Noncytotoxic and Sublethal Paclitaxel Treatment Potentiates the Sensitivity of Cultured Ovarian Tumor SKOV-3 Cells to Lysis by Lymphokine-activated Killer Cells

碩士 === 長庚大學 === 臨床醫學研究所 === 95 === The standard treatment of advanced epithelial ovarian cancer is tumor debulking by surgery, followed by six cycles of chemotherapy consisting of cisplatinum and paclitaxel. However, this therapy protocol is not satisfactory, since about 50% of the treated patients...

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Main Authors: LAW KIMSENG, 劉錦成
Other Authors: Prof.Shuen-Kuei Liao)
Format: Others
Language:en_US
Published: 2007
Online Access:http://ndltd.ncl.edu.tw/handle/24703372721905313876
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spelling ndltd-TW-095CGU005210022016-05-25T04:14:00Z http://ndltd.ncl.edu.tw/handle/24703372721905313876 Noncytotoxic and Sublethal Paclitaxel Treatment Potentiates the Sensitivity of Cultured Ovarian Tumor SKOV-3 Cells to Lysis by Lymphokine-activated Killer Cells 以非細胞毒殺性及未致死性劑量的紫杉醇預先處理之卵巢腫瘤細胞SKOV-3可增加被淋巴球激活殺手細胞溶解之敏感度 LAW KIMSENG 劉錦成 碩士 長庚大學 臨床醫學研究所 95 The standard treatment of advanced epithelial ovarian cancer is tumor debulking by surgery, followed by six cycles of chemotherapy consisting of cisplatinum and paclitaxel. However, this therapy protocol is not satisfactory, since about 50% of the treated patients eventually experience recurrence within few years of follow-up. Thus, a more innovative treatment modality is urgently needed for patients with this malignancy. We hypothesized that pretreatment of ovarian cancer SKOV-3 cells at a noncytotoxic to sublethal dose range of paclitaxel would result in increased sensitivity to LAK-mediated killing. MTT and trypan blue dye exclusion were used to determine the noncytotoxic to sublethal range of paclitaxel against SKOV-3 cells. A 4-h 51Cr release cytotoxicity assay was used to evaluate the sensitivity of paclitaxel-treated and untreated SKOV-3 cells. Immunofluorescence/flow cytometric analysis was used for phenotypic changes of cells with or without paclitaxel treatment. Our results with trypan blue dye exclusion and MTT assays showed that the noncytotoxic to sublethal range was between 0.001 μM and 0.01 μM. Pretreatment of SKOV-3 cells with paclitaxel at these doses for 72 h revealed significantly enhanced LAK-mediated killing against SKOV-3 cells with the highest sensitivity achieved with cells treated with 0.001 μM paclitaxel, as compared with the baseline killing of untreated cells using LAK cell alone (p<0.05). The enhanced sensitivity of LAK-mediated killing appeared to be in part due to paclitaxel-induced expression of ICAM-1 on SKOV-3 cells. This treatment approach may be useful for further development of an effective therapeutic mode for patients with ovarian cancer. Prof.Shuen-Kuei Liao) 廖順奎 2007 學位論文 ; thesis 45 en_US
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description 碩士 === 長庚大學 === 臨床醫學研究所 === 95 === The standard treatment of advanced epithelial ovarian cancer is tumor debulking by surgery, followed by six cycles of chemotherapy consisting of cisplatinum and paclitaxel. However, this therapy protocol is not satisfactory, since about 50% of the treated patients eventually experience recurrence within few years of follow-up. Thus, a more innovative treatment modality is urgently needed for patients with this malignancy. We hypothesized that pretreatment of ovarian cancer SKOV-3 cells at a noncytotoxic to sublethal dose range of paclitaxel would result in increased sensitivity to LAK-mediated killing. MTT and trypan blue dye exclusion were used to determine the noncytotoxic to sublethal range of paclitaxel against SKOV-3 cells. A 4-h 51Cr release cytotoxicity assay was used to evaluate the sensitivity of paclitaxel-treated and untreated SKOV-3 cells. Immunofluorescence/flow cytometric analysis was used for phenotypic changes of cells with or without paclitaxel treatment. Our results with trypan blue dye exclusion and MTT assays showed that the noncytotoxic to sublethal range was between 0.001 μM and 0.01 μM. Pretreatment of SKOV-3 cells with paclitaxel at these doses for 72 h revealed significantly enhanced LAK-mediated killing against SKOV-3 cells with the highest sensitivity achieved with cells treated with 0.001 μM paclitaxel, as compared with the baseline killing of untreated cells using LAK cell alone (p<0.05). The enhanced sensitivity of LAK-mediated killing appeared to be in part due to paclitaxel-induced expression of ICAM-1 on SKOV-3 cells. This treatment approach may be useful for further development of an effective therapeutic mode for patients with ovarian cancer.
author2 Prof.Shuen-Kuei Liao)
author_facet Prof.Shuen-Kuei Liao)
LAW KIMSENG
劉錦成
author LAW KIMSENG
劉錦成
spellingShingle LAW KIMSENG
劉錦成
Noncytotoxic and Sublethal Paclitaxel Treatment Potentiates the Sensitivity of Cultured Ovarian Tumor SKOV-3 Cells to Lysis by Lymphokine-activated Killer Cells
author_sort LAW KIMSENG
title Noncytotoxic and Sublethal Paclitaxel Treatment Potentiates the Sensitivity of Cultured Ovarian Tumor SKOV-3 Cells to Lysis by Lymphokine-activated Killer Cells
title_short Noncytotoxic and Sublethal Paclitaxel Treatment Potentiates the Sensitivity of Cultured Ovarian Tumor SKOV-3 Cells to Lysis by Lymphokine-activated Killer Cells
title_full Noncytotoxic and Sublethal Paclitaxel Treatment Potentiates the Sensitivity of Cultured Ovarian Tumor SKOV-3 Cells to Lysis by Lymphokine-activated Killer Cells
title_fullStr Noncytotoxic and Sublethal Paclitaxel Treatment Potentiates the Sensitivity of Cultured Ovarian Tumor SKOV-3 Cells to Lysis by Lymphokine-activated Killer Cells
title_full_unstemmed Noncytotoxic and Sublethal Paclitaxel Treatment Potentiates the Sensitivity of Cultured Ovarian Tumor SKOV-3 Cells to Lysis by Lymphokine-activated Killer Cells
title_sort noncytotoxic and sublethal paclitaxel treatment potentiates the sensitivity of cultured ovarian tumor skov-3 cells to lysis by lymphokine-activated killer cells
publishDate 2007
url http://ndltd.ncl.edu.tw/handle/24703372721905313876
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