Trace elements in head and neck cancer patients: Zinc status and immunologic functions
In this study we have assessed zinc status and zinc-dependent cell-mediated immune functions (interleukin-2 production by mononuclear cells, natural killer cell lytic activity, and interleukin-1β production by mononuclear cells) in adult patients with squamous cell carcinoma of the upper aerodigesti...
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Veröffentlicht in: | Otolaryngology-head and neck surgery 1997-06, Vol.116 (6), p.624-629 |
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creator | PRASAD, ANANDA S. KAPLAN, JOSEPH BECK, FRANCES W.J. PENNY, HAYWARD S. SHAMSA, FALAH H. SALWEN, WALTER A. MARKS, STEVEN C. MATHOG, ROBERT H. |
description | In this study we have assessed zinc status and zinc-dependent cell-mediated immune functions (interleukin-2 production by mononuclear cells, natural killer cell lytic activity, and interleukin-1β production by mononuclear cells) in adult patients with squamous cell carcinoma of the upper aerodigestive tract at diagnosis and before any therapy was instituted. Inasmuch as significant interactions between zinc, copper, and iron exist, we also assayed the plasma copper level, serum iron level, and total iron-binding capacity in our patients. We recruited 30 cancer subjects and 21 control subjects. On the basis of cellular zinc criteria, we diagnosed a mild deficiency of zinc in 53% of cancer subjects. The plasma zinc level was not decreased in our subjects. A univariate analysis was applied by use of one-way analysis of variance comparing study variables among the three study groups (controls and zinc-deficient and zinc-sufficient cancer patients) and Tukey’s multiple comparison test, and we showed that interleukin-2 production and natural killer lytic activity were decreased in zinc-deficient cancer patients. Interleukin-1β production (ELISA assay) was increased in both zinc-deficient and zinc-sufficient groups. Plasma copper level was not different, but the iron utilization was decreased in both groups of cancer subjects. We conclude that zinc deficiency and zinc-dependent immunologic dysfunctions are present in more than half of the patients with head and neck cancer in the Detroit area. (Otolaryngol Head Neck Surg 1997;116:624-9.) |
doi_str_mv | 10.1016/S0194-5998(97)70238-9 |
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Prasad and Beck), Departments of Otolaryngology (Drs. Mathog and Marks), Pediatrics (Dr. Kaplan), and Radiation-Oncology (Dr. Shamsa), Wayne State University School of Medicine, Harper Hospital (H. Penny), and Veterans Administration Medical Center (Dr. Salwen)</creatorcontrib><description>In this study we have assessed zinc status and zinc-dependent cell-mediated immune functions (interleukin-2 production by mononuclear cells, natural killer cell lytic activity, and interleukin-1β production by mononuclear cells) in adult patients with squamous cell carcinoma of the upper aerodigestive tract at diagnosis and before any therapy was instituted. Inasmuch as significant interactions between zinc, copper, and iron exist, we also assayed the plasma copper level, serum iron level, and total iron-binding capacity in our patients. We recruited 30 cancer subjects and 21 control subjects. On the basis of cellular zinc criteria, we diagnosed a mild deficiency of zinc in 53% of cancer subjects. The plasma zinc level was not decreased in our subjects. A univariate analysis was applied by use of one-way analysis of variance comparing study variables among the three study groups (controls and zinc-deficient and zinc-sufficient cancer patients) and Tukey’s multiple comparison test, and we showed that interleukin-2 production and natural killer lytic activity were decreased in zinc-deficient cancer patients. Interleukin-1β production (ELISA assay) was increased in both zinc-deficient and zinc-sufficient groups. Plasma copper level was not different, but the iron utilization was decreased in both groups of cancer subjects. We conclude that zinc deficiency and zinc-dependent immunologic dysfunctions are present in more than half of the patients with head and neck cancer in the Detroit area. (Otolaryngol Head Neck Surg 1997;116:624-9.)</description><identifier>ISSN: 0194-5998</identifier><identifier>EISSN: 1097-6817</identifier><identifier>DOI: 10.1016/S0194-5998(97)70238-9</identifier><identifier>PMID: 29389280</identifier><language>eng</language><publisher>Sage CA: Los Angeles, CA: Mosby, Inc</publisher><ispartof>Otolaryngology-head and neck surgery, 1997-06, Vol.116 (6), p.624-629</ispartof><rights>1997 Mosby, Inc.