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Altered phenotype in peripheral blood and tumor-associated NK cells from colorectal cancer patients

Title: Altered phenotype in peripheral blood and tumor-associated NK cells from colorectal cancer patients
Authors: Rocca, Yamila S; Roberti, María P; Arriaga, Juan M; Amat, Mora; Bruno, Luisina; Pampena, María B; Huertas, Eduardo; Loria, Fernando Sánchez; Pairola, Alejandro; Bianchini, Michele; Mordoh, José; Levy, Estrella M
Source: Innate Immunity ; volume 19, issue 1, page 76-85 ; ISSN 1753-4259 1753-4267
Publisher Information: SAGE Publications
Publication Year: 2012
Description: Despite NK cells being originally identified because of their ability to kill tumor cells in vitro, only limited information is available on NK cells infiltration of malignant tumors, especially in humans. NK cells infiltrating human colorectal carcinomas (CRCs) were analyzed to identify their potential protective role in an antitumor immune response. The expression and function of relevant molecules were analyzed from different sources, comparing tumor-associated NK cells (TANKs) with autologous peripheral blood NK cells (PB-NKs) from CRC patients—the latter in comparison with PB-NKs from normal donors. TANKs displayed a profound alteration of their phenotype with a drastic reduction of NK cell receptor expression. Co-culture experiments showed that CRC cells produce modulation in NK phenotype and functionality. Moreover, PB-NKs from CRC patients also exhibited an altered phenotype and profound defects in the ability to activate degranulation and IFN-γ production. For the first time, TANK and PB-NK cells from CRC patients have been characterized. It is shown that they are not capable of producing relevant cytokines and degranulate. Taken together, our results suggest that NK cells from CRC patients present alterations of phenotype and function therefore supporting the progression of cancer.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1177/1753425912453187
Availability: https://doi.org/10.1177/1753425912453187; https://journals.sagepub.com/doi/pdf/10.1177/1753425912453187; https://journals.sagepub.com/doi/full-xml/10.1177/1753425912453187
Rights: https://journals.sagepub.com/page/policies/text-and-data-mining-license
Accession Number: edsbas.9CFEE578
Database: BASE