阴性 26 例(59%)。本研究显示,PAR-1 表达与年龄、性别和大多数临床数据(包括肝脾肿大和紫癜)无显著关系,但全身淋巴结肿大在 PAR-1 阳性组中明显较高。PAR-1 阳性表达与一些不良预后的实验室参数相关,包括较高的血红蛋白、较高的白细胞、外周血和骨髓原始细胞较高、较高的血清 LDH 和较低的血小板计数。PAR-1 表达与免疫表型无显著相关性。PAR-1 阴性组缓解率较高,PAR-1 阳性组复发和死亡率较高。
本研究表明,ALL 细胞上的 PAR-1 表达是一个重要的不良预后因素。
PAR-1 表达应在新诊断 ALL 患者中常规检测,以更好地评估预后,并应根据患者的特定危险因素在设计未来的治疗策略时加以考虑。