Selection of The Potential Anti-prostate Cancer Drugs and Gene

碩士 === 嘉南藥理大學 === 生物科技系 === 105 === Prostate cancer is one of the top ten cancer causes in the Ministry of Health department of Taiwan's statistics, and the second major cause of male cancer death in 2016 on the United States. The risk of having prostate cancer will increase with the age. Prost...

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Main Authors: Zhang, Cheng-Yu, 張澄羽
Other Authors: Hung, Jui-Hsiang
Format: Others
Language:zh-TW
Published: 2017
Online Access:http://ndltd.ncl.edu.tw/handle/zpx384
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spelling ndltd-TW-105CNUP01110072019-05-15T23:32:34Z http://ndltd.ncl.edu.tw/handle/zpx384 Selection of The Potential Anti-prostate Cancer Drugs and Gene 尋找具抑制前列腺癌的潛力藥物及基因 Zhang, Cheng-Yu 張澄羽 碩士 嘉南藥理大學 生物科技系 105 Prostate cancer is one of the top ten cancer causes in the Ministry of Health department of Taiwan's statistics, and the second major cause of male cancer death in 2016 on the United States. The risk of having prostate cancer will increase with the age. Prostate cancer treatments are mainly included surgical resection, radiation therapy, cryotherapy and hormonal treatment, but we still need to find more effective treatments and drugs for against the population aging and mortality. In this study, we analyze the potential target gene by using bioinformatics and focus on research the potential drugs. In the bioinformatics analysis, overexpression of PDLIM5 in prostate cancer was determined by using Oncomine database. In addition, poor survival rate in PDLIM5 overexpression prostate cancer patients were observed form Survnexpress, PROGeneV2, PrognoScan and Cancer Cell Line Encyclopedia (CCLE) database. We analyzed 27 compounds and the results showed that compound No. 7 had better effects on prostate cancer cell lines LNCaP and PC-3 cells. Therefore, in the further study, we will try to investigate the signaling pathways of compound No. 7 and the role of PDLIM5 in prostate cancer cells. These results will be helpful on developing the potential drugs. Hung, Jui-Hsiang 洪瑞祥 2017 學位論文 ; thesis 72 zh-TW
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description 碩士 === 嘉南藥理大學 === 生物科技系 === 105 === Prostate cancer is one of the top ten cancer causes in the Ministry of Health department of Taiwan's statistics, and the second major cause of male cancer death in 2016 on the United States. The risk of having prostate cancer will increase with the age. Prostate cancer treatments are mainly included surgical resection, radiation therapy, cryotherapy and hormonal treatment, but we still need to find more effective treatments and drugs for against the population aging and mortality. In this study, we analyze the potential target gene by using bioinformatics and focus on research the potential drugs. In the bioinformatics analysis, overexpression of PDLIM5 in prostate cancer was determined by using Oncomine database. In addition, poor survival rate in PDLIM5 overexpression prostate cancer patients were observed form Survnexpress, PROGeneV2, PrognoScan and Cancer Cell Line Encyclopedia (CCLE) database. We analyzed 27 compounds and the results showed that compound No. 7 had better effects on prostate cancer cell lines LNCaP and PC-3 cells. Therefore, in the further study, we will try to investigate the signaling pathways of compound No. 7 and the role of PDLIM5 in prostate cancer cells. These results will be helpful on developing the potential drugs.
author2 Hung, Jui-Hsiang
author_facet Hung, Jui-Hsiang
Zhang, Cheng-Yu
張澄羽
author Zhang, Cheng-Yu
張澄羽
spellingShingle Zhang, Cheng-Yu
張澄羽
Selection of The Potential Anti-prostate Cancer Drugs and Gene
author_sort Zhang, Cheng-Yu
title Selection of The Potential Anti-prostate Cancer Drugs and Gene
title_short Selection of The Potential Anti-prostate Cancer Drugs and Gene
title_full Selection of The Potential Anti-prostate Cancer Drugs and Gene
title_fullStr Selection of The Potential Anti-prostate Cancer Drugs and Gene
title_full_unstemmed Selection of The Potential Anti-prostate Cancer Drugs and Gene
title_sort selection of the potential anti-prostate cancer drugs and gene
publishDate 2017
url http://ndltd.ncl.edu.tw/handle/zpx384
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