Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/107976
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dc.titleDifferential cellular zinc levels in metastatic and primary nasopharyngeal carcinoma
dc.contributor.authorBay, B.-H.
dc.contributor.authorChan, Y.-G.
dc.contributor.authorFong, C.-M.
dc.contributor.authorLeong, H.-K.
dc.date.accessioned2014-11-20T05:57:37Z
dc.date.available2014-11-20T05:57:37Z
dc.date.issued1997
dc.identifier.citationBay, B.-H.,Chan, Y.-G.,Fong, C.-M.,Leong, H.-K. (1997). Differential cellular zinc levels in metastatic and primary nasopharyngeal carcinoma. International Journal of Oncology 11 (4) : 745-748. ScholarBank@NUS Repository.
dc.identifier.issn10196439
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/107976
dc.description.abstractZinc levels are known to be elevated in certain cancer tissues. In this study, zinc content in metastatic and primary nasopharyngeal carcinoma (NPC) cells were quantitated by X-ray microanalysis at the ultrastructural level. Zinc levels of cancer cells derived from the cervical lymph node of a patient with metastatic carcinoma and that from the nasopharynx biopsy of another NPC patient with no clinical evidence of secondary spread, were analyzed. X-ray micro-analysis revealed significantly higher cellular zinc levels in metastatic NPC cells. Zinc is a known anti-apoptotic agent and tumor response to radiotherapy is linked with apoptosis or programmed cell death. Raised zinc levels observed here could provide the biological basis for the observation of a higher percentage of distant metastasis in cervical node positive NPC patients treated by radiotherapy (the mainstay of treatment for NPC) as compared to those without regional nodal disease.
dc.sourceScopus
dc.subjectCellular zinc content
dc.subjectMetastatic NPC
dc.subjectPrimary NPC
dc.subjectUltrastructure
dc.subjectX-ray microanalysis
dc.typeArticle
dc.contributor.departmentANATOMY
dc.description.sourcetitleInternational Journal of Oncology
dc.description.volume11
dc.description.issue4
dc.description.page745-748
dc.description.codenIJONE
dc.identifier.isiutNOT_IN_WOS
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