| Project/Area Number |
05454360
|
|---|
| Research Category |
Grant-in-Aid for General Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
General surgery
|
|---|
| Research Institution | Yokohama City University |
|---|
Principal Investigator |
MATSUMOTO Akihiko Yokohama City University School of Medicine Professor, 医学部, 教授 (20045975)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
SATO Shinobu Yokohama City University School of Medicine, Assistant Professor, 医学部, 講師 (80244424)
ITO Takaaki Yokohama City University School of Medicine, Assistant Professor, 医学部, 講師 (70168392)
NOGUCHI Yoshikazu Yokohama City University School of Medicine, Assistant Professor, 医学部, 講師 (50180724)
|
|---|
| Project Period (FY) |
1993 – 1994
|
| Project Status |
Completed (Fiscal Year 1994)
|
| Budget Amount *help |
¥6,900,000 (Direct Cost: ¥6,900,000)
Fiscal Year 1994: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 1993: ¥5,200,000 (Direct Cost: ¥5,200,000)
|
|---|
| Keywords | insulin resistance / glucose transporter / glucose clamp / 癌悪液質 / インスリンレジスタンス / グリコーストランスポーター / euglycemic clamp |
|---|
| Research Abstract |
This study was conducted to elucidate the mechanisms of insulin resistance, observed in the tumor-bearing hosts by investigating insulin-dependent glucose transporter. Specific questions raised were 1. to elucidate insulin resistance in cancer patients and 2. clarify the role of glucose transporters in inducing cancer cachexia.
Results
1. We have examined 50 cases of cancer patients by englycemic hyperinsulinemic glucose clamp technique and insulin resistance was documented in most of those cases. This was not related with either stage of the disease nor degree of weight loss but was tumor-depended changes.
2. In Fisher rat with MCA sarcoma, glucose transport activity was significantly decreased in tumor-bearing rats compared with pair-fed control. Decrease in GLUT4 was due to decreased intracytoplasmic pool of this protein and decreased translocation to the membrane.
3. GLUT4 was demonstrated in 25% of human cancer specimens. This was not related with degree of peripheral insulin resistance. Forced administration of insulin and nutrients in those patients may facilitate tumor growth without helping nutrition of the host.
|
