| Project/Area Number |
11557064
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 展開研究 |
|---|
| Research Field |
Dermatology
|
|---|
| Research Institution | Shinshu University School of Nedicine |
|---|
Principal Investigator |
SAIDA Toshiaki Shinshu Univ., School of Med, Prof., 医学部, 教授 (10010381)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
YOSHIDA Jun Nagoya Univ. Graduate School of Med. Prof., 大学院・医学研究科, 教授 (40158449)
KUBO Hitomi Shinshu Univ. School of Med, Assistant, 医学部, 助手 (60234481)
MATSUMOTO Kazuhiko Shinshu Univ. School of Med, Assistant Prof., 医学部, 講師 (40165882)
KAGESHITA Toshiro Kumamoto Univ., School of Med, Associate Prof., 医学部, 助教授 (20152605)
MIZUNO Masaaki Nagoya Univ. Graduate School of Med. Associate Prof., 大学院・医学研究科, 助教授 (70283439)
|
|---|
| Project Period (FY) |
1999 – 2001
|
| Project Status |
Completed (Fiscal Year 2001)
|
| Budget Amount *help |
¥13,200,000 (Direct Cost: ¥13,200,000)
Fiscal Year 2001: ¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2000: ¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 1999: ¥6,400,000 (Direct Cost: ¥6,400,000)
|
|---|
| Keywords | Malignant melanoma / Gene therapy / Interferon-β / Liposome |
|---|
| Research Abstract |
The purpose of this project is to develop a new gene therapy for patients with advanced malignant melanoma, which is highly resistant to any conventional therapies. In our previous study, we found that malignant melanoma transfected with interferon-β( IFN-β ) gene by means of cationic multilamellar liposomes expressed the gene and secreted IFN-β. Moreover, human melanoma nodules transplanted to nude mice were eradicated completely with 6 times injection of IFN-β gene ( 3ug DNA/time ). This year, we have investigated mechanisms of effect of this gene therapy. We have found transfection of IFN-β gene induces apoptosis of melanoma cells. In addition, in experiments in the murine B16 melanoma system, we have found NK cells play an important role in the growth inhibition ofmelanoma nodules in C57BL/6 mice. Furthermore, we have confirmed repeated treatment with the cationic liposome containing IFN-β gene increases tranfection efficiency of the gene.
Based on the data obtained in studies in this year along with those performed in the previous 2 years, we consider we have almost completely finished preparation for the clinical study. We have now applied clinical trial of this gene therapy to the committees of our medical school in order to start the clinical study of the gene therapy for patients with advanced melanoma.
|
