Differential cellular zinc levels in metastatic and primary nasopharyngeal carcinoma

  • Authors:
    • B Bay
    • Y Chan
    • C Fong
    • H Leong
  • View Affiliations

  • Published online on: October 1, 1997     https://doi.org/10.3892/ijo.11.4.745
  • Pages: 745-748
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Abstract

Zinc 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 microanalysis 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.

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October 1997
Volume 11 Issue 4

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
Bay B, Chan Y, Fong C and Leong H: Differential cellular zinc levels in metastatic and primary nasopharyngeal carcinoma. Int J Oncol 11: 745-748, 1997
APA
Bay, B., Chan, Y., Fong, C., & Leong, H. (1997). Differential cellular zinc levels in metastatic and primary nasopharyngeal carcinoma. International Journal of Oncology, 11, 745-748. https://doi.org/10.3892/ijo.11.4.745
MLA
Bay, B., Chan, Y., Fong, C., Leong, H."Differential cellular zinc levels in metastatic and primary nasopharyngeal carcinoma". International Journal of Oncology 11.4 (1997): 745-748.
Chicago
Bay, B., Chan, Y., Fong, C., Leong, H."Differential cellular zinc levels in metastatic and primary nasopharyngeal carcinoma". International Journal of Oncology 11, no. 4 (1997): 745-748. https://doi.org/10.3892/ijo.11.4.745