Down-regulation of ING4 is associated with initiation and progression of lung cancer

被引:79
作者
Jara-Lazaro, Ana Richelia [1 ]
Akhilesh, Meenakshi [1 ]
Thike, Aye Aye [1 ]
Lui, Philip Chi-Wai [2 ]
Tse, Gary Man-Kit [2 ]
Tan, Puay Hoon [1 ]
机构
[1] Singapore Gen Hosp, Dept Pathol, Singapore 169608, Singapore
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Anat & Cellular Pathol, Hong Kong, Hong Kong, Peoples R China
关键词
ING4; expression; lung cancer; mRNA; tumour suppressor gene; MAMMARY PHYLLODES TUMORS; CORE NEEDLE-BIOPSY; PREOPERATIVE DIAGNOSIS; BREAST; FIBROADENOMA; EXPRESSION; FEATURES; LESIONS;
D O I
10.1111/j.1365-2559.2010.03607.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: Tumour suppressor ING4 is one of ING family genes, which are involved in cell cycle arrest, gene transcription regulation, DNA repair and apoptosis. ING4 inhibition has been reported in various tumours, including gliomas, breast tumours, and stomach adenocarcinoma. The aim was to evaluate ING4 expression in lung cancers. Method and results: By immunohistochemistry of 246 lung tumour tissues, reduced ING4 nuclear and cytoplasmic expression were both revealed in lung cancer and associated with tumour grade. Interestingly, compared with normal tissues, we found more tumours with ING4 expression in the cytoplasm higher than in the nucleus. Nuclear ING4 inhibition correlated with the tumour stage and lymph node metastasis. Consistent with these findings, semiquantitative reverse transcriptase-polymerase chain reaction and Western blotting demonstrated decreased ING4 mRNA and expression in 100% (50/50) tumour tissues. Furthermore, ING4 expression was lower in grade III than in grades I-II tumours. Reduced ING4 mRNA correlated with lymph node metastasis. Conclusions: Our results indicate that overall inhibition of ING4 expression and ING4 expression higher in cytoplasm than in nucleus of tumour cells may be involved in the initiation and progression of lung cancers, and thus, analysis for ING4 expression may be useful as a clinical diagnostic and prognostic tool for lung cancer.
引用
收藏
页码:220 / 232
页数:13
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