Abstract
Expression of Transcribed Ultraconserved Regions (T-UCRs) is often deregulated in cancer. The present study assesses the expression and methylation of three T-UCRs (Uc160, Uc283 and Uc346) in colorectal cancer (CRC) and explores the potential of T-UCR methylation in circulating DNA for the detection of adenomas and adenocarcinomas.Expression levels of Uc160, Uc283 and Uc346 were lower in neoplastic tissues from 64 CRC patients (statistically significant for Uc160, p<0.001), compared to non-malignant tissues, while methylation levels displayed the inverse pattern (p<0.001, p=0.001 and p=0.004 respectively). In colon cancer cell lines, overexpression of Uc160 and Uc346 led to increased proliferation and migration rates. Methylation levels of Uc160 in plasma of 50 CRC, 59 adenoma patients, 40 healthy subjects and 12 patients with colon inflammation or diverticulosis predicted the presence of CRC with 35% sensitivity and 89% specificity (p=0.016), while methylation levels of the combination of all three T-UCRs resulted in 45% sensitivity and 74.3% specificity (p=0.013). In conclusion, studied T-UCRs’ expression and methylation status are deregulated in CRC while Uc160 and Uc346 appear to have a complicated role in CRC progression. Moreover their methylation status appears a promising non-invasive screening test for CRC, provided that the sensitivity of the assay is improved.
Highlights
Colorectal cancer (CRC) is the second leading cause of cancer-related deaths for men and third for women worldwide, with 50,260 cases estimated for 2017 in United States [1]
Methylation levels of Uc160 in plasma of 50 colorectal cancer (CRC), 59 adenoma patients, 40 healthy subjects and 12 patients with colon inflammation or diverticulosis predicted the presence of CRC with 35% sensitivity and 89% specificity (p=0.016), while methylation levels of the combination of all three T-Ultraconserved regions (UCRs) resulted in 45% sensitivity and 74.3% specificity (p=0.013)
Non-malignant tissues demonstrated higher expression levels of Uc160, Uc283 and Uc346 compared to adenocarcinomas, the difference was statistically significant only for Uc160 (p
Summary
Colorectal cancer (CRC) is the second leading cause of cancer-related deaths for men and third for women worldwide, with 50,260 cases estimated for 2017 in United States [1]. A long-term decline in CRC incidence rates has been noted since the mid-1980s, which has been attributed mostly to early screening through colonoscopy and removal of precancerous lesions [2, 3]. Screening for CRC through analysis of genetic or epigenetic markers in circulating cell-free DNA (ccfDNA), isolated from plasma or serum specimens, can provide a minimally invasive and low-cost method with higher probability of patient adherence compared to colonoscopy. An increasing number of studies have investigated the role of ccfDNA as a cancer biomarker, identifying tumour-derived genetic and epigenetic characteristics in serum/plasma samples [9,10,11,12,13,14,15,16,17,18]. For CRC, identification of DNA mutations or methylated genetic regions, offers a clinically useful biomarker for CRC screening and monitoring response to therapy [15, 19,20,21,22,23,24]
Sign-in/Register to view highlights & summary Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
