{"id":1023,"date":"2020-08-26T09:32:39","date_gmt":"2020-08-26T09:32:39","guid":{"rendered":"https:\/\/clinlabint.3wstaging.nl\/potential-genetic-cause-of-cushing-syndrome-found\/"},"modified":"2021-01-08T11:09:18","modified_gmt":"2021-01-08T11:09:18","slug":"potential-genetic-cause-of-cushing-syndrome-found","status":"publish","type":"post","link":"https:\/\/clinlabint.com\/potential-genetic-cause-of-cushing-syndrome-found\/","title":{"rendered":"Potential genetic cause of Cushing syndrome found"},"content":{"rendered":"<p><span lang=\"EN-GB\">A small study by researchers at the National Institutes of Health suggests that mutations in the gene CABLES1 may lead to Cushing syndrome, a rare disorder in which the body overproduces the stress hormone cortisol. &nbsp;<\/span><br \/>\n<span lang=\"EN-GB\">The excess cortisol found in Cushing syndrome can result from certain steroid medications or from tumours of the pituitary or adrenal glands. Symptoms of the disease include obesity, muscle weakness, fatigue, high blood pressure, high blood sugar, depression and anxiety.<\/span><br \/>\n<span lang=\"EN-GB\">Researchers at NIH\u2019s Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), in collaboration with researchers at other institutions in the United States, France and Canada, scanned tumour and cell tissue from 146 children with pituitary tumours evaluated for Cushing syndrome at the NIH Clinical Center. Researchers also scanned the genes of tumours from some of the children. Investigators in France scanned the genes of an additional 35 adult patients with Cushing syndrome and pituitary tumours.<\/span><br \/>\n<span lang=\"EN-GB\">The research team found that four of the patients have mutant forms of CABLES1 that do not respond to cortisol. This is significant because, when functioning normally, the CABLES1 protein, expressed by the CABLES1 gene, slows the division and growth of pituitary cells that produce the hormone adrenocorticotropin (ACTH). In turn, ACTH stimulates the adrenal gland to produce cortisol, which then acts on the pituitary gland to halt the growth of ACTH-producing cells, effectively suppressing any tumour development. Because cortisol does not affect the four mutant forms of CABLES1 discovered by the researchers, these genes leave production of ACTH-releasing cells unchecked.<\/span><br \/>\n<span lang=\"EN-GB\">\u201cThe mutations we identified impair the tumour suppressor function in the pituitary gland,\u201d said the study\u2019s senior author Constantine A. Stratakis, M.D., director of the NICHD Division of Intramural Research. \u201cThis discovery could lead to the development of treatment strategies that simulate the function of the CABLES1 protein and prevent recurrence of pituitary tumors in people with Cushing syndrome.\u201d<\/p>\n<p><\/span><br \/>\n<span lang=\"EN-GB\">Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)<\/span><br \/>\n<span lang=\"EN-GB\"><link https:\/\/www.nichd.nih.gov\/news\/releases\/Pages\/060117-pituitary-tumor.aspx _blank external-link-new-window \"Opens external link in new window\">www.nichd.nih.gov\/news\/releases\/Pages\/060117-pituitary-tumor.aspx<\/link><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>A small study by researchers at the National Institutes of Health suggests that mutations in the gene CABLES1 may lead to Cushing syndrome, a rare disorder in which the body overproduces the stress hormone cortisol. &nbsp; The excess cortisol found in Cushing syndrome can result from certain steroid medications or from tumours of the pituitary [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[35],"tags":[],"_links":{"self":[{"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/posts\/1023"}],"collection":[{"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/comments?post=1023"}],"version-history":[{"count":0,"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/posts\/1023\/revisions"}],"wp:attachment":[{"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/media?parent=1023"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/categories?post=1023"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/clinlabint.com\/wp-json\/wp\/v2\/tags?post=1023"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}