The Study of IL-20 in Cancer-Induced Osteolysis

碩士 === 國立成功大學 === 生物化學暨分子生物學研究所 === 102 === Cancer is the most common disease in the world. It may also spread to distant parts of the body and increase the mortality. Bone is one of the site for cancer metastasis. Cancer cells in the bone reduce bone mineral density and induce pain in patients. IL-...

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Main Authors: Cheng-YingWu, 吳承穎
Other Authors: Ming-Shi Chang
Format: Others
Language:zh-TW
Published: 2014
Online Access:http://ndltd.ncl.edu.tw/handle/9cf4x6
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spelling ndltd-TW-102NCKU51040522019-05-15T21:42:46Z http://ndltd.ncl.edu.tw/handle/9cf4x6 The Study of IL-20 in Cancer-Induced Osteolysis 介白素二十在癌症骨侵蝕中的研究 Cheng-YingWu 吳承穎 碩士 國立成功大學 生物化學暨分子生物學研究所 102 Cancer is the most common disease in the world. It may also spread to distant parts of the body and increase the mortality. Bone is one of the site for cancer metastasis. Cancer cells in the bone reduce bone mineral density and induce pain in patients. IL-20 is a cytokine belonging to the IL-10 family. IL-20 binds to a heterodimer receptor complex IL-20R1/IL-20R2 mediating its signal transduction. Previous studies showed that IL-20 is involved in several diseases, such as psoriasis, rheumatoid arthritis and cancer. In our previous study, anti-IL-20 monoclonal antibody 7E suppressed breast cancer-induced osteolysis. To investigate whether 7E can suppress other cancer cells-induced osteolysis, we used five different kinds of cancers: prostate cancer, esophageal cancer, oral cancer, osteosarcoma and multiple myeloma to establish cancer-induced osteolysis animal models. Our result showed that 7E suppressed prostate cancer and esophageal cancer induced osteolysis. However, 7E did not suppress osteolysis in oral cancer, osteosarcoma and multiple myeloma. Furthermore, IL-20 increased gene expression of sRANKL, cathepsin G and cathepsin K and sRANKL protein expression in prostate cancer cell. Condition medium of prostate cancer cell suppressed pre-osteoblast proliferation. 7E also suppressed prostate cancer cell proliferation, migration and colony formation. IL-20 also induced phosphorylation of P-38, Erk1/2, Akt and NFκB in prostate cancer cell. In addition, IL-20 upregulated STAT3, vimentin, fibronectin and N-cadherin gene expression. 7E also suppressed esophageal cancer cell proliferation, migration and colony formation. Our study provides the evidence that 7E has a protective function in prostate and esophageal cancer-induced osteolysis in animal model and anti-IL-20 monoclonal antibody 7E may have therapeutic potential in cancer-induced osteolysis. Ming-Shi Chang 張明熙 2014 學位論文 ; thesis 68 zh-TW
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description 碩士 === 國立成功大學 === 生物化學暨分子生物學研究所 === 102 === Cancer is the most common disease in the world. It may also spread to distant parts of the body and increase the mortality. Bone is one of the site for cancer metastasis. Cancer cells in the bone reduce bone mineral density and induce pain in patients. IL-20 is a cytokine belonging to the IL-10 family. IL-20 binds to a heterodimer receptor complex IL-20R1/IL-20R2 mediating its signal transduction. Previous studies showed that IL-20 is involved in several diseases, such as psoriasis, rheumatoid arthritis and cancer. In our previous study, anti-IL-20 monoclonal antibody 7E suppressed breast cancer-induced osteolysis. To investigate whether 7E can suppress other cancer cells-induced osteolysis, we used five different kinds of cancers: prostate cancer, esophageal cancer, oral cancer, osteosarcoma and multiple myeloma to establish cancer-induced osteolysis animal models. Our result showed that 7E suppressed prostate cancer and esophageal cancer induced osteolysis. However, 7E did not suppress osteolysis in oral cancer, osteosarcoma and multiple myeloma. Furthermore, IL-20 increased gene expression of sRANKL, cathepsin G and cathepsin K and sRANKL protein expression in prostate cancer cell. Condition medium of prostate cancer cell suppressed pre-osteoblast proliferation. 7E also suppressed prostate cancer cell proliferation, migration and colony formation. IL-20 also induced phosphorylation of P-38, Erk1/2, Akt and NFκB in prostate cancer cell. In addition, IL-20 upregulated STAT3, vimentin, fibronectin and N-cadherin gene expression. 7E also suppressed esophageal cancer cell proliferation, migration and colony formation. Our study provides the evidence that 7E has a protective function in prostate and esophageal cancer-induced osteolysis in animal model and anti-IL-20 monoclonal antibody 7E may have therapeutic potential in cancer-induced osteolysis.
author2 Ming-Shi Chang
author_facet Ming-Shi Chang
Cheng-YingWu
吳承穎
author Cheng-YingWu
吳承穎
spellingShingle Cheng-YingWu
吳承穎
The Study of IL-20 in Cancer-Induced Osteolysis
author_sort Cheng-YingWu
title The Study of IL-20 in Cancer-Induced Osteolysis
title_short The Study of IL-20 in Cancer-Induced Osteolysis
title_full The Study of IL-20 in Cancer-Induced Osteolysis
title_fullStr The Study of IL-20 in Cancer-Induced Osteolysis
title_full_unstemmed The Study of IL-20 in Cancer-Induced Osteolysis
title_sort study of il-20 in cancer-induced osteolysis
publishDate 2014
url http://ndltd.ncl.edu.tw/handle/9cf4x6
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