De Rossi G, Tenca C, Cerruti G, Favre A, Zarcone D, Tabilio A, Mauro F R, Annino L, Grossi C E
Hematology, Human Biopathology Department, University La Sapienza, Rome, Italy.
Leuk Lymphoma. 1994 Dec;16(1-2):31-6. doi: 10.3109/10428199409114137.
Adhesion molecule expression on acute and chronic lymphoid leukemia cells of B lineage (B-ALL and B-CLL) may subserve several functions. Adhesion of leukemic cells to endothelial cells and to extracellular matrix components is relevant to homing, trafficking and spread of the malignant cells, and thus to clinical presentation, course and disease prognosis. Adhesive interactions between malignant cells and accessory cells, particularly stromal cells in the bone marrow environment, may support growth of the malignant cells via cytokine-delivered messages. They may also deliver signals that prevent or trigger programmed cell death of tumor cells. Here we review data on the adhesive phenotype of leukemic blasts from pro-B (CALLA +) ALL and of cells from B-CLL cases. We show that expression of certain adhesion molecules may help define disease subsets with distinctive clinical and prognostic features. One adhesion molecule, the lymphocyte homing receptor CD44, allows definition of two groups of B-CLL patients with significantly different survival.
B 系急性和慢性淋巴细胞白血病细胞(B-ALL 和 B-CLL)上黏附分子的表达可能具有多种功能。白血病细胞与内皮细胞以及细胞外基质成分的黏附与恶性细胞的归巢、迁移和扩散相关,进而与临床表现、病程及疾病预后相关。恶性细胞与辅助细胞(尤其是骨髓环境中的基质细胞)之间的黏附相互作用可能通过细胞因子传递的信息来支持恶性细胞的生长。它们还可能传递阻止或触发肿瘤细胞程序性细胞死亡的信号。在此,我们综述了前 B 细胞(CALLA +)ALL 白血病原始细胞以及 B-CLL 病例细胞黏附表型的数据。我们发现某些黏附分子的表达可能有助于定义具有独特临床和预后特征的疾病亚组。一种黏附分子,即淋巴细胞归巢受体 CD44,可将 B-CLL 患者分为两组,其生存率有显著差异。