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EXPERIMENTAL STUDY OF MECHANISM OF ANGIOGENESIS INHIBITOR, TNP-470 ON THE BONE METABOLISM AND CLINICAL APPROACH FOR HUMORAL HYPERCALCEMIA OF MARIGNANCY.

Research Project

Project/Area Number 12557175
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section展開研究
Research Field Surgical dentistry
Research InstitutionOKAYAMA UNIVERSITY

Principal Investigator

SASAKI Akira  GRADUATE SCHOOL OF MEDICINE AND DENTISTRY, OKAYAMA UNIVERSITY, ASSOCIATE PROFESSOR, 大学院・医歯学総合研究科, 助教授 (00170663)

Co-Investigator(Kenkyū-buntansha) KUSAKA Masami  TAKEDA CHEMICAL INDUSTRIES LTD, CHIEF INVESTIGATOR, 創薬研究本部創薬第二研究所, 主任研究員
MESE Hiroshi  GRADUATE SCHOOL OF MEDICINE AND DENTISTRY, OKAYAMA UNIVERSITY, INSTRUCTOR, 大学院・医歯学総合研究科, 助手 (40325098)
Project Period (FY) 2000 – 2001
Project Status Completed (Fiscal Year 2001)
Budget Amount *help
¥5,400,000 (Direct Cost: ¥5,400,000)
Fiscal Year 2001: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2000: ¥3,700,000 (Direct Cost: ¥3,700,000)
Keywordsosteoclast / oral squamous cell carsinoma / hypercalcemia / bone resorption / angiogenesis inhibitor / TNP-470 / bone disease / PTHrP / 口腟扁平上皮癌 / 血管新生障害剤
Research Abstract

Humoral hypercalcemia of malignancy (HHM) causes a decline in the quality of life of cancer patients. We previously demonstrated that the angiogenesis inhibitor, TNP-470, inhibited not only tumor growth but also oeteoclastic bone resorption. It is suggested that TNP-470 has a possibility of therapeutic use for the treatment of the HHM. In the present study, we investigated the mechanism of TNP-470 on the bone metabolism and clinical approach for HHM.
Effects of TNP-470 for hypercalcemia in vivo
We employed a hypercalcemia model using a human oral squamous cell carcinoma OCC-1 secreting PTHrP. In the therapeutic treatment, TNP-470 was administerd subcutaneously after the definition of hypercalcemia. In the prophylactic treatment, TNP-470 was given before manifestation of hypercalcemia. In both treatments, TNP-470 markedly suppressed the increase of blood Ca^<2+>. Particularly in the prophylactic treatment, TNP-470 significantly inhibited the progression of the tumor growth and prolonged t … More he survival.
In another experimental hypercalcemia model induced by PTHrP and IL-1β, TNP-470 also suppressed hypercalcemia.
Effects of angiogenesis inhibitors on osteoclasts formation in vitro
In a murine bone marrow culture under VitD_3, not only TNP-470 but also Angiostatin, Ursolic acid suppressed osteoclasts formation. However, other angiogenesis inhibitors, didn't suppress osteoclasts formation.
Mechanism of the inhibitory effects on the osteoclasts formation of TNP-470
TNP-470 suppressed osteoclasts formation, but didn't affect bone resorption activity of osteoclasts. TNP-470 didn't affect the expression of RANKL, OPG, and M-CSF mRNA in bone marrow/ stromal cells.
Inhibitory effects of cell proliferation and Cytotoxicity of TNP-470
In various types of cells, TNP-470 suppressed cell proliferation and showed cytotoxicity at a high concentration. From these results, TNP-470 didn't suppress osteoclasts formation because of cytotoxicity.
These data suggested that TNP-470, which possessed both antitumor action and osteoclast-inhibitory activity, should be a beneficial drug not only for HHM but also other cancer-induced bone diseases. Less

Report

(3 results)
  • 2001 Annual Research Report   Final Research Report Summary
  • 2000 Annual Research Report

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Published: 2000-04-01   Modified: 2016-04-21  

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