| Literature DB >> 32965167 |
Hui Liu1, Jianming Chen2, Haifeng Chen2, Jie Xia1, Ouxi Wang1, Jiajing Xie1, Meifeng Li1, Zheng Guo1, Guoping Chen2, Haidan Yan1.
Abstract
Accurate diagnosis of the origin of brain metastases (BMs) is crucial for tailoring an effective therapy to improve patients' prognosis. BMs of unknown origin account for approximately 2-14% of patients with BMs. Hence, the aim of this study was to identify the original cancer type of BMs based on their DNA methylation profiles. The DNA methylation profiles of glioma (GM), BM, and seven other types of primary cancers were collected. In comparison with GM, the reversal CpG site pairs were identified for each of the seven other types of primary cancers based on the within-sample relative methylation orderings (RMOs) of the CpG sites. Then, using the reversal CpG site pairs, GMs were distinguished from BMs and the seven other types of primary cancers. All 61 of the GM samples were correctly identified as GM. The cancer type was also identified for the non-GM samples. For the seven other types of primary cancers, greater than 93% of samples of each cancer type were correctly identified as their corresponding cancer type, except for breast cancer, which had an 88% accuracy. For 133 BM samples, 132 BM samples were identified as non-GM, and 95% of the 133 BM samples were correctly classified into their corresponding original cancer types. The RMO-based method can accurately identify the origin of BMs, which is important for precision treatment.Entities:
Keywords: Brain metastases; DNA methylation; Origin; Primary cancer; Relative methylation orderings
Mesh:
Year: 2020 PMID: 32965167 PMCID: PMC8331033 DOI: 10.1080/15592294.2020.1827720
Source DB: PubMed Journal: Epigenetics ISSN: 1559-2294 Impact factor: 4.528