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. 2020 Sep 2;9(9):2017. doi: 10.3390/cells9092017

Table 2.

Methylation of circulating L1 in blood samples of cancer patients.

Tumor Location Clinical Samples Method Results Ref.
Colorectal
(patients before treatment)
Plasma AQAMA qPCR Significant decrease of L1 MI in cancer patients compared with healthy subjects
Association of L1MI with disease progression (advanced stage and distant metastasis)
[112]
Lung
(patients before treatment)
Cell surface-bound fraction of blood MIRA Significant decrease of L1 MI in cancer patients compared with healthy subjects
Hypomethylation of L1 promoters in cancer patients is more pronounced for the L1 human-specific (L1Hs) family
[115]
Lung
(patients before treatment and after antitumor therapy)
Cell surface-bound fraction of blood qMSP PCR Association of L1 MI with tumor histological type
Dynamic changes in L1 MI of csb-cirDNA during the follow-up period
[117]
Lung
(patients before treatment)
Cell surface-bound fraction of blood, plasma qMSP PCR Significant decrease of L1 MI in csb-cirDNA in cancer patients compared with healthy subjects [116]
Lung
(patients before treatment)
Cell surface-bound fraction of blood, plasma qMSP PCR Decrease of L1 MI in cancer patients compared with the joint control group (healthy subjects + patients with bronchitis + COPD patients) and with COPD patients [118]
Diffuse large B cell lymphoma
(patients before treatment)
Plasma Pyrosequencing Association of L1 hypomethylation with poor overall survival [119]
Melanoma
(patients before treatment)
Serum AQAMA qPCR Decrease of L1 methylation during disease progression (advanced stage) [120]

Abbreviations: MIRA, methylated CpG island recovery assay; AQAMA, absolute quantitative assessment of methylated alleles; qMSP-PCR, quantitative methyl-specific PCR; L1 MI, L1 methylation index; csb-cirDNA, cell surface-bound circulating DNA.