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Increased production of 27-hydroxycholesterol in human colorectal cancer advanced stage: Possible contribution to cancer cell survival and infiltration.
Rossin, D; Dias, I H K; Solej, M; Milic, I; Pitt, A R; Iaia, N; Scoppapietra, L; Devitt, A; Nano, M; Degiuli, M; Volante, M; Caccia, C; Leoni, V; Griffiths, H R; Spickett, C M; Poli, G; Biasi, F.
Affiliation
  • Rossin D; Dept. of Clinical and Biological Sciences, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: d.rossin@unito.it.
  • Dias IHK; Aston Research Centre for Healthy Ageing, School of Life and Health Sciences, Aston University, Birmingham, UK. Electronic address: h.k.i.dias1@aston.ac.uk.
  • Solej M; Dept. of Oncology, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: mario.solej@unito.it.
  • Milic I; Aston Research Centre for Healthy Ageing, School of Life and Health Sciences, Aston University, Birmingham, UK. Electronic address: i.milic@aston.ac.uk.
  • Pitt AR; Aston Research Centre for Healthy Ageing, School of Life and Health Sciences, Aston University, Birmingham, UK. Electronic address: a.r.pitt@aston.ac.uk.
  • Iaia N; Dept. of Clinical and Biological Sciences, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: noemi.iaia@unito.it.
  • Scoppapietra L; Dept. of Clinical and Biological Sciences, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: lara.scoppapietra@edu.unito.it.
  • Devitt A; Aston Research Centre for Healthy Ageing, School of Life and Health Sciences, Aston University, Birmingham, UK. Electronic address: a.devitt1@aston.ac.uk.
  • Nano M; Dept. of Clinical and Biological Sciences, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: marionano.md@gmail.com.
  • Degiuli M; Dept. of Oncology, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: maurizio.degiuli@unito.it.
  • Volante M; Dept. of Oncology, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: marco.volante@unito.it.
  • Caccia C; Genetics of Neurodegenerative and Metabolic Diseases, Dept. of Applied Diagnostic, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. Electronic address: claudio.caccia@istituto-besta.it.
  • Leoni V; Department of Laboratory Medicine, University of Milano-Bicocca, School of Medicine, Hospital of Desio, Desio, Milan, Italy. Electronic address: valerio.leoni@unimib.it.
  • Griffiths HR; Health and Medical Sciences, University of Surrey, Guildford, UK. Electronic address: h.r.griffiths@surrey.ac.uk.
  • Spickett CM; Aston Research Centre for Healthy Ageing, School of Life and Health Sciences, Aston University, Birmingham, UK. Electronic address: c.m.spickett@aston.ac.uk.
  • Poli G; Dept. of Clinical and Biological Sciences, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: giuseppe.poli@unito.it.
  • Biasi F; Dept. of Clinical and Biological Sciences, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy. Electronic address: fiorella.biasi@unito.it.
Free Radic Biol Med ; 136: 35-44, 2019 05 20.
Article in En | MEDLINE | ID: mdl-30910555
ABSTRACT
So far, the investigation in cancer cell lines of the modulation of cancer growth and progression by oxysterols, in particular 27-hydroxycholesterol (27HC), has yielded controversial results. The primary aim of this study was the quantitative evaluation of possible changes in 27HC levels during the different steps of colorectal cancer (CRC) progression in humans. A consistent increase in this oxysterol in CRC mass compared to the tumor-adjacent tissue was indeed observed, but only in advanced stages of progression (TNM stage III), a phase in which cancer has spread to nearby sites. To investigate possible pro-tumor properties of 27HC, its effects were studied in vitro in differentiated CaCo-2 cells. Relatively high concentrations of this oxysterol markedly increased the release of pro-inflammatory interleukins 6 and 8, monocyte chemoattractant protein-1, vascular endothelial growth factor, as well as matrix metalloproteinases 2 and 9. The up-regulation of all these molecules, which are potentially able to favor cancer progression, appeared to be dependent upon a net stimulation of Akt signaling exerted by supra-physiological amounts of 27HC.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Hydroxycholesterols Limits: Humans Language: En Journal: Free Radic Biol Med Journal subject: BIOQUIMICA / MEDICINA Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Hydroxycholesterols Limits: Humans Language: En Journal: Free Radic Biol Med Journal subject: BIOQUIMICA / MEDICINA Year: 2019 Document type: Article
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