Characterization of Protein Kinase C in Cisplatin Sensitive and Resistant Human Cervical Cancer HeLa Cells
dc.contributor.advisor | Basu, Alakananda | |
dc.contributor.committeeMember | Simecka, Jerry | |
dc.contributor.committeeMember | Dimitrijevich, Dan | |
dc.creator | Mohanty, Sanghamitra | |
dc.date.accessioned | 2019-08-22T19:31:26Z | |
dc.date.available | 2019-08-22T19:31:26Z | |
dc.date.issued | 2000-12-01 | |
dc.date.submitted | 2014-03-18T14:12:05-07:00 | |
dc.description.abstract | Mohanty, S., Characterization of protein kinase C in cisplatin sensitive and resistant human cervical cancer HeLa cells. Master of Science (Microbiology and Immunology), December, 2000. 37 pp., 11 illustrations, bibliography, 27 titles. Signal transduction plays a crucial role in carcinogenesis. A defect in signaling, by evading cell death or promoting cell proliferation, may result in neoplastic transformation or protection of cells from the cytotoxicity of anticancer drugs. Therefore, in order to understand the complex mechanism of drug resistance, it is relevant to probe into the important signal transduction pathways. Protein kinase C, a key signal transducer, influences cisplatin sensitivity in many cell lines. We examined whether or not the PKC signal transduction pathway is affected during development of resistance to cisplatin by tumor cells. PKC activators increased cisplatin sensitivity in both parental and cisplatin-resistant cells. Western blot analysis showed a slight decrease in cPKCα and nPKCε, an evaluation in nPKCδ and no change in the abundance of PKCϚ in HeLa/CP cells compared to HeLa cells. Though TPA-induced translocation of PKC isoforms was identical in both cell lines, down regulation of PKCδ was defective in resistant cells. Therefore, a deregulation in PKCδ was associated with cisplatin resistance. | |
dc.format.mimetype | application/pdf | |
dc.identifier.uri | https://hdl.handle.net/20.500.12503/26092 | |
dc.language.iso | en | |
dc.provenance.legacyDownloads | 0 | |
dc.subject | Cancer Biology | |
dc.subject | Cell and Developmental Biology | |
dc.subject | Cell Biology | |
dc.subject | Cells | |
dc.subject | Cellular and Molecular Physiology | |
dc.subject | Life Sciences | |
dc.subject | Medical Cell Biology | |
dc.subject | Medicine and Health Sciences | |
dc.subject | Oncology | |
dc.subject | Other Cell and Developmental Biology | |
dc.subject | Other Pharmacy and Pharmaceutical Sciences | |
dc.subject | Pharmacology | |
dc.subject | Pharmacy and Pharmaceutical Sciences | |
dc.subject | Toxicology | |
dc.subject | Characterization | |
dc.subject | protein kinase C | |
dc.subject | cisplatin sensitive | |
dc.subject | cisplatin resistant | |
dc.subject | human cervical cancer | |
dc.subject | HeLa cells | |
dc.subject | signal transduction | |
dc.subject | carcinogenesis | |
dc.subject | cell death | |
dc.subject | cell proliferation | |
dc.subject | anticancer drugs | |
dc.subject | cytotoxicity | |
dc.subject | PKC | |
dc.title | Characterization of Protein Kinase C in Cisplatin Sensitive and Resistant Human Cervical Cancer HeLa Cells | |
dc.type | Thesis | |
dc.type.material | text | |
thesis.degree.department | Graduate School of Biomedical Sciences | |
thesis.degree.discipline | Microbiology and Immunology | |
thesis.degree.grantor | University of North Texas Health Science Center at Fort Worth | |
thesis.degree.name | Master of Science |
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