
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
1 NIH, Seoul, Korea and 2 Department of Biological Science, Gachon University of Medicine and Science; 3 HanCell, Inc., Incheon, Korea
Requests for reprints: Myeong Jin Nam, Department of Biological Science, Gachon University of Medicine and Science, 534-2 Yeonsu-dong Yeonsu-gu, Incheon 406-799, Korea. Phone: 82-32-820-4542; Fax: 82-32-820-4549; E-mail: genetx{at}hanmail.net
The early diagnosis of colorectal cancer and the early detection of recurrence are central to effective treatment, as prognosis is directly related to the stage of the disease. When colorectal cancer is diagnosed at an early, localized stage, 5-year survival is 90%. There is substantial interest in the identification of circulating human tumor-derived proteins in serum for the purposes of early cancer diagnosis. We have implemented an approach based on the analysis of microarray data for the identification of tumor proteins that may have utility as biomarkers in colon cancer. Expression analysis of microarray data obtained from a variety of 290 tumors and normal tissues revealed that galanin was maximally expressed in colon cancer. These findings were corroborated by real-time quantitative PCR, in which the colon cancer cell lines LOVO, HCT15, SW480, and SW620 cell showed significantly higher levels of galanin expression than did noncolon cancer cell lines. To evaluate galanin as a potential biomarker of colon cancer, a preliminary "training" set of serum from 40 healthy donors and 55 colon cancer patients was analyzed by ELISA. The data pattern was confirmed by an independent set of 90 masked serum samples: 24 from healthy donors and 66 from colon cancer patients. This result yielded a sensitivity of 69.7% [95% confidence interval (95% CI), 57.1-80.4], specificity of 75.0% (95% CI, 53.3-90.2), and positive predictive value of 88.5% (95% CI, 76.6-95.7). The galanin expression level was significantly increased with tumor size and tumor stage. These findings justify a prospective assessment of serum galanin protein as a screening tool for colon cancer. (Cancer Epidemiol Biomarkers Prev 2007;16(11):2373–8)
This article has been cited by other articles:
![]() |
R. A. Mentor-Marcel, G. Bobe, K. G. Barrett, M. R. Young, P. S. Albert, M. R. Bennink, E. Lanza, and N. H. Colburn Inflammation-Associated Serum and Colon Markers as Indicators of Dietary Attenuation of Colon Carcinogenesis in ob/ob Mice Cancer Prevention Research, January 1, 2009; 2(1): 60 - 69. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Lage, N. T. Hansen, E. O. Karlberg, A. C. Eklund, F. S. Roque, P. K. Donahoe, Z. Szallasi, T. S. Jensen, and S. Brunak A large-scale analysis of tissue-specific pathology and gene expression of human disease genes and complexes PNAS, December 30, 2008; 105(52): 20870 - 20875. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Cancer Research | Clinical Cancer Research |
| Cancer Epidemiology Biomarkers & Prevention | Molecular Cancer Therapeutics |
| Molecular Cancer Research | Cancer Prevention Research |
| Cancer Prevention Journals Portal | Cancer Reviews Online |
| Annual Meeting Education Book | Meeting Abstracts Online |