Inagaki H, Banno S, Wakita A, Ueda R, Eimoto T
Department of Pathology, Nagoya City University Medical School, Nagoya, Japan.
Mod Pathol. 1999 May;12(5):546-52.
Diffuse large B-cell lymphoma in the Revised European-American Lymphoma Classification encompasses various morphologic subtypes of diffuse large-cell lymphomas of B-cell origin. The category is biologically and clinically heterogeneous, even though it constitutes approximately 30% of all non-Hodgkin's lymphomas. Clinically, the International Prognostic Index that identifies high-risk group in aggressive non-Hodgkin's lymphomas is widely accepted. Lacking, however, are biologic or molecular prognostic markers that might aid in understanding the pathogenesis and designing specific therapies. CD44 isoforms are involved in tumor dissemination and might be associated with aggressive behavior of non-Hodgkin's lymphomas. We studied immunohistochemical expression of CD44s and CD44v6 in the tumors and examined their clinical significance in a cohort of patients with primary nodal diffuse large B-cell lymphoma who were uniformly evaluated and treated with doxorubicin-containing chemotherapy (n = 42). In contrast to CD44s signals, CD44v6 signals were weak in routinely processed non-Hodgkin's lymphoma sections. Therefore, we used a highly sensitive catalyzed reporter deposition system and successfully detected CD44v6 signals in diffuse large B-cell lymphomas. Overexpression of the isoform was verified by Southern blot of reverse transcription polymerase chain reaction products. CD44s and CD44v6 were positive in 17 (40%) of 42 and 13 (31%) of 42, respectively. CD44v6 was detected predominantly in lymphoma cells, whereas CD44s was often positive for nonneoplastic small lymphocytes as well. In univariate regression analysis, the B symptoms, being in the International Prognostic Index high-risk group, and CD44v6 expression emerged as significant parameters for poorer overall survival, but CD44s expression did not achieve statistical significance. When multivariate regression analysis was performed using the former three parameters, only CD44v6 expression remained significant (P = .017; relative risk = 3.48), indicating that CD44v6 is a molecule particularly important for predicting worse prognosis. CD44v6, which can be detected in the archival materials, might be a biologically and clinically useful marker in identifying the high-risk group in the diffuse large B-cell lymphoma category of the Revised European-American Lymphoma Classification.
在修订后的欧美淋巴瘤分类中,弥漫性大B细胞淋巴瘤涵盖了各种B细胞起源的弥漫性大细胞淋巴瘤的形态学亚型。尽管该类别约占所有非霍奇金淋巴瘤的30%,但其在生物学和临床上具有异质性。临床上,用于识别侵袭性非霍奇金淋巴瘤高危组的国际预后指数已被广泛接受。然而,目前缺乏有助于理解发病机制和设计特异性治疗的生物学或分子预后标志物。CD44异构体参与肿瘤播散,可能与非霍奇金淋巴瘤的侵袭性行为有关。我们研究了CD44s和CD44v6在肿瘤中的免疫组化表达,并在一组经统一评估且接受含阿霉素化疗的原发性淋巴结弥漫性大B细胞淋巴瘤患者(n = 42)中检验了它们的临床意义。与CD44s信号不同,在常规处理的非霍奇金淋巴瘤切片中CD44v6信号较弱。因此,我们使用了一种高灵敏度的催化报告沉积系统,并成功在弥漫性大B细胞淋巴瘤中检测到了CD44v6信号。通过逆转录聚合酶链反应产物的Southern印迹验证了该异构体的过表达。42例患者中,CD44s和CD44v6分别有17例(40%)和13例(31%)呈阳性。CD44v6主要在淋巴瘤细胞中检测到,而CD44s在非肿瘤性小淋巴细胞中也常呈阳性。在单因素回归分析中,B症状、处于国际预后指数高危组以及CD44v6表达是总生存期较差的显著参数,但CD44s表达未达到统计学意义。当使用前三个参数进行多因素回归分析时,只有CD44v6表达仍然显著(P = 0.017;相对风险 = 3.48),表明CD44v6是预测预后较差的一个特别重要的分子。在存档材料中可检测到的CD44v6,可能是修订后的欧美淋巴瘤分类中弥漫性大B细胞淋巴瘤类别里识别高危组的一个生物学和临床上有用的标志物。