4.7 Article

Clinical Significance of Human Kallikrein7 Gene Expression in Colorectal Cancer

Journal

ANNALS OF SURGICAL ONCOLOGY
Volume 17, Issue 11, Pages 3037-3042

Publisher

SPRINGER
DOI: 10.1245/s10434-010-1132-y

Keywords

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Funding

  1. Japan Society for the Promotion of Science (JSPS) [17109013, 18659384, 18390367, 18590333, 19591509, 19390336, 20390360, 20591547, 20790961, 20659209, 20790960]
  2. The Ministry of Education, Culture, Sports, Science, and Technology (MEXT) [18015039]
  3. Third-Term Comprehensive 10-year Strategy for Cancer Control [16271201]
  4. CREST
  5. Japan Science and Technology Agency (JST)
  6. NEDO (New Energy and Industrial Technology Development Organization) Technological Development for Chromosome Analysis
  7. The Ministry of Education, Culture, Sports, Science, and Technology of Japan
  8. Cancer Translational Research Project, Japan
  9. Clinical Research Foundation
  10. Grants-in-Aid for Scientific Research [20790961, 20659209, 19591509] Funding Source: KAKEN

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Background. The human kallikrein-related peptidases (KLK) are considered important prognostic biomarkers in cancer. The aim of the current study is to demonstrate gene expression of KLK7 in colorectal cancer (CRC) and to correlate the relative KLK7 expression level with clinicopathological factors of CRC. Methods. KLK7 messenger RNA (mRNA) expression was examined in nine CRC cancer cell lines by real-time polymerase chain reaction. The expression levels of KLK7 mRNA in cancerous tissues (n = 136) and paired normal tissues (n = 136) of CRC patients were also examined. Results. Six of the nine cell lines expressed the KLK7 gene. KLK7 mRNA expression levels in cancer tissues were significantly higher than those in normal tissues. Multivariate analysis revealed that the KLK7 mRNA expression level in cancer was an independent prognostic factor, especially in liver metastasis. Conclusions. We provide evidence suggesting that KLK7 mRNA expression is correlated with prognosis in CRC patients, especially in liver metastasis.

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