Etkind Polly R, Stewart Alexandre F R, Dorai Thambi, Purcell Daniel J, Wiernik Peter H
Our Lady of Mercy Medical Center-Comprehensive Cancer Center, New York Medical College, Bronx, New York, USA.
Clin Cancer Res. 2004 Sep 1;10(17):5656-64. doi: 10.1158/1078-0432.CCR-03-0364.
In a previous study, we had detected the presence of mouse mammary tumor virus (MMTV)-like envelope (ENV) gene sequences in both the breast tumors and non-Hodgkin's lymphoma tissue of two of our breast tumor patients who had been diagnosed simultaneously with both malignancies. The aim of this study was to determine if MMTV-like DNA sequences are present in the breast tumors and non-Hodgkin's lymphomas of additional patients suffering from both malignancies and if so to characterize these sequences in detail.
DNA was extracted from formalin-fixed, paraffin-embedded tissue sample blocks of breast tumors and non-Hodgkin's lymphomas from patients suffering from both malignancies. A 250-bp region of the MMTV ENV gene and a 630-bp region of the MMTV long terminal repeat (LTR) open reading frame (ORF) that encodes the MMTV superantigen (sag) gene were amplified by PCR from the isolated DNA. Amplified products were analyzed by Southern blotting, cloned, and sequenced.
MMTV-like ENV and LTR sequences were detected in both the breast tumors and non-Hodgkin's lymphomas of 6 of 12 patients suffering from both malignancies. A novel mutant of the MMTV ENV gene was identified in these patients. Characterization of the MMTV-like LTR highly variable sag sequences revealed total or nearly total identity to three distinct MMTV proviruses from two different branches of the MMTV phylogenetic tree.
The presence of MMTV-like ENV and LTR sequences in both the breast tumors and non-Hodgkin's lymphomas of 6 additional patients suggests a possible involvement of these sequences in these two malignancies. MMTV-like LTR sequence homology to different MMTV proviruses revealed the presence of more than one strain of MMTV-like sequences in each individual suggesting the possibility of multiple infections in these patients.
在之前的一项研究中,我们在两名同时被诊断患有乳腺癌和非霍奇金淋巴瘤的乳腺癌患者的乳腺肿瘤组织和非霍奇金淋巴瘤组织中,检测到了小鼠乳腺肿瘤病毒(MMTV)样包膜(ENV)基因序列。本研究的目的是确定在其他同时患有这两种恶性肿瘤的患者的乳腺肿瘤和非霍奇金淋巴瘤中是否存在MMTV样DNA序列,如果存在,则对这些序列进行详细表征。
从同时患有这两种恶性肿瘤的患者的福尔马林固定、石蜡包埋的乳腺肿瘤和非霍奇金淋巴瘤组织样本块中提取DNA。通过聚合酶链反应(PCR)从分离出的DNA中扩增MMTV ENV基因的一个250bp区域和MMTV长末端重复序列(LTR)开放阅读框(ORF)的一个630bp区域,该开放阅读框编码MMTV超抗原(sag)基因。对扩增产物进行Southern印迹分析、克隆和测序。
在12名同时患有这两种恶性肿瘤的患者中,有6名患者的乳腺肿瘤和非霍奇金淋巴瘤中检测到了MMTV样ENV和LTR序列。在这些患者中鉴定出了一种新的MMTV ENV基因突变体。对MMTV样LTR高度可变的sag序列的表征显示,与MMTV系统发育树两个不同分支的三种不同MMTV前病毒具有完全或几乎完全的同一性。
另外6名患者的乳腺肿瘤和非霍奇金淋巴瘤中存在MMTV样ENV和LTR序列,这表明这些序列可能与这两种恶性肿瘤有关。MMTV样LTR序列与不同MMTV前病毒的同源性表明,每个个体中存在不止一种MMTV样序列,提示这些患者可能存在多重感染。