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

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

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    107 Scopus citations


    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.

    Original languageEnglish (US)
    Pages (from-to)6525-6532
    Number of pages8
    Issue number43
    StatePublished - Sep 29 2005


    • Chromosome 11
    • Microcell hybrid
    • Nasopharyngeal carcinoma
    • Oligo-microarray
    • THY1

    ASJC Scopus subject areas

    • Molecular Biology
    • Genetics
    • Cancer Research


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