<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-20T00:11:40Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/34439" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/34439</identifier><datestamp>2022-01-25T17:21:05Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Jeffrey A. Coderre.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Wang, Rong, Ph. D. Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Nuclear Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department" lang="en_US">Massachusetts Institute of Technology. Department of Nuclear Engineering</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Nuclear Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2006-11-07T12:10:08Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2006-11-07T12:10:08Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2005</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/34439</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">70689908</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Nuclear Engineering, 2005.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">"September 2005."</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The objective of this project is to establish a model system to study the direct effect, the bystander effect and the combinational effect of alpha-particle irradiations of human prostate tumor cells, toward the goal of improving the effectiveness of alpha-particle involved radiation therapies such as radioimmunotherapy and BNCT. This project consists of an engineering part and a biological part. In the engineering part, an apparatus for alpha-particle irradiation of cells was designed and constructed. Dosimetry of this irradiator was conducted. The average dose rate to the cell monolayer in the specially designed Mylar dish was calculated to be 1.2 Gy/min. In the biological part, three in vitro studies were carried out with the DU-145 human prostate tumor cells using the established alpha-particle irradiator. Firstly, the direct effects of the alpha-particle irradiation of DU-145 cells were studied using the clonogenic assay, the comet assay and the micronucleus assay. A novel co-culture system was then designed to study the bystander effect transmitted through the cell culture medium. The micronucleus assay was used as endpoint for the bystander studies. A bystander effect was observed.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">(cont.) Mechanism studies suggested that the nitric oxide was not involved in the process and indicated a short effective lifetime (&lt; min) of the bystander signal. In the combinational studies, the effects of two anticancer drugs (Taxol and Oxaliplatin) together with direct alpha-particle irradiation were studied and no synergistic effect was observed for both drugs. Finally, the combined effect of the bystander effect and drug Taxol was studied, which was the first time that a combined effect between an anticancer drug and the radiation-induced bystander effect was studied. The results of the model studies carried out in the two-dimensional monolayer of cells in this project can serve as a fundamental frame to be further applied to a three dimensional tumor micrometastasis model (spheroids) in the future. The understanding of the role the bystander effect plays in tumor cell killing, its mechanisms and its interaction with other agents, may make it possible to manipulate these factors to improve the effectiveness of alpha-particle involved therapies.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Rong Wang.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
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   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Nuclear Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Direct and indirect effects of alpha-particle irradiations of human prostate tumor cells</dim:field>
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   	&lt;Title>Direct and indirect effects of alpha-particle irradiations of human prostate tumor cells&lt;/Title>
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   	&lt;PublicationDate>2005&lt;/PublicationDate>
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        	&lt;DisplayName>Wang, Rong, Ph. D. Massachusetts Institute of Technology&lt;/DisplayName>
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    &lt;Keyword>Nuclear Engineering.&lt;/Keyword>
   	&lt;Abstract>The objective of this project is to establish a model system to study the direct effect, the bystander effect and the combinational effect of alpha-particle irradiations of human prostate tumor cells, toward the goal of improving the effectiveness of alpha-particle involved radiation therapies such as radioimmunotherapy and BNCT. This project consists of an engineering part and a biological part. In the engineering part, an apparatus for alpha-particle irradiation of cells was designed and constructed. Dosimetry of this irradiator was conducted. The average dose rate to the cell monolayer in the specially designed Mylar dish was calculated to be 1.2 Gy/min. In the biological part, three in vitro studies were carried out with the DU-145 human prostate tumor cells using the established alpha-particle irradiator. Firstly, the direct effects of the alpha-particle irradiation of DU-145 cells were studied using the clonogenic assay, the comet assay and the micronucleus assay. A novel co-culture system was then designed to study the bystander effect transmitted through the cell culture medium. The micronucleus assay was used as endpoint for the bystander studies. A bystander effect was observed.&lt;/Abstract>
   	&lt;Abstract>(cont.) Mechanism studies suggested that the nitric oxide was not involved in the process and indicated a short effective lifetime (&amp;lt; min) of the bystander signal. In the combinational studies, the effects of two anticancer drugs (Taxol and Oxaliplatin) together with direct alpha-particle irradiation were studied and no synergistic effect was observed for both drugs. Finally, the combined effect of the bystander effect and drug Taxol was studied, which was the first time that a combined effect between an anticancer drug and the radiation-induced bystander effect was studied. The results of the model studies carried out in the two-dimensional monolayer of cells in this project can serve as a fundamental frame to be further applied to a three dimensional tumor micrometastasis model (spheroids) in the future. The understanding of the role the bystander effect plays in tumor cell killing, its mechanisms and its interaction with other agents, may make it possible to manipulate these factors to improve the effectiveness of alpha-particle involved therapies.&lt;/Abstract>
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