Abstract |
The purpose of this study was to screen for genes involved in ovarian carcinogenesis in an attempt to develop an effective molecular-targeted therapy for ovarian cancer. We constructed retroviral expression libraries for the human ovarian cancer cell lines SHIN-3 and TYK- CPr, and performed a focus formation assay with 3T3 cells. As a result, proteasome subunit beta-type 2 (PSMB2), ubiquitin-specific protease 14 (USP14), and keratin 8 (KRT8) were identified from SHIN-3, and polymerase II RNA subunit (POLR2E), chaperonin containing T-complex polypeptide 1 subunit 4 (CCT4), glia maturation factor beta (GMFB), and neuroblastoma ras viral oncogene homolog (NRAS) from TYK- CPr. NRAS gene analysis revealed a CAA --> AAA substitution at codon 61, resulting in a Glu --> Lys change at position 61. When the mutant NRAS was introduced into fibroblasts for its expression, many transformed foci were generated, confirming the transforming ability of the mutant NRAS.
|
Authors | Tomoaki Wada, Yoshihiro Yamashita, Yasushi Saga, Kayoko Takahashi, Koji Koinuma, Young Lim Choi, Ruri Kaneda, Shin-Ichiro Fujiwara, Manabu Soda, Hideki Watanabe, Kentaro Kurashina, Hisashi Hatanaka, Munehiro Enomoto, Shuji Takada, Hiroyuki Mano, Mitsuaki Suzuki |
Journal | International journal of oncology
(Int J Oncol)
Vol. 35
Issue 5
Pg. 973-6
(Nov 2009)
ISSN: 1791-2423 [Electronic] Greece |
PMID | 19787249
(Publication Type: Journal Article)
|
Topics |
- Amino Acid Sequence
- Animals
- Base Sequence
- Cell Line, Tumor
- Female
- Gene Library
- Genes, ras
(genetics)
- Genetic Testing
(methods)
- Humans
- Mice
- Molecular Sequence Data
- Ovarian Neoplasms
(genetics)
- Retroviridae
(genetics)
- Reverse Transcriptase Polymerase Chain Reaction
|