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Novel innate cancer killing activity in humans

BACKGROUND: In this study, we pilot tested an in vitro assay of cancer killing activity (CKA) in circulating leukocytes of 22 cancer cases and 25 healthy controls. METHODS: Using a human cervical cancer cell line, HeLa, as target cells, we compared the CKA in circulating leukocytes, as effector cell...

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Autores principales: Blanks, Michael J, Stehle, John R, Du, Wei, Adams, Jonathan M, Willingham, Mark C, Allen, Glenn O, Hu, Jennifer J, Lovato, James, Molnar, Istvan, Cui, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170245/
https://www.ncbi.nlm.nih.gov/pubmed/21813015
http://dx.doi.org/10.1186/1475-2867-11-26
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author Blanks, Michael J
Stehle, John R
Du, Wei
Adams, Jonathan M
Willingham, Mark C
Allen, Glenn O
Hu, Jennifer J
Lovato, James
Molnar, Istvan
Cui, Zheng
author_facet Blanks, Michael J
Stehle, John R
Du, Wei
Adams, Jonathan M
Willingham, Mark C
Allen, Glenn O
Hu, Jennifer J
Lovato, James
Molnar, Istvan
Cui, Zheng
author_sort Blanks, Michael J
collection PubMed
description BACKGROUND: In this study, we pilot tested an in vitro assay of cancer killing activity (CKA) in circulating leukocytes of 22 cancer cases and 25 healthy controls. METHODS: Using a human cervical cancer cell line, HeLa, as target cells, we compared the CKA in circulating leukocytes, as effector cells, of cancer cases and controls. The CKA was normalized as percentages of total target cells during selected periods of incubation time and at selected effector/target cell ratios in comparison to no-effector-cell controls. RESULTS: Our results showed that CKA similar to that of our previous study of SR/CR mice was present in human circulating leukocytes but at profoundly different levels in individuals. Overall, males have a significantly higher CKA than females. The CKA levels in cancer cases were lower than that in healthy controls (mean ± SD: 36.97 ± 21.39 vs. 46.28 ± 27.22). Below-median CKA was significantly associated with case status (odds ratio = 4.36; 95% Confidence Interval = 1.06, 17.88) after adjustment of gender and race. CONCLUSIONS: In freshly isolated human leukocytes, we were able to detect an apparent CKA in a similar manner to that of cancer-resistant SR/CR mice. The finding of CKA at lower levels in cancer patients suggests the possibility that it may be of a consequence of genetic, physiological, or pathological conditions, pending future studies with larger sample size.
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spelling pubmed-31702452011-09-10 Novel innate cancer killing activity in humans Blanks, Michael J Stehle, John R Du, Wei Adams, Jonathan M Willingham, Mark C Allen, Glenn O Hu, Jennifer J Lovato, James Molnar, Istvan Cui, Zheng Cancer Cell Int Primary Research BACKGROUND: In this study, we pilot tested an in vitro assay of cancer killing activity (CKA) in circulating leukocytes of 22 cancer cases and 25 healthy controls. METHODS: Using a human cervical cancer cell line, HeLa, as target cells, we compared the CKA in circulating leukocytes, as effector cells, of cancer cases and controls. The CKA was normalized as percentages of total target cells during selected periods of incubation time and at selected effector/target cell ratios in comparison to no-effector-cell controls. RESULTS: Our results showed that CKA similar to that of our previous study of SR/CR mice was present in human circulating leukocytes but at profoundly different levels in individuals. Overall, males have a significantly higher CKA than females. The CKA levels in cancer cases were lower than that in healthy controls (mean ± SD: 36.97 ± 21.39 vs. 46.28 ± 27.22). Below-median CKA was significantly associated with case status (odds ratio = 4.36; 95% Confidence Interval = 1.06, 17.88) after adjustment of gender and race. CONCLUSIONS: In freshly isolated human leukocytes, we were able to detect an apparent CKA in a similar manner to that of cancer-resistant SR/CR mice. The finding of CKA at lower levels in cancer patients suggests the possibility that it may be of a consequence of genetic, physiological, or pathological conditions, pending future studies with larger sample size. BioMed Central 2011-08-03 /pmc/articles/PMC3170245/ /pubmed/21813015 http://dx.doi.org/10.1186/1475-2867-11-26 Text en Copyright ©2011 Blanks et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Primary Research
Blanks, Michael J
Stehle, John R
Du, Wei
Adams, Jonathan M
Willingham, Mark C
Allen, Glenn O
Hu, Jennifer J
Lovato, James
Molnar, Istvan
Cui, Zheng
Novel innate cancer killing activity in humans
title Novel innate cancer killing activity in humans
title_full Novel innate cancer killing activity in humans
title_fullStr Novel innate cancer killing activity in humans
title_full_unstemmed Novel innate cancer killing activity in humans
title_short Novel innate cancer killing activity in humans
title_sort novel innate cancer killing activity in humans
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170245/
https://www.ncbi.nlm.nih.gov/pubmed/21813015
http://dx.doi.org/10.1186/1475-2867-11-26
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