Up-regulated biglycan expression correlates with the malignancy in human colorectal cancers

被引:73
作者
Gu, Xiaohu [2 ]
Ma, Yegang [2 ]
Xiao, Jingdong [3 ]
Zheng, Hongxin [4 ]
Song, Chun [2 ]
Gong, Yuehua [5 ]
Xing, Xiaojing [1 ]
机构
[1] Liaoning Canc Hosp & Inst, Dept Internal Oncol, Shenyang 110042, Peoples R China
[2] Liaoning Canc Hosp & Inst, Dept Surg Oncol, Shenyang 110042, Peoples R China
[3] Liaoning Univ Tradit Chinese Med, Dept Digest Dis, Shenyang 110032, Peoples R China
[4] Liaoning Univ Tradit Chinese Med, Dept Basic Chinese Med, Shenyang 110032, Peoples R China
[5] China Med Univ, Dept Oncol, Shenyang 110001, Peoples R China
关键词
Biglycan; Colorectal cancer; Quantitative real-time RT-PCR; Malignancy; EXTRACELLULAR-MATRIX; POTENTIAL MARKER; GASTRIC-CANCER; TUMOR-MARKERS; GENES; STATISTICS; CARCINOMA; COLON;
D O I
10.1007/s10238-011-0155-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Biglycan, an extracellular matrix protein, has been implicated in the oncogenesis and cancer development in various types of human cancer. The clinical significance of biglycan in colorectal cancer, however, remains unclear. In the present study, biglycan mRNA expression was analyzed in 110 samples (primary colorectal tumor and matched adjacent normal tissue) derived from 55 patients with colorectal cancer using quantitative real-time RT-PCR. The correlations between biglycan up-regulation and the clinicopathological data were also evaluated. We found that the up-regulation of biglycan occurred in 61.8% (34/55) of colorectal cancer tissues, and biglycan expression in colorectal cancer tissues was markedly higher than that in corresponding normal tissues (P = 0.0264). Moreover, statistical analysis displayed a significant correlation in biglycan up-regulation with poor tumor differentiation (P = 0.009), lymph node metastasis (P = 0.041), and distant metastasis (P = 0.036). However, there was no significant correlation between biglycan up-regulation and other clinicopathological factors (all P > 0.05). In conclusion, biglycan may be a potential marker for the malignancy of colorectal cancer.
引用
收藏
页码:195 / 199
页数:5
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