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1997 Fiscal Year Final Research Report Summary

Analysis for an ovarian cancer-derived factor which decreases the expression of alpha-smooth muscle actin in stromal cells

Research Project

Project/Area Number 08671901
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Obstetrics and gynecology
Research InstitutionKyushu University

Principal Investigator

KOBAYASHI Hiroaki  Kyushu Univ., Faculty of Medicine, Lecturer, 医学部, 助手 (70260700)

Co-Investigator(Kenkyū-buntansha) KAMURA Toshiharu  Kyushu Univ., Faculty of Medicine, Associate Professor, 医学部, 助教授 (30152870)
KAKU Tunchisa  Kyushu Univ., Faculty of Medicine, Senior Lecturer, 医学部, 講師 (60185717)
TANIGUCHI Shu'nichiro  Shinshu Univ., Faculty of Medicine, Professor, 医学部, 教授 (60117166)
SAITO Toshiaki  Kyushu Univ., Faculty of Medicine, Senior Lecturer, 医学部, 講師 (80162212)
Project Period (FY) 1996 – 1997
KeywordsOvarian cancer / alpha-smooth muscle actin / PDGF / Cell-cell interaction
Research Abstract

We previously reported that both the conditioned mcdium (CM) of human ovarian cancer cell lines and the malignant ovarian tumor fluid reduced the expression of alpha-smooth muscle actin (alpha-SMA) in fibroblasts. ln this study, we confirmed the inhibitory effect existed in tumor fluid of malignant ovarian tumors but not that of benign ones by using a Western blot analysis. Ovarian cancer fluid-induced inhibition was partially blocked by a neutralizing antibody against platelet-devived growth factor (PDGF) in a dose-dependent fashion. On the other hand, the effect of benign ovarian tumor fluid was unchanged by adding the PDGF antibody. We next checked whether the CMs of human ovarian cancer cell lines contained PDGF or not by using an ELISA system. All of 9 epithelial originated cancer cell lines released PDGF into their culture media and one non-epithelial originated line did not. Although almost all of benign tumors did not contain PDGF in their tumor fluid, 80% of cancers contained relatively high levels of PDGF.Thus, PDGF released by ovarian cancer cells is thought to decrease the expression of alpha-SMA in surrounding stromal cells. alpha-SMA is a cytoskeletal protein expressed not only in stromal fibroblasts but also in the cells consisting in the vessel wall. If a decrease in alpha-SMA expression results in the enhancement of tumor cell invasion into stroma, it is possible that the cancer-derived PDGF,sis-oncogene product, has the role of enhancer of tumor invasion.

  • Research Products

    (7 results)

All Other

All Publications (7 results)

  • [Publications] Masao Okadome 他: "An attempt to generate an antitumor effect in the regional lymph nodes against endometrial cancer cells by inducing artitumor cytokines" Cancer Letters. 104. 55-61 (1996)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tsunehisa Kaku 他: "Early adenocarcinoma of the uterine cerix" Gynecologic Oncology. 65. 281-285 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tsunehisa Kaku 他: "Argiogenesis in Endometrial Carcinoma" Cancer. 80. 741-747 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Saito et al.: "Antiproliferative lymphokine production by human peripheral blood lymphocytes and lymph node detected by a modified double layr soft agarose clonogenic assay." Lymphokine and Cytokine Research. 13. 55-62 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H.Kobayashi et al.: "Variant sublines of early-stage human melanomas selected for tumorigenicity in nude mice express a multicytokine-resistant phenotype." Am.J.Pathol.144. 776-786 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Sugihara et al.: "The promotion of invasion through the basement membrane of cervical carcinoma cells by fibronectin as a chemoattractant." Cancer.Lett.79. 167-173 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Sonoda et al.: "Establishment of a new human uterine cervical adenocarcinoma cell line, SiSo, and its reactivity to anti-cancer reagents." Int.J.Oncology. 6. 1099-1104 (1995)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1999-03-16  

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