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. Author manuscript; available in PMC: 2010 Nov 1.
Published in final edited form as: Cancer Causes Control. 2009 Nov;20(9):1539–1550. doi: 10.1007/s10552-009-9415-y

Table 2.

Characteristics of Selected Studies of Promoter Methylation Detected in Circulation

Reference Sample Type and Size Genes Methylation Frequency Coverage A
Hoque et al (66)B Plasma
Cases
(n=47)
GSTP1
RARβ2
RASSF1A
APC
26%
26%
32%
17%
62%
Plasma
Healthy Controls
(n=38)
GSTP1
RARβ2
RASSF1A
APC
0
8%
5%
0
Müller et al (67)B Serum
Cases
Primary tumors
(n=26)
ESR1
APC
HSD17β4
HIC1
RASSF1A
27%
23%
12%
39%
23%
Not Calculated
Recurrent breast cancers
(n=10)
ESR1
APC
HSD17β4
HIC1
RASSF1A
70%
80%
30%
90%
80%
Healthy Controls
(n=10)
ESR1
APC
HSD17β4
HIC1
RASSF1A
0
0
0
10%
10%
Papadopoulou et al (68)B Plasma
Cases
(n=50)
RASSF1A
ATM
26%
14%
36%
Healthy Controls
(n=14)
(n=9)
RASSF1A
ATM
0
0
Tan et al (69)C Serum
Cases
Metastatic
(n=19)
RUNX3
p16
RASSF1A
CDH1
47%
37%
42%
0
79%
Control
(n=10)
All genes 0
A

Coverage, percentage of cases having methylation of at least one gene in the given gene panel (i.e. coverage of 100% means that all samples had methylation of at least one gene in the study’s panel).

B

Methylation analysis was conducted using quantitative real-time methylation specific PCR (QMSP).

C

Methylation analysis was conducted using methylation specific PCR (MSP).