Expression pattern of the class I homeobox genes in ovarian carcinoma
- Authors
- Hong, Jin Hwa; Lee, Jae Kwan; Park, Joong Jean; Lee, Nak Woo; Lee, Kyu Wan; Na, Jung Yeol
- Issue Date
- 3월-2010
- Publisher
- KOREAN SOC GYNECOLOGY ONCOLOGY & COLPOSCOPY
- Keywords
- Homeobox gene; Ovarian neoplasms; Carcinogenesis
- Citation
- JOURNAL OF GYNECOLOGIC ONCOLOGY, v.21, no.1, pp.29 - 37
- Indexed
- SCIE
SCOPUS
KCI
OTHER
- Journal Title
- JOURNAL OF GYNECOLOGIC ONCOLOGY
- Volume
- 21
- Number
- 1
- Start Page
- 29
- End Page
- 37
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/134476
- DOI
- 10.3802/jgo.2010.21.1.29
- ISSN
- 2005-0380
- Abstract
- Objective: Although some sporadic reports reveal the link between the homeobox (HOX) genes and ovarian carcinoma, there is no comprehensive analysis of the expression pattern of the class 1 homeobox genes in ovarian carcinoma that determines the candidate genes involved in ovarian carcinogenesis. Methods: The different patterns of expression of 36 HOX genes were analyzed, including 4 ovarian cancer cell lines and 4 normal ovarian tissues. Using a reverse transcription-polymerase chain reaction (RT-PCR) and quantification analysis, the specific gene that showed a significantly higher expression in ovarian cancer cell lines than in normal ovaries was selected, and western blot analysis was performed adding 7 ovarian cancer tissue specimens. Finally, immunohistochemical and immunocytochemical analyses were performed to compare the pattern of expression of the specific HOX gene between ovarian cancer tissue and normal ovaries. Results: Among 36 genes, 11 genes had a different level of mRNA expression between the cancer cell lines and the normal ovarian tissues. Of the 11 genes, only HOXB4 had a significantly higher level of expression in ovarian cancer cell lines than in normal ovaries (p=0.029). Based on western blot, immunohistochemical, and immunocytochemical analyses, HOXB4 was expressed exclusively in the ovarian cancer cell lines or cancer tissue specimens, but not in the normal ovaries. Conclusion: We suggest HOXB4 may be a novel candidate gene involved in ovarian carcinogenesis.
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