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THY1是一种候选肿瘤抑制基因,在转移性鼻咽癌中表达降低。

THY1 is a candidate tumour suppressor gene with decreased expression in metastatic nasopharyngeal carcinoma.

作者信息

Lung Hong Lok, Bangarusamy Dhinoth Kumar, Xie Dan, Cheung Arthur Kwok Leung, Cheng Yue, Kumaran Mande Kuppusamy, Miller Lance, Liu Edison Tak-Bun, Guan Xin-Yuan, Sham Jonathan Shuntong, Fang Yan, Li Liqiong, Wang Nancy, Protopopov Alexey I, Zabarovsky Eugene R, Tsao Sai Wah, Stanbridge Eric J, Lung Maria Li

机构信息

Department of Biology, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong (SAR), People's Republic of China.

出版信息

Oncogene. 2005 Sep 29;24(43):6525-32. doi: 10.1038/sj.onc.1208812.

Abstract

Using oligonucleotide microarray analysis, THY1, mapping close to a previously defined 11q22-23 nasopharyngeal carcinoma (NPC) critical region was identified as showing consistent downregulated expression in the tumour segregants, as compared to their parental tumour-suppressing microcell hybrids (MCHs). Gene expression and protein analyses show that THY1 was not expressed in the NPC HONE1 recipient cells, tumour segregants, and other NPC cell lines; THY1 was exclusively expressed in the non-tumourigenic MCHs. The mechanism of THY1 gene inactivation in these cell lines was attributed to hypermethylation. Clinical study showed that in 65% of NPC specimens there was either downregulation or loss of THY1 gene expression. Using a tissue microarray and immunohistochemical staining, 44% of the NPC cases showed downregulated expression of THY1 and 9% lost THY1 expression. The frequency of THY1 downregulated expression in lymph node metastatic NPC was 63%, which was significantly higher than in the primary tumour (33%). After transfection of THY1 gene into HONE1 cells, a dramatic reduction of colony formation ability was observed. These findings suggest that THY1 is a good candidate tumour suppressor gene in NPC, which is significantly associated with lymph node metastases.

摘要

利用寡核苷酸微阵列分析,发现定位于先前定义的11q22 - 23鼻咽癌(NPC)关键区域附近的THY1,与亲代肿瘤抑制微细胞杂种(MCH)相比,在肿瘤分离株中呈现一致的表达下调。基因表达和蛋白质分析表明,THY1在NPC HONE1受体细胞、肿瘤分离株及其他NPC细胞系中均不表达;THY1仅在非致瘤性MCH中表达。这些细胞系中THY1基因失活的机制归因于高甲基化。临床研究表明,65%的NPC标本中存在THY1基因表达下调或缺失。利用组织芯片和免疫组化染色,44%的NPC病例显示THY1表达下调,9%的病例THY1表达缺失。淋巴结转移NPC中THY1表达下调的频率为63%,显著高于原发肿瘤(33%)。将THY1基因转染至HONE1细胞后,观察到集落形成能力显著降低。这些发现提示THY1是NPC中一个良好的候选肿瘤抑制基因,与淋巴结转移显著相关。

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