| Project/Area Number |
17591769
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Obstetrics and gynecology
|
|---|
| Research Institution | Japanese Foundation for cancer research |
|---|
Principal Investigator |
SUGIYAMA Yuko Japanese Foundation for cancer research, Genome center, Associate, ゲノムセンター, 研究員 (80322634)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
HASUMI Katsuhiko Japanese Foundation for cancer research, Cancer institute, Associate, 癌研究所, 研究員 (70134608)
|
|---|
| Project Period (FY) |
2005 – 2006
|
| Project Status |
Completed (Fiscal Year 2006)
|
| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 2006: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 2005: ¥1,200,000 (Direct Cost: ¥1,200,000)
|
|---|
| Keywords | cancer / translational research / microarray |
|---|
| Research Abstract |
Purpose : Type I endometrial cancer is accompanied by hyperplasia and type II endometrial cancer is not. The purpose of our study is to identify genes involved in carcinogenesis of endometrial cancer, especially those differentially expressed by type I and type II cancers among those surgical stages.
Experimental Design : Using a cDNA array technique (GeneChip Human Genome U133 Plus 2.0 Array), we examined expression of 38,500 genes in endometrial cancer cells sampled from 31 tumors, and we compared the expression patterns of the tumor cells with or without hyperplasia. Of these, 15 cases were type I cancers and 16 cases were type II cancers. Laser-capture microdissection directed precise separation of cells of interest from stromal cells. In cancer cells, we identified genes differentially expressed by the two types of cancers. Then hierarchical clustering was applied to those identified genes.
Results : Of 38,500 genes examined, 2760 genes were identified to have different levels (SD>1) of expression in type I and type II cancers.
|
