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Details

Autor(en) / Beteiligte
Titel
Colon cancer cells produce immunoregulatory glucocorticoids
Ist Teil von
  • Oncogene, 2011-05, Vol.30 (21), p.2411-2419
Ort / Verlag
London: Nature Publishing Group UK
Erscheinungsjahr
2011
Quelle
MEDLINE
Beschreibungen/Notizen
  • Glucocorticoids (GC) have important anti-inflammatory and pro-apoptotic activities. Initially thought to be exclusively produced by the adrenal glands, there is now increasing evidence for extra-adrenal sources of GCs. We have previously shown that the intestinal epithelium produces immunoregulatory GCs and that intestinal steroidogenesis is regulated by the nuclear receptor liver receptor homolog-1 (LRH-1). As LRH-1 has been implicated in the development of colon cancer, we here investigated whether LRH-1 regulates GC synthesis in colorectal tumors and whether tumor-produced GCs suppress T-cell activation. Colorectal cancer cell lines and primary tumors were found to express steroidogenic enzymes and regulatory factors required for the de novo synthesis of cortisol. Both cell lines and primary tumors constitutively produced readily detectable levels of cortisol, as measured by radioimmunoassay, thin-layer chromatography and bioassay. Whereas overexpression of LRH-1 significantly increased the expression of steroidogenic enzymes and the synthesis of cortisol, downregulation or inhibition of LRH-1 effectively suppressed these processes, indicating an important role of LRH-1 in colorectal tumor GC synthesis. An immunoregulatory role of tumor-derived GCs could be further confirmed by demonstrating a suppression of T-cell activation. This study describes for the first time cortisol synthesis in a non-endocrine tumor in humans, and suggests that the synthesis of bioactive GCs in colon cancer cells may account as a novel mechanism of tumor immune escape.
Sprache
Englisch
Identifikatoren
ISSN: 0950-9232
eISSN: 1476-5594
DOI: 10.1038/onc.2010.629
Titel-ID: cdi_proquest_miscellaneous_876244341
Format
Schlagworte
692/699/67/1504/1885/1393, Adrenal glands, Animals, Anti-Inflammatory Agents - metabolism, Anti-Inflammatory Agents - pharmacology, Apoptosis, Apoptosis - drug effects, Biological and medical sciences, Caco-2 Cells, Cancer cells, Cell activation, Cell Biology, Cell physiology, Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes, Cellular biology, Cholesterol Side-Chain Cleavage Enzyme - genetics, Chromatography, Thin Layer, Colon cancer, Colonic Neoplasms - genetics, Colonic Neoplasms - metabolism, Colonic Neoplasms - pathology, Colorectal cancer, Colorectal carcinoma, Corticosteroids, Cortisol, Culture Media, Conditioned - pharmacology, Development and progression, Enzymes, Epithelium, Fundamental and applied biological sciences. Psychology, Gastroenterology. Liver. Pancreas. Abdomen, Gene Expression Regulation, Neoplastic, Genetic aspects, Genomics, Glucocorticoids, Glucocorticoids - metabolism, Glucocorticoids - pharmacology, HEK293 Cells, Hormones, HT29 Cells, Human Genetics, Humans, Hydrocortisone, Hydrocortisone - metabolism, Hydrocortisone - pharmacology, Immunology, Immunoregulation, Inflammation, Internal Medicine, Intestine, Liver, Lymphocyte Activation - drug effects, Lymphocytes T, Medical sciences, Medicine, Medicine & Public Health, Mice, Mice, Inbred C57BL, Molecular and cellular biology, Nuclear receptors, Oncology, original-article, Phosphoproteins - genetics, Physiological aspects, Radioimmunoassay, Receptors, Cytoplasmic and Nuclear - genetics, Reverse Transcriptase Polymerase Chain Reaction, RNA Interference, Spleen - cytology, Steroid 11-beta-Hydroxylase - genetics, Steroidogenesis, Steroids, Stomach. Duodenum. Small intestine. Colon. Rectum. Anus, T-Lymphocytes - drug effects, T-Lymphocytes - metabolism, Thin-layer chromatography, Thymus Gland - cytology, Tumor cell lines, Tumors

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