{"id":74865,"date":"2024-06-17T14:14:25","date_gmt":"2024-06-17T14:14:25","guid":{"rendered":"https:\/\/news.talkwithrattan.com\/index.php\/2024\/06\/17\/breakthrough-means-painful-giant-moles-that-develop-in-rare-condition-cmn-could-be-reversed\/"},"modified":"2024-06-17T14:14:25","modified_gmt":"2024-06-17T14:14:25","slug":"breakthrough-means-painful-giant-moles-that-develop-in-rare-condition-cmn-could-be-reversed","status":"publish","type":"post","link":"https:\/\/news.talkwithrattan.com\/index.php\/2024\/06\/17\/breakthrough-means-painful-giant-moles-that-develop-in-rare-condition-cmn-could-be-reversed\/","title":{"rendered":"Breakthrough means painful, giant moles that develop in rare condition CMN could be reversed"},"content":{"rendered":"<div style=\"text-align:center\"><img loading=\"lazy\" decoding=\"async\" width=\"563\" height=\"750\" src=\"https:\/\/i1.wp.com\/e3.365dm.com\/24\/06\/563x750\/skynews-cmn-caring-matters-now_6583885.jpg?20240617131820&amp;fit=563,750&amp;ssl=1\" class=\"attachment-post-thumbnail size-post-thumbnail wp-post-image\" alt=\"Breakthrough means painful, giant moles that develop in rare condition CMN could be reversed\" title=\"Breakthrough means painful, giant moles that develop in rare condition CMN could be reversed\" \/><\/div><p> <br \/>\n<\/p>\n<div data-component-name=\"sdc-article-body\" data-highlight-intro=\"true\">\n<p>A new genetic therapy has been developed that could reverse giant, debilitating moles that accompany a rare skin condition.<\/p>\n<p>Congenital melanocytic naevus syndrome, or CMN for short, sees children born with up to 80% of their body covered in big, painful or itchy moles.<\/p>\n<p>They are caused by genetic mutations acquired in the womb &#8211; and in some cases, these moles can develop into melanoma.<\/p>\n<div class=\"sdc-article-widget sdc-article-image\">\n<figure class=\"sdc-article-image__figure\">\n<div class=\"sdc-article-image__wrapper\" data-aspect-ratio=\"3\/4\"><\/div><figcaption class=\"ui-media-caption\">\n        <span class=\"u-hide-visually\">Image:<\/span><br \/>\n        <span class=\"ui-media-caption__caption-text\">Pic: @mrelbank and @caringmattersnow<br \/>\n        <\/span><br \/>\n      <\/figcaption><\/figure>\n<\/div>\n<p>During trials in mice with CMNS, researchers silenced a gene called NRAS, which triggered the mole cells to self-destruct.<\/p>\n<p>The treatment could one day be used to reverse the giant moles seen in CMN patients, and potentially more common types of moles.<\/p>\n<p>Veronica Kinsler, who led the research, said: &#8220;CMN is physically and mentally challenging for children and adults living with this condition and for their families.<\/p>\n<p>&#8220;These results are very exciting, as not only does the genetic therapy trigger self-destruction of the mole cells in the lab, but we have managed to deliver it into the skin in mice.&#8221;<\/p>\n<p>She cautioned that more testing is required before the therapy can be given to patients &#8211; but it is hoped clinical trials involving people will begin soon.<\/p>\n<div class=\"sdc-article-widget sdc-article-image\">\n<figure class=\"sdc-article-image__figure\">\n<div class=\"sdc-article-image__wrapper\" data-aspect-ratio=\"16\/9\">\n          <img decoding=\"async\" class=\"sdc-article-image__item\" loading=\"lazy\" intrinsicsize=\"768x432\" src=\"https:\/\/e3.365dm.com\/24\/06\/768x432\/skynews-cmn-study_6583891.jpg?20240617131959\" srcset=\"https:\/\/e3.365dm.com\/24\/06\/384x216\/skynews-cmn-study_6583891.jpg?20240617131959 380w, https:\/\/e3.365dm.com\/24\/06\/768x432\/skynews-cmn-study_6583891.jpg?20240617131959 760w, https:\/\/e3.365dm.com\/24\/06\/1600x900\/skynews-cmn-study_6583891.jpg?20240617131959 1024w, https:\/\/e3.365dm.com\/24\/06\/2048x1152\/skynews-cmn-study_6583891.jpg?20240617131959 2048w\" sizes=\"(min-width: 1024px) 1024px, 100vw\" alt=\" \"\/>\n    <\/div>\n<\/figure>\n<\/div>\n<p>The study was carried out by researchers from the Francis Crick Institute, UCL Great Ormond Street Institute for Child Health, and Great Ormond Street Hospital for Children.