Detection of hypermethylated BCAT1 and IKZF1 DNA in blood and tissues of colorectal, breast and prostate cancer patients

被引:7
|
作者
Winter, Jean M. [1 ,5 ]
Sheehan-Hennessy, Lorraine [1 ,5 ]
Yao, Beibei [1 ]
Pedersen, Susanne K. [2 ]
Wassie, Molla M. [1 ,5 ]
Eaton, Michael [3 ]
Chong, Michael [4 ]
Young, Graeme P. [1 ]
Symonds, Erin L. [1 ,5 ]
机构
[1] Flinders Univ South Australia, Coll Med & Publ Hlth, Flinders Hlth & Med Res Inst, Canc Res, Bedford Pk, SA, Australia
[2] Clin Genom Pty Ltd, N Ryde, NSW, Australia
[3] Flinders Med Ctr, Flinders Breast Canc Unit, Bedford Pk, SA, Australia
[4] Flinders Med Ctr, Urol Serv, Bedford Pk, SA, Australia
[5] Flinders Med Ctr, Bowel Hlth Serv, Bedford Pk, SA, Australia
关键词
ctDNA; biomarker; DNA methylation; bowel cancer; sensitivity; specificity; diagnostic accuracy; METHYLATION; GROWTH; PROMOTES;
D O I
10.3233/CBM-210399
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Detection of circulating cell-free DNA (ccfDNA) methylated in BCAT1 and IKZF1 is sensitive for detection of colorectal cancer (CRC), but it is not known if these biomarkers are present in other common adenocarcinomas. OBJECTIVE: Compare methylation levels of BCAT1 and IKZF1 in tissue and plasma from breast, prostate, and colorectal cancer patients. METHODS: Blood was collected from 290 CRC, 32 breast and 101 prostate cancer patients, and 606 cancer-free controls. Tumor and matched normal tissues were collected at surgery: 26 breast, 9 prostate and 15 CRC. DNA methylation in BCAT1 and IKZF1 was measured in blood and tissues. RESULTS: Either biomarker was detected in blood from 175/290 (60.3%) of CRC patients. The detection rate was higher than that measured in controls (48/606 (8.1%), OR = 18.2, 95%CI: 11.1-29.0). The test positivity rates in breast and prostate cancer patients were 9.4% (3/32) and 6.9% (7/101), respectively, and not significantly different to that measured in gender-matched controls (8.0% (33/382) females (OR = 0.84, 95%CI: 0.23-3.1) and 7.6% (26/318) males (OR = 0.86, 95%CI: 0.65-2.1). In tumor and non-neoplastic tissues, 93.5% (14/15) of CRC tumors were methylated in BCAT1 and/or IKZF1 (p < 0.004). Only 11.5% (3/26) and 44.4% (4/9) (p = 0.083) of breast and prostate tumors were hypermethylated in these two genes. CONCLUSIONS: Detection of circulating DNA methylated in BCAT1 and IKZF1 is sensitive and specific for CRC but not breast or prostate cancer.
引用
收藏
页码:493 / 503
页数:11
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