Gene Expression Analysis Using a Highly Sensitive DNA Microarray for Colorectal Cancer Screening

被引:0
作者
Koga, Yoshikatsu [1 ]
Yamazaki, Nobuyoshi [1 ,2 ]
Takizawa, Satoko [3 ]
Kawauchi, Junpei [3 ]
Nomura, Osamu [3 ]
Yamamoto, Seiichiro [4 ]
Saito, Norio [2 ]
Kakugawa, Yasuo [5 ]
Otake, Yosuke [5 ]
Matsumoto, Minori [5 ]
Matsumura, Yasuhiro [1 ]
机构
[1] Natl Canc Ctr Hosp East, Div Dev Therapeut, Res Ctr Innovat Oncol, Kashiwa, Chiba 2778577, Japan
[2] Natl Canc Ctr Hosp East, Colorectal & Pelv Surg Div, Kashiwa, Chiba 2778577, Japan
[3] Toray Industries Ltd, New Frontiers Res Labs, Kamakura, Kanagawa, Japan
[4] Natl Canc Ctr, Colorectal Surg Div, Tokyo, Japan
[5] Natl Canc Ctr, Screening Technol & Dev Div, Res Ctr Canc Prevent & Screening, Tokyo 104, Japan
基金
日本学术振兴会;
关键词
Cancer screening; gene profiling; colorectal cancer; fecal RNA; fecal occult blood test; DNA microarray; FECAL OCCULT-BLOOD; SIDED COLON-CANCER; STOOL DNA; POPULATION; MORTALITY; RNA; CALPROTECTIN; COLONOSCOPY; SURVIVAL; JAPAN;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Half of all patients with small, right-sided, non-metastatic colorectal cancer (CRC) have negative results for the fecal occult blood test (FORT). In the present study, the usefulness of CRC screening with a highly sensitive DNA microarray was evaluated in comparison with that by FOBT using fecal samples. Materials and Methods: A total of 53 patients with CRC and 61 healthy controls were divided into "training" and "validation sets". For the gene profiling, total RNA extracted from 0.5 g of feces was hybridized to a highly sensitive DNA chip. Results: The expressions of 43 genes were significantly higher in the patients with CRC than in healthy controls (p<0.05). In the training set, the sensitivity and specificity of the DNA chip assay using six genes were 85.4% and 85.2%, respectively. On the other hand, in the validation set, the sensitivity and specificity of the DNA chip assay were 85.2% and 85.7%, respectively. The sensitivities of the DNA chip assay were higher than those of FORT in cases of the small, right-sided, early-CRC, tumor invading up to the muscularis propria (i.e. surface tumor) subgroups. In particular, the sensitivities of the DNA chip assay in the surface tumor and early-CRC subgroups were significantly higher than those of FOBT (p=0.023 and 0.019, respectively.). Conclusion: Gene profiling assay using a highly sensitive DNA chip was more effective than FORT at detecting patients with small, right-sided, surface tumor, and early-stage CRC.
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页码:169 / 176
页数:8
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