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BZLF1 Expression of EBV is Correlated with PARP1 Regulation on Nasopharyngeal Carcinoma Tissues

机译:EBV的BZLF1表达与PARP1对鼻咽癌组织的调控有关

摘要

Nasopharyngeal carcinomas (NPC) is a cancer that arises in the epithelial tissue that covers the inside of the nasopharyngeal mucosa and nasopharynx. Infected Epstein Barr Virus (EBV) cell in a latent infection associated with the expression of nine latent proteins. Latent Membrane Protein 1 (LMP1) is one of latent proteins, and mayor EBV oncoprotein, with functions including virus growth, and to activate BamHI-Z Leftward Reading Frame 1 (BZLF1)-EBV, which can inhibit p53 to induce apoptotic resistance, metastasis, and immune modulation. The body will respond to the expansion of EBV infection with activation of Poly(ADP-ribose)Polymerase-1 (PARP1). The objective of study is to observe the expression of BZLF1 and determine PARP1 regulation in nasopharyngeal tissues. NPC-T2, NPC-T3 and polyp tissues slides are from Ulin Hospital, Banjarmasin. To characterize the necrotic cells such as pyknosis, karyorrhexsis, and karyolysis, histological slides were stained by HE that the necrotic cells measured by using a BX-53 microscope (Olympus) with CellSens Standard software. Tissues slides were stained by using immunofluorohistochemistry with EBV-BZLF1 antibody-Mouse anti-EBV monoclonal antibody against Goat anti-mouse IgG-FITC and anti-PARP1 antibody (MC-10) against Goat anti-mouse IgG labeled Rhodamin. The expression intensities were measured by Confocal Laser Scanning Microscope (Olympus). The percentage number of necrotic cells and BZLF1 and PARP1 expression intensity were analyzed using SPSS 16.0 by one-way ANOVA test with α = 0.05, beside that we use correlate and regression analyze. The research showed that the amount of karryorhexis higher than pyknosis and karyolysis in both tissues. BZLF1 expression 1.79 INT/sel (in polyp), 2.76 INT/sel (NPC Type 2) and 4.36 INT/sel (NPC Type 3), PARP1 expression 2.25 INT/sel (in polyp), 3.31 INT/sel (NPC Type 2), dan 5.93 INT/sel (NPC Type 3).The high of intensity of expression BZLF1 induced the increasing of PARP1 expression, but not correlated with percentage of necrotic cell. Interestingly, in all tissues (NPC-T1, NPC-T2 and polyp) is increased number of karyolysis cells properly, but not in pyknosis and karryorrhexis cells. The conclusion of this study indicated that the BZLF1 induce PARP1 to repair DNA damage against EBV infection.
机译:鼻咽癌(NPC)是一种在覆盖鼻咽粘膜和鼻咽内部的上皮组织中发生的癌症。感染了爱泼斯坦巴尔病毒(EBV)细胞的潜在感染,与9种潜在蛋白的表达有关。潜在膜蛋白1(LMP1)是潜在蛋白之一,也是市长EBV癌蛋白,具有包括病毒生长在内的功能,并激活BamHI-Z向左阅读框1(BZLF1)-EBV,它可以抑制p53诱导凋亡抗性,转移和免疫调节。人体将通过激活Poly(ADP-核糖)Polymerase-1(PARP1)来响应EBV感染的扩大。研究的目的是观察鼻咽组织中BZLF1的表达并确定PARP1的调控。 NPC-T2,NPC-T3和息肉组织玻片来自Banjarmasin的Ulin医院。为了表征坏死性细胞,例如脓肿,核型渗出和溶核,通过HE染色组织切片,通过使用BX-53显微镜(Olympus)和CellSens Standard软件测量坏死细胞。通过使用免疫荧光组织化学对组织玻片进行染色,方法是使用EBV-BZLF1抗体-针对山羊抗小鼠IgG-FITC的小鼠抗EBV单克隆抗体和针对山羊抗小鼠IgG标记的Rhodamin的抗PARP1抗体(MC-10)。用共聚焦激光扫描显微镜(Olympus)测量表达强度。通过单因素方差分析(α= 0.05),使用SPSS 16.0通过SPSS 16.0分析坏死细胞的百分比,BZLF1和PARP1的表达强度。研究表明,在两个组织中,假性角质病的数量均高于萎缩和溶质。 BZLF1表达式1.79 INT / sel(在息肉中),2.76 INT / sel(NPC 2型)和4.36 INT / sel(NPC 3型),PARP1表达式2.25 INT / sel(息肉),3.31 INT / sel(NPC 2型) ),5.93 INT / sel(NPC 3型)。高表达强度BZLF1诱导PARP1表达增加,但与坏死细胞百分比无关。有趣的是,在所有组织(NPC-T1,NPC-T2和息肉)中,溶核细胞的数量均适当增加,但在乳突病和角膜下垂细胞中却没有。这项研究的结论表明BZLF1诱导PARP1修复针对EBV感染的DNA损伤。

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