Combined SEPT9 and BMP3 methylation in plasma for colorectal cancer early detection and screening in a Brazilian population

被引:9
|
作者
Lima, Adhara Brandao [1 ]
dos Reis, Mariana Bisarro [1 ]
Matsushita, Marcus [2 ]
dos Reis, Monise Tadin [2 ]
de Oliveira, Marco Antonio [3 ]
Reis, Rui Manuel [1 ,4 ,5 ]
Guimaraes, Denise Peixoto [1 ,6 ,7 ]
机构
[1] Barretos Canc Hosp, Mol Oncol Res Ctr, Barretos, Brazil
[2] Barretos Canc Hosp, Dept Pathol, Barretos, Brazil
[3] Barretos Canc Hosp, Nucleous Epidemiol & Stat, Barretos, Brazil
[4] Univ Minho, Life & Hlth Sci Res Inst ICVS, Med Sch, Braga, Portugal
[5] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
[6] Barretos Canc Hosp, Dept Endoscopy, Barretos, Brazil
[7] Barretos Canc Hosp, Mol Oncol Res Ctr, Rua Antenor Duarte Villela 1331, BR-14784400 Barretos, SP, Brazil
来源
CANCER MEDICINE | 2023年 / 12卷 / 15期
关键词
cell-free DNA; colorectal cancer; digital PCR; DNA methylation; liquid biopsy; MULTITARGET STOOL DNA; BIOMARKERS;
D O I
10.1002/cam4.6224
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Colorectal cancer (CRC) screening can help to reduce its incidence and mortality. Noninvasive strategies, such as plasma analysis of epigenetic alterations, can constitute important biomarkers of CRC detection.Objective: This study aimed to evaluate the plasma methylation status of SEPT9 and BMP3 promoters as biomarkers for detection of CRC and its precursor lesions in a Brazilian population.Methods: Plasma samples from 262 participants of the CRC screening program of Barretos Cancer Hospital who had a positive fecal occult blood test and underwent colonoscopy and cancer patients were analyzed. Participants were grouped according to the worst lesion detected in the colonoscopy. Cell-free circulating DNA (cfDNA) was bisulfite treated followed by the analysis of SEPT9 and BMP3 methylation status using a droplet digital PCR system (ddPCR). The best methylation cutoff value for group discrimination was calculated by receiver operating characteristic (ROC) curve analysis.Results: Among the 262 participants, 38 were diagnosed with CRC, 46 with advanced adenomas 119 with nonadvanced adenomas, three with sessile serrated lesions, and 13 with hyperplastic polyps. In 43 participants, no lesion was detected in the colonoscopy and were used as controls. The CRC group showed the highest cfDNA concentration (10.4 ng/mL). For the SEPT9 gene, a cutoff of 2.5% (AUC = 0.681) that discriminates between CRC and the control group resulted in CRC sensitivity and specificity of 50% and 90%, respectively. Concerning the BMP3 gene, a cutoff of 2.3% (AUC = 0.576) showed 40% and 90% of sensitivity and specificity for CRC detection, respectively. Combining SEPT9, BMP3 status, and age over 60 years resulted in a better performance for detecting CRC (AUC = 0.845) than the individual gene models, yielding 80% and 81% of sensitivity and specificity, respectively.Conclusion: The present study suggests that a combination of SEPT9 and BMP3 plasma methylation, along with age over 60 years, showed the highest performance in detecting CRC in a Brazilian population. These noninvasive biomarkers can potentially serve as useful tools for CRC screening programs.
引用
收藏
页码:15854 / 15867
页数:14
相关论文
共 50 条
  • [1] Advance in plasma SEPT9 gene methylation assay for colorectal cancer early detection
    Wang, Yu
    Chen, Pei-Min
    Liu, Rong-Bin
    WORLD JOURNAL OF GASTROINTESTINAL ONCOLOGY, 2018, 10 (01) : 15 - 22
  • [2] Advance in plasma SEPT9 gene methylation assay for colorectal cancer early detection
    Yu Wang
    Pei-Min Chen
    Rong-Bin Liu
    World Journal of Gastrointestinal Oncology, 2018, 10 (01) : 15 - 22
  • [3] Detection of Colorectal Cancer Using a Simplified SEPT9 Gene Methylation Assay Is a Reliable Method for Opportunistic Screening
    Wu, Dong
    Zhou, Guangpeng
    Jin, Peng
    Zhu, Jiqing
    Li, Shijie
    Wu, Qi
    Wang, Guiqi
    Sheng, Jianqiu
    Wang, Jianming
    Song, Lele
    Han, Xiaoliang
    Qian, Jiaming
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2016, 18 (04): : 535 - 545
  • [4] Detection of colorectal cancer by DNA methylation biomarker SEPT9: past, present and future
    Li, Yuemin
    Song, Lele
    Gong, Yuan
    He, Baoming
    BIOMARKERS IN MEDICINE, 2014, 8 (05) : 755 - 769
  • [5] Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer
    Church, Timothy Robert
    Wandell, Michael
    Lofton-Day, Catherine
    Mongin, Steven J.
    Burger, Matthias
    Payne, Shannon R.
    Castanos-Velez, Esmeralda
    Blumenstein, Brent A.
    Roesch, Thomas
    Osborn, Neal
    Snover, Dale
    Day, Robert W.
    Ransohoff, David F.
    GUT, 2014, 63 (02) : 317 - 325
  • [6] High methylation of the SEPT9 gene in Chinese colorectal cancer patients
    Su, X. L.
    Wang, Y. F.
    Li, S. J.
    Zhang, F.
    Cui, H. W.
    GENETICS AND MOLECULAR RESEARCH, 2014, 13 (02): : 2513 - 2520
  • [7] The SEPT9 gene methylation assay is capable of detecting colorectal adenoma in opportunistic screening
    Song, Lele
    Peng, Xiumei
    Li, Yuemin
    Xiao, Wenhua
    Jia, Jia
    Dong, Cheng
    Gong, Yuan
    Zhou, Guangpeng
    Han, Xiaoliang
    EPIGENOMICS, 2017, 9 (05) : 599 - 610
  • [8] Circulating Methylated SEPT9 DNA in Plasma Is a Biomarker for Colorectal Cancer
    deVos, Theo
    Tetzner, Reimo
    Model, Fabian
    Weiss, Gunter
    Schuster, Matthias
    Distler, Juergen
    Steiger, Kathryn V.
    Gruetzmann, Robert
    Pilarsky, Christian
    Habermann, Jens K.
    Fleshner, Phillip R.
    Oubre, Benton M.
    Day, Robert
    Sledziewski, Andrew Z.
    Lofton-Day, Catherine
    CLINICAL CHEMISTRY, 2009, 55 (07) : 1337 - 1346
  • [9] A systematic review of the performance of the SEPT9 gene methylation assay in colorectal cancer screening, monitoring, diagnosis and prognosis
    Song, Lele
    Yu, Haotian
    Jia, Jia
    Li, Yuemin
    CANCER BIOMARKERS, 2017, 18 (04) : 425 - 432
  • [10] Sept9 DNA Methylation in Healthy, Adenoma and Colorectal Cancer Patients: A Comparison Between Tissue and Plasma Specimens
    Toth, Kinga
    Galamb, Orsolya
    Sipos, Ferenc
    Leiszter, Katalin
    Valcz, Gabor
    Wasserkort, Reinhold
    Tulassay, Zsolt
    Molnar, Bela
    GASTROENTEROLOGY, 2012, 142 (05) : S528 - S529