First Department of Internal Medicine, Hematology Unit, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
First Department of Internal Medicine, Hematology Unit, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Clin Lymphoma Myeloma Leuk. 2014 Feb;14(1):56-60. doi: 10.1016/j.clml.2013.09.002. Epub 2013 Oct 1.
Epstein-Barr virus (EBV) is a ubiquitous pathogen that chronically infects B lymphocytes and is implicated in the pathogenesis of lymphoproliferative diseases. Latent membrane protein 1 (LMP1), the major oncoprotein of the virus, has been shown to inhibit apoptosis and trigger survivin expression in malignant cell lines. LMP1 expression has been detected in patients with chronic lymphocytic leukemia, but its properties have not been studied in patients with low-grade B-cell lymphomas. Recent data show that LMP1 can simultaneously induce and inhibit apoptosis in B cells. We detected LMP1 messenger RNA (mRNA) in patients with leukemic low-grade B-cell lymphoma and correlated the expression of the antiapoptotic molecule survivin to that of LMP1 in this group of patients.
Peripheral whole blood from 64 patients with low-grade B-cell lymphoma was tested by quantitative reverse transcriptase-polymerase chain reaction (PCR) for the presence of the BXLF-1 gene of EBV, and positive samples were tested by conventional PCR for LMP1 expression. Accordingly, survivin mRNA levels were measured by quantitative reverse transcriptase PCR in all samples and compared between LMP1-positive (LMP1(+)) and LMP1(-) patients.
The BXLF-1 gene was detected in 27 of 64 patients (42%). LMP1 was expressed in 22 of 27 (81%) EBV(+) patients. Survivin expression was found to be 6.36 times higher in LMP1(-) patients than in LMP1(+) patients (P = .008).
Our results imply that in patients with non-EBV-related leukemic low-grade B-cell lymphoma, LMP1 expression is possibly correlated to apoptosis, as indicated by the lower survivin mRNA levels in LMP1(+) patients.
Epstein-Barr 病毒(EBV)是一种普遍存在的病原体,它会慢性感染 B 淋巴细胞,并与淋巴增殖性疾病的发病机制有关。潜伏膜蛋白 1(LMP1)是病毒的主要癌蛋白,已被证明可抑制凋亡并触发恶性细胞系中存活素的表达。LMP1 的表达已在慢性淋巴细胞白血病患者中检测到,但在低级别 B 细胞淋巴瘤患者中尚未对其特性进行研究。最近的数据表明,LMP1 可同时诱导和抑制 B 细胞凋亡。我们检测了白血病低级别 B 细胞淋巴瘤患者中 LMP1 的信使 RNA(mRNA),并将抗凋亡分子存活素的表达与该组患者的 LMP1 表达相关联。
通过定量逆转录-聚合酶链反应(PCR)检测 64 例低级别 B 细胞淋巴瘤患者外周全血中 EBV 的 BXLF-1 基因的存在,对阳性样本进行常规 PCR 检测 LMP1 的表达。相应地,通过定量逆转录 PCR 在所有样本中测量存活素 mRNA 水平,并在 LMP1 阳性(LMP1(+))和 LMP1 阴性(LMP1(-))患者之间进行比较。
在 64 例患者中,有 27 例(42%)检测到 BXLF-1 基因。在 27 例 EBV(+)患者中有 22 例(81%)表达 LMP1。与 LMP1(+)患者相比,LMP1(-)患者的存活素表达高 6.36 倍(P =.008)。
我们的结果表明,在非 EBV 相关的白血病低级别 B 细胞淋巴瘤患者中,LMP1 的表达可能与凋亡有关,LMP1(+)患者中存活素 mRNA 水平较低表明了这一点。