Specific overexpression of OLFM4 GW112/hGC−1 mRNA in colon, breast and lung cancer tissues detected using quantitative analysis

Overexpression of the olfactomedin 4 ( OLFM4 GW112,/hGC−1 ) gene was recently reported to inhibit various apoptotic pathways and promote proliferation of cancer cells, suggesting that OLFM4 might serve as a diagnostic marker for human cancers. Therefore, we examined cancer‐specific OLFM4 overexpress...

Full description

Saved in:
Bibliographic Details
Published inCancer science Vol. 98; no. 3; pp. 315 - 320
Main Authors Koshida, Saori, Kobayashi, Daisuke, Moriai, Ryosuke, Tsuji, Naoki, Watanabe, Naoki
Format Journal Article
LanguageEnglish
Published 10.03.2007
Online AccessGet full text

Cover

Loading…
More Information
Summary:Overexpression of the olfactomedin 4 ( OLFM4 GW112,/hGC−1 ) gene was recently reported to inhibit various apoptotic pathways and promote proliferation of cancer cells, suggesting that OLFM4 might serve as a diagnostic marker for human cancers. Therefore, we examined cancer‐specific OLFM4 overexpression. OLFM4 mRNA was highly expressed in cancerous tissues obtained from the colon, breast and lung. Positivity for OLFM4 mRNA, defined as the mean + 2 SD in non‐cancerous colon and breast tissues, was observed in 68 and 50% of the studied colon and breast cancer tissues. OLFM4 mRNA expression was not detected in non‐cancerous lung tissues but was evident in 62% of the lung cancer tissues. On comparing paired samples, the expression of OLFM4 mRNA was observed to be elevated in 90, 69 and 85% of colon, breast and lung cancer tissues, respectively. OLFM4 mRNA expression was observed even in the early stages of each cancer type. The expression of OLFM4 mRNA did not correlate with that of the antiapoptotic molecule survivin, indicating that it can be used independently in cancer diagnosis. Combining OLFM4 and survivin resulted in higher positivity. Thus, OLFM4 mRNA might be a useful tool to support the diagnosis of cancer, irrespective of the clinical stages. ( Cancer Sci 2007; 98: 315–320)
ISSN:1347-9032
1349-7006
DOI:10.1111/j.1349-7006.2006.00383.x