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      TNFa increases in vitro migration of human HPV18-positive SW756 cervical carcinoma cells

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          Abstract

          TNFa has been associated with both, tumor survival and apoptosis. This cytokine is also involved in promoting cell migration during wound healing and tumorigenesis. SW756 is a HPV18-positive cervical carcinoma cell line, which has been used to study different mechanisms of cervical cancer progression. An in vitro assay of scratch wound healing onto monolayers of SW756 cells was used to assess the effect of TNFa on cell migration into a wound space. It was found that SW756 cells have the ability to migrate, but not proliferate in response to scratch wounding in a serum-free medium supplemented with TNFa. RT-PCR analysis showed that SW756 cells express TNFa mRNA when incubated in medium with and without serum. Wound closure and migration rate of SW756 cells were significantly increased in the presence of serum-free media supplemented with TNFa (10 ng/mL) as compared to serum-free media, and media supplemented with either anti-TNFa antibody or both TNFa and anti-TNFa antibody (p<0.05). The results showed a stimulatory effect of TNFa on the migration of SW756 cervical carcinoma cells, suggesting a novel and important role for TNFa in cervical cancer progression.

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          Most cited references72

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          Cell migration: a physically integrated molecular process.

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            The TNF and TNF receptor superfamilies: integrating mammalian biology.

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              JNK phosphorylates paxillin and regulates cell migration.

              The c-Jun amino-terminal kinase (JNK) is generally thought to be involved in inflammation, proliferation and apoptosis. Accordingly, its substrates are transcription factors and anti-apoptotic proteins. However, JNK has also been shown to be required for Drosophila dorsal closure, and MAP kinase/ERK kinase kinase 1, an upstream kinase in the JNK pathway, has been shown to be essential for cell migration. Both results imply that JNK is important in cell migration. Here we show that JNK1 is required for the rapid movement of both fish keratocytes and rat bladder tumour epithelial cells (NBT-II). Moreover, JNK1 phosphorylates serine 178 on paxillin, a focal adhesion adaptor, both in vitro and in intact cells. NBT-II cells expressing the Ser 178 --> Ala mutant of paxillin (Pax(S178A)) formed focal adhesions and exhibited the limited movement associated with such contacts in both single-cell-migration and wound-healing assays. In contrast, cells expressing wild-type paxillin moved rapidly and retained close contacts as the predominant adhesion. Expression of Pax(S178A) also inhibited the migration of two other cell lines. Thus, phosphorylation of paxillin by JNK seems essential for maintaining the labile adhesions required for rapid cell migration.
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                Author and article information

                Journal
                biocell
                Biocell
                Biocell
                Sociedad Latinoamericana de Microscopía Electrónica.; Centro Regional de Investigaciones Científicas y Tecnológicas (Mendoza, Argentina) (Mendoza, Mendoza, Argentina )
                0327-9545
                1667-5746
                December 2005
                : 29
                : 3
                : 303-311
                Affiliations
                [01] orgnameUniversidad de Concepción orgdiv1Faculty of Biological Sciences
                [02] orgnameUniversidad de Concepción orgdiv1College of Dentistry
                [03] orgnameUniversidad Nacional de Cuyo orgdiv1Faculty of Medical Sciences
                Article
                S0327-95452005000300008 S0327-9545(05)02900300008
                3aa27e03-9533-4c89-a2e2-f6b122a77952

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

                History
                : 25 February 2005
                : 27 May 2005
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 43, Pages: 9
                Product

                SciELO Argentina


                SW756,TNFa,Migration,Carcinoma,Wound healing assay
                SW756, TNFa, Migration, Carcinoma, Wound healing assay

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