{"id":1118530,"date":"2023-10-13T23:37:21","date_gmt":"2023-10-14T03:37:21","guid":{"rendered":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/uncategorized\/ovaprint-a-cell-free-dna-methylation-liquid-biopsy-for-the-risk-cancer-discovery\/"},"modified":"2023-10-13T23:37:21","modified_gmt":"2023-10-14T03:37:21","slug":"ovaprint-a-cell-free-dna-methylation-liquid-biopsy-for-the-risk-cancer-discovery","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/dna\/ovaprint-a-cell-free-dna-methylation-liquid-biopsy-for-the-risk-cancer-discovery\/","title":{"rendered":"OvaPrint  a cell-free DNA methylation liquid biopsy for the risk &#8230; &#8211; Cancer Discovery"},"content":{"rendered":"<p><p>      Purpose High-grade serous ovarian carcinoma (HGSOC) is the      most lethal epithelial ovarian cancer (EOC) and is often      diagnosed at late stage. In women with a known pelvic mass,      surgery followed by pathological assessment is the most      reliable way to diagnose EOC and there are still no effective      screening tools in asymptomatic women. In the current study      we developed a cfDNA methylation liquid biopsy for the risk      assessment of early-stage HGSOC. Experimental Design We      performed reduced representation bisulfite sequencing to      identify differentially methylated regions (DMRs) between      HGSOC and normal ovarian and fallopian tube tissue. Next, we      performed hybridization probe capture for 1677 DMRs and      constructed a classifier (OvaPrint) on an independent set of      cfDNA samples to discriminate HGSOC from benign masses. We      also analyzed a series of non-HGSOC EOC, including low-grade,      and borderline samples to assess the generalizability of      OvaPrint. A total of 372 samples (tissue n=59, plasma n=313)      were analyzed in this study. Results OvaPrint achieved a      positive predictive value of 95% and a negative predictive      value of 88% for discriminating HGSOC from benign masses,      surpassing other commercial tests. OvaPrint was less      sensitive for non-HGSOC EOC, albeit it may have potential      utility for identifying low-grade and borderline tumors with      higher malignant potential. Conclusions OvaPrint is a highly      sensitive and specific test that can be used for the risk      assessment of HGSOC in symptomatic women. Prospective studies      are warranted to validate OvaPrint for HGSOC and further      develop it for non-HGSOC EOC histotypes in both symptomatic      and asymptomatic women with adnexal masses.    <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read the original here:<br \/>\n<a target=\"_blank\" href=\"https:\/\/aacrjournals.org\/clincancerres\/article\/doi\/10.1158\/1078-0432.CCR-23-1197\/729529\/OvaPrintT-a-cell-free-DNA-methylation-liquid\" title=\"OvaPrint  a cell-free DNA methylation liquid biopsy for the risk ... - Cancer Discovery\" rel=\"noopener\">OvaPrint  a cell-free DNA methylation liquid biopsy for the risk ... - Cancer Discovery<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Purpose High-grade serous ovarian carcinoma (HGSOC) is the most lethal epithelial ovarian cancer (EOC) and is often diagnosed at late stage. In women with a known pelvic mass, surgery followed by pathological assessment is the most reliable way to diagnose EOC and there are still no effective screening tools in asymptomatic women <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/dna\/ovaprint-a-cell-free-dna-methylation-liquid-biopsy-for-the-risk-cancer-discovery\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[26],"tags":[],"class_list":["post-1118530","post","type-post","status-publish","format-standard","hentry","category-dna"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/1118530"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=1118530"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/1118530\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=1118530"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=1118530"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=1118530"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}