</rights><rights>1997 American Association of Otolaryngology‐Head and Neck Surgery Foundation (AAO‐HNSF)</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4489-e432d011c7c02f87e2c9e53d84c0f56eafa1cff138693e3c81184598290d4dc93</citedby><cites>FETCH-LOGICAL-c4489-e432d011c7c02f87e2c9e53d84c0f56eafa1cff138693e3c81184598290d4dc93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1016%2FS0194-5998%2897%2970238-9$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1016%2FS0194-5998%2897%2970238-9$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29389280$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PRASAD, ANANDA S.</creatorcontrib><creatorcontrib>KAPLAN, JOSEPH</creatorcontrib><creatorcontrib>BECK, FRANCES W.J.</creatorcontrib><creatorcontrib>PENNY, HAYWARD S.</creatorcontrib><creatorcontrib>SHAMSA, FALAH H.</creatorcontrib><creatorcontrib>SALWEN, WALTER A.</creatorcontrib><creatorcontrib>MARKS, STEVEN C.</creatorcontrib><creatorcontrib>MATHOG, ROBERT H.</creatorcontrib><creatorcontrib>From the Division of Hematology-Oncology, Department of Internal Medicine (Drs. Prasad and Beck), Departments of Otolaryngology (Drs. Mathog and Marks), Pediatrics (Dr. Kaplan), and Radiation-Oncology (Dr. Shamsa), Wayne State University School of Medicine, Harper Hospital (H. Penny), and Veterans Administration Medical Center (Dr. Salwen)</creatorcontrib><title>Trace elements in head and neck cancer patients: Zinc status and immunologic functions</title><title>Otolaryngology-head and neck surgery</title><addtitle>Otolaryngol Head Neck Surg</addtitle><description>In this study we have assessed zinc status and zinc-dependent cell-mediated immune functions (interleukin-2 production by mononuclear cells, natural killer cell lytic activity, and interleukin-1β production by mononuclear cells) in adult patients with squamous cell carcinoma of the upper aerodigestive tract at diagnosis and before any therapy was instituted. Inasmuch as significant interactions between zinc, copper, and iron exist, we also assayed the plasma copper level, serum iron level, and total iron-binding capacity in our patients. We recruited 30 cancer subjects and 21 control subjects. On the basis of cellular zinc criteria, we diagnosed a mild deficiency of zinc in 53% of cancer subjects. The plasma zinc level was not decreased in our subjects. A univariate analysis was applied by use of one-way analysis of variance comparing study variables among the three study groups (controls and zinc-deficient and zinc-sufficient cancer patients) and Tukey’s multiple comparison test, and we showed that interleukin-2 production and natural killer lytic activity were decreased in zinc-deficient cancer patients. Interleukin-1β production (ELISA assay) was increased in both zinc-deficient and zinc-sufficient groups. Plasma copper level was not different, but the iron utilization was decreased in both groups of cancer subjects. We conclude that zinc deficiency and zinc-dependent immunologic dysfunctions are present in more than half of the patients with head and neck cancer in the Detroit area. 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Prasad and Beck), Departments of Otolaryngology (Drs. Mathog and Marks), Pediatrics (Dr. Kaplan), and Radiation-Oncology (Dr. Shamsa), Wayne State University School of Medicine, Harper Hospital (H. Penny), and Veterans Administration Medical Center (Dr. Salwen)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Otolaryngology-head and neck surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PRASAD, ANANDA S.</au><au>KAPLAN, JOSEPH</au><au>BECK, FRANCES W.J.</au><au>PENNY, HAYWARD S.</au><au>SHAMSA, FALAH H.</au><au>SALWEN, WALTER A.</au><au>MARKS, STEVEN C.</au><au>MATHOG, ROBERT H.</au><aucorp>From the Division of Hematology-Oncology, Department of Internal Medicine (Drs. Prasad and Beck), Departments of Otolaryngology (Drs. 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Inasmuch as significant interactions between zinc, copper, and iron exist, we also assayed the plasma copper level, serum iron level, and total iron-binding capacity in our patients. We recruited 30 cancer subjects and 21 control subjects. On the basis of cellular zinc criteria, we diagnosed a mild deficiency of zinc in 53% of cancer subjects. The plasma zinc level was not decreased in our subjects. A univariate analysis was applied by use of one-way analysis of variance comparing study variables among the three study groups (controls and zinc-deficient and zinc-sufficient cancer patients) and Tukey’s multiple comparison test, and we showed that interleukin-2 production and natural killer lytic activity were decreased in zinc-deficient cancer patients. Interleukin-1β production (ELISA assay) was increased in both zinc-deficient and zinc-sufficient groups. Plasma copper level was not different, but the iron utilization was decreased in both groups of cancer subjects. 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title | Trace elements in head and neck cancer patients: Zinc status and immunologic functions |
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