Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)

Includes bibliographical references (leaves 50-53).

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Kasbo, Zein Jean (author)
التنسيق: masterThesis
منشور في: 2014
الموضوعات:
الوصول للمادة أونلاين:http://hdl.handle.net/10725/1971
https://doi.org/10.26756/th.2014.40
الوسوم: إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
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author Kasbo, Zein Jean
author_facet Kasbo, Zein Jean
author_role author
dc.creator.none.fl_str_mv Kasbo, Zein Jean
dc.date.none.fl_str_mv 2014-07-22
2015-02-26T07:18:28Z
2015-02-26T07:18:28Z
2015-02-26
dc.identifier.none.fl_str_mv http://hdl.handle.net/10725/1971
https://doi.org/10.26756/th.2014.40
dc.language.none.fl_str_mv en
dc.publisher.none.fl_str_mv Lebanese American University
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Colon (Anatomy) -- Cancer -- Treatment
Rectum -- Cancer -- Treatment
Bacillus anthracis -- Toxicology
Anthrax
Urokinase -- Therapeutic use
Lebanese American University -- Dissertations
Dissertations, Academic
dc.title.none.fl_str_mv Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)
dc.type.none.fl_str_mv Thesis
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/masterThesis
description Includes bibliographical references (leaves 50-53).
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language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/1971
publishDate 2014
publisher.none.fl_str_mv Lebanese American University
repository.mail.fl_str_mv
repository.name.fl_str_mv
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spelling Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)Kasbo, Zein JeanColon (Anatomy) -- Cancer -- TreatmentRectum -- Cancer -- TreatmentBacillus anthracis -- ToxicologyAnthraxUrokinase -- Therapeutic useLebanese American University -- DissertationsDissertations, AcademicIncludes bibliographical references (leaves 50-53).In this study, we attempt to simultaneously target the major hallmarks of colorectal cancer (CRC), the MAPK pathway and the urokinase plasminogen activator system using a dual-selective, Urokinase-activated, recombinant anthrax lethal toxin (PrAgU2/LF). Colorectal cancer is the third most common cancer type in the world, and the second leading cause of death in the United States according to the American cancer society. Therefore, the need for alternative approaches is essential in order to overcome the difficulties faced with traditional therapies. PrAgU2/LF is composed of 2 components the binding moiety PrAgU2 and the catalytic moiety LF. PrAgU2 was obtained by replacing the furin cleavage sequence on PrAg with a urokinase- specific cleavage sequence. LF is a metalloprotease that cleaves and inactivates MEKs and hence inhibits the MAPK pathway. We assessed the cytotoxic effects and mechanisms of PrAgU2/LF on a panel of 9 human colorectal cancer cell lines.PrAg/LF, PrAg/FP59 and PrAgU2/FP59 were used as controls for the different components of this system. PrAgU2/LF was not significantly cytotoxic to any of the cell lines tested, which were also resistant to PrAg/LF, indicating resistance to the inhibition of the MAPK pathway. This was further confirmed by resistance of these cells to the MEK1/2 inhibitor U0126. Notably, the majority of cell lines showed high levels of phospho-MEK1/2 but, surprisingly, no phospho-ERK1/2. Furthermore, targeting both the MAPK pathway and the PI3-kinase/Akt pathway also failed to induce cytotoxicity in colon cancer cell lines. In order to assess the possibility of targeting the uPA/uPAR system alone, we determined expression levels of uPAR and tested the sensitivity of CRC cells to PrAgU2/FP59, a urokinase activated, MAPK-independent version of the toxin. The vast majority of cell lines tested expressed uPAR and were sensitive to PrAgU2/FP59, indicating the possibility for targeting this protease system in CRC.1 hard copy: xv, 53 leaves; col. ill.; 30 cm. available at RNL.Lebanese American University2015-02-26T07:18:28Z2015-02-26T07:18:28Z2015-02-262014-07-22Thesisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesishttp://hdl.handle.net/10725/1971https://doi.org/10.26756/th.2014.40eninfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/19712020-05-18T14:53:56Z
spellingShingle Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)
Kasbo, Zein Jean
Colon (Anatomy) -- Cancer -- Treatment
Rectum -- Cancer -- Treatment
Bacillus anthracis -- Toxicology
Anthrax
Urokinase -- Therapeutic use
Lebanese American University -- Dissertations
Dissertations, Academic
status_str publishedVersion
title Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)
title_full Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)
title_fullStr Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)
title_full_unstemmed Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)
title_short Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)
title_sort Sensitivity of colorectal cancer cells to the recombinant Anthrax lethal toxin and the Urokinase-activated Anthrax lethal toxin. (c2014)
topic Colon (Anatomy) -- Cancer -- Treatment
Rectum -- Cancer -- Treatment
Bacillus anthracis -- Toxicology
Anthrax
Urokinase -- Therapeutic use
Lebanese American University -- Dissertations
Dissertations, Academic
url http://hdl.handle.net/10725/1971
https://doi.org/10.26756/th.2014.40