<\/p>\n<p>It was partly funded by Caring Matters Now, a charity devoted to supporting people with CMN &#8211; and its CEO has described the results as a breakthrough that could transform lives.<\/p>\n<p>Jodi Whitehouse said: &#8220;Speaking as someone who was born with CMN covering 70% of my body and having undergone more than 30 operations in my childhood to try and remove the CMN because of the fear of melanoma, with no success, this news is awe inspiring and exciting. It brings real hope to the lives of those living with CMN.&#8221;<\/p>\n<p><strong>Read more from Sky News:<br \/><a href=\"https:\/\/news.sky.com\/story\/sir-rod-stewart-booed-by-german-crowd-while-making-show-of-support-for-ukraine-13154166\" target=\"_blank\" rel=\"noopener\">Rod Stewart &#8216;booed&#8217; by German crowd<\/a><br \/><a href=\"https:\/\/news.sky.com\/story\/e-coli-outbreak-public-warned-not-to-eat-specific-product-recalled-as-precautionary-measure-13154193\" target=\"_blank\" rel=\"noopener\">New product recalled over E.coli fears<\/a><br \/><a href=\"https:\/\/news.sky.com\/story\/alan-hansen-former-teammate-graeme-souness-gives-positive-update-on-liverpool-legend-13154328\" target=\"_blank\" rel=\"noopener\">Update on Alan Hansen&#8217;s condition<\/a><\/strong><\/p>\n<div class=\"sdc-article-widget sdc-article-image\">\n<figure class=\"sdc-article-image__figure\">\n<div class=\"sdc-article-image__wrapper\" data-aspect-ratio=\"16\/9\">\n          <img decoding=\"async\" class=\"sdc-article-image__item\" loading=\"lazy\" intrinsicsize=\"768x432\" src=\"https:\/\/e3.365dm.com\/24\/06\/768x432\/skynews-hanna-cmn_6583893.jpg?20240617132049\" srcset=\"https:\/\/e3.365dm.com\/24\/06\/384x216\/skynews-hanna-cmn_6583893.jpg?20240617132049 380w, https:\/\/e3.365dm.com\/24\/06\/768x432\/skynews-hanna-cmn_6583893.jpg?20240617132049 760w, https:\/\/e3.365dm.com\/24\/06\/1600x900\/skynews-hanna-cmn_6583893.jpg?20240617132049 1024w, https:\/\/e3.365dm.com\/24\/06\/2048x1152\/skynews-hanna-cmn_6583893.jpg?20240617132049 2048w\" sizes=\"(min-width: 1024px) 1024px, 100vw\" alt=\"Hanna's CMN makes her everyday life challenging\"\/>\n    <\/div><figcaption class=\"ui-media-caption\">\n        <span class=\"u-hide-visually\">Image:<\/span><br \/>\n        <span class=\"ui-media-caption__caption-text\">Hanna&#8217;s CMN makes her everyday life challenging<br \/>\n        <\/span><br \/>\n      <\/figcaption><\/figure>\n<\/div>\n<p><strong>Hope for families<\/strong><\/p>\n<p>Skin cells from children born with CMN were used in the study after being donated by their parents.<\/p>\n<p>One of them is Hanna, a seven-year-old born with a dark lesion covering her back, stomach and thighs.<\/p>\n<p>It leaves her skin itchy and dry, with large lumpy nodules that make sleeping at night difficult and everyday life challenging.