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鼻咽癌的病因学因素。

Etiological factors of nasopharyngeal carcinoma.

作者信息

Tsao Sai Wah, Yip Yim Ling, Tsang Chi Man, Pang Pei Shin, Lau Victoria Ming Yi, Zhang Guitao, Lo Kwok Wai

机构信息

Department of Anatomy and Center for Cancer Research, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region.

Department of Anatomy and Center for Cancer Research, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region.

出版信息

Oral Oncol. 2014 May;50(5):330-8. doi: 10.1016/j.oraloncology.2014.02.006. Epub 2014 Mar 12.

Abstract

Nasopharyngeal carcinoma (NPC) is a common disease among southern Chinese. The major etiological factors proposed for NPC pathogenesis include genetic susceptibility, environment factors and EBV infection. In the high risk population, genetic susceptibility to NPC has been mapped to the HLA loci and adjacent genes in MHC region on chromosome 6p21. Consumption of preserved food including salted fish has been implicated in its etiology in earlier studies. Its contribution to pathogenesis of NPC remains to be determined. A decreasing trend of NPC incidence was observed in Hong Kong, Taiwan and Singapore in recent years which may be accounted by a change of dietary habits. A comprehensive epidemiological study will help to elucidate the relative importance of various risk factors in the pathogenesis of NPC. Despite the close association of EBV infection with NPC, the etiological role of EBV in NPC pathogenesis remains enigmatic. EBV infection in primary nasopharyngeal epithelial cells is uncommon and difficult to achieve. EBV does not transform primary nasopharyngeal epithelial cells into proliferative clones, which contrasts greatly with the well-documented ability of EBV to transform and immortalize primary B cells. Genetic alterations identified in premalignant nasopharyngeal epithelium may play crucial roles to support stable EBV infection. Subsequently, latent and lytic EBV gene products may drive clonal expansion and transformation of premalignant nasopharyngeal epithelial cells into cancer cells. Stromal inflammation in nasopharyngeal mucosa is believed to play an important role in modulating the growth and possibly drive the malignant transformation of EBV-infected nasopharyngeal epithelial cells. Furthermore, there are increasing evidences supporting a role of EBV infection to evade host immune surveillance. EBV-infected cells may have selective growth advantages in vivo by acquiring a stress-resistance phenotype. Understanding the etiological factors and pathogenesis of NPC will contribute effectively to the prevention and treatment of this disease.

摘要

鼻咽癌(NPC)是中国南方常见的疾病。鼻咽癌发病机制中提出的主要病因包括遗传易感性、环境因素和EB病毒感染。在高危人群中,鼻咽癌的遗传易感性已被定位到6号染色体p21区域MHC区的HLA基因座及相邻基因。早期研究表明,食用包括咸鱼在内的腌制食品与鼻咽癌病因有关。其对鼻咽癌发病机制的作用仍有待确定。近年来,香港、台湾和新加坡的鼻咽癌发病率呈下降趋势,这可能与饮食习惯的改变有关。一项全面的流行病学研究将有助于阐明各种危险因素在鼻咽癌发病机制中的相对重要性。尽管EB病毒感染与鼻咽癌密切相关,但EB病毒在鼻咽癌发病机制中的病因作用仍不明确。EB病毒在原发性鼻咽上皮细胞中的感染并不常见且难以实现。EB病毒不会将原发性鼻咽上皮细胞转化为增殖性克隆,这与EB病毒能够转化并使原发性B细胞永生化的能力形成了鲜明对比。在癌前鼻咽上皮中发现的基因改变可能在支持稳定的EB病毒感染方面发挥关键作用。随后,潜伏和裂解的EB病毒基因产物可能驱动癌前鼻咽上皮细胞的克隆扩增和转化为癌细胞。鼻咽黏膜的基质炎症被认为在调节生长以及可能驱动EB病毒感染的鼻咽上皮细胞的恶性转化中起重要作用。此外,越来越多的证据支持EB病毒感染在逃避宿主免疫监视方面的作用。EB病毒感染的细胞可能通过获得应激抗性表型在体内具有选择性生长优势。了解鼻咽癌的病因和发病机制将有效地有助于该疾病的预防和治疗。

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