<\/p>\n<div class=\"sdc-article-widget sdc-article-image\">\n<figure class=\"sdc-article-image__figure\">\n<div class=\"sdc-article-image__wrapper\" data-aspect-ratio=\"16\/9\">\n          <img decoding=\"async\" class=\"sdc-article-image__item\" loading=\"lazy\" intrinsicsize=\"768x432\" src=\"https:\/\/e3.365dm.com\/24\/06\/768x432\/skynews-cmn-ada_6583892.jpg?20240617132018\" srcset=\"https:\/\/e3.365dm.com\/24\/06\/384x216\/skynews-cmn-ada_6583892.jpg?20240617132018 380w, https:\/\/e3.365dm.com\/24\/06\/768x432\/skynews-cmn-ada_6583892.jpg?20240617132018 760w, https:\/\/e3.365dm.com\/24\/06\/1600x900\/skynews-cmn-ada_6583892.jpg?20240617132018 1024w, https:\/\/e3.365dm.com\/24\/06\/2048x1152\/skynews-cmn-ada_6583892.jpg?20240617132018 2048w\" sizes=\"(min-width: 1024px) 1024px, 100vw\" alt=\"Ada's skin cells were donated to the study\"\/>\n    <\/div><figcaption class=\"ui-media-caption\">\n        <span class=\"u-hide-visually\">Image:<\/span><br \/>\n        <span class=\"ui-media-caption__caption-text\">Ada&#8217;s skin cells were donated to the study<br \/>\n        <\/span><br \/>\n      <\/figcaption><\/figure>\n<\/div>\n<p>Ada, who is three years old, has 70% of her body covered in CMN &#8211; mostly on her neck and back.<\/p>\n<p>She loves swimming and the sea, but needs to take extra precautions including additional sun protection and good clothing.<\/p>\n<p>     <a href=\"https:\/\/news.sky.com\/download-app\" target=\"blank\" data-tracking-label=\"ui-app-promo-download-link\" class=\"ui-app-promo sdc-article-widget\" data-type=\"\" data-component-name=\"ui-app-promo\" rel=\"noopener\"><\/p>\n<p>    <\/a><\/p>\n<p>Her CMN is also itchy and painful, and she has previously undergone surgery to remove concerning nodules.<\/p>\n<p>Rachelle and Greg, Ada&#8217;s parents, said: &#8220;Knowing there has been a huge step forward in the CMN research and there could be a chance of Ada&#8217;s CMN being reversed and possibly reducing Ada&#8217;s risk of developing melanoma, has blown our expectations out the water.&#8221;<\/p>\n<\/p><\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/news.sky.com\/story\/breakthrough-means-painful-giant-moles-that-develop-in-rare-condition-cmn-could-be-reversed-13154389\">Source link <\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>A new genetic therapy has been developed that could reverse giant, debilitating moles that accompany a rare skin condition. Congenital melanocytic naevus syndrome, or CMN for short, sees children born with up to 80% of their body covered in big, painful or itchy moles. They are caused by genetic mutations acquired in the womb &#8211; [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":74866,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"tdm_status":"","tdm_grid_status":"","fifu_image_url":"https:\/\/e3.365dm.com\/24\/06\/563x750\/skynews-cmn-caring-matters-now_6583885.jpg?20240617131820","fifu_image_alt":"","footnotes":""},"categories":[607],"tags":[3588,68251,11119,3839,596,19138,68226,5030,9322,68227],"amp_enabled":true,"_links":{"self":[{"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/posts\/74865"}],"collection":[{"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/comments?post=74865"}],"version-history":[{"count":1,"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/posts\/74865\/revisions"}],"predecessor-version":[{"id":74867,"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/posts\/74865\/revisions\/74867"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/media\/74866"}],"wp:attachment":[{"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/media?parent=74865"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/categories?post=74865"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/news.talkwithrattan.com\/index.php\/wp-json\/wp\/v2\/tags?post=74865"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}