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Table 1 Clinicopathological features of the TCGA breast adenocarcinomas

From: Large-scale analysis of DFNA5 methylation reveals its potential as biomarker for breast cancer

Clinicopathological parameter

Methylation (N = 668)

Expression–microarray (N = 476)

Expression–RNA-seq (N = 666)

Number (%)

P value (range)

Number (%)

P value

Number (%)

P value

ER

 

2.2 × 10−22–0.049 (20/22 CpGs)

 

0.038

 

3.3 × 10− 3

 ER+

490 (73.3)

 

362 (76.0)

 

488 (73.3)

 

 ER−

142 (21.3)

 

107 (22.5)

 

142 (21.3)

 

 Unknown

36 (5.4)

 

7 (1.5)

 

36 (5.4)

 

PR

 

9.7 × 10−15–3.0 × 10−3 (15/22 CpGs)

 

N.S.

 

N.S.

 PR+

428 (64.1)

 

310 (65.1)

 

427 (64.1)

 

 PR−

201 (30.1)

 

158 (33.2)

 

200 (30.0)

 

 Unknown

39 (5.8)

 

8 (1.7)

 

39 (5.9)

 

HER2

 

0.023 (1/22 CpGs)

 

N.S.

 

N.S.

 HER2+

32 (4.8)

 

45 (9.4)

 

32 (4.8)

 

 HER2−

195 (29.2)

 

166 (34.9)

 

195 (29.3)

 

 Unknown

441 (66.0)

 

265 (55.7)

 

439 (65.9)

 

Tumor stage

 

1.9 × 10−4–0.020 (5/22 CpGs)

 

N.S.

 

N.S.

 I

109 (16.3)

 

83 (17.5)

 

107 (16.1)

 

 II

378 (56.6)

 

269 (56.5)

 

378 (56.8)

 

 III

166 (24.9)

 

99 (20.8)

 

166 (24.9)

 

 IV

9 (1.3)

 

12 (2.5)

 

9 (1.3)

 

 Unknown

6 (0.9)

 

13 (2.7)

 

6 (0.9)

 

Histological diagnosis

 

1.0 × 10−4–0.038 (10/22 CpGs)

 

4.2 × 10−4

 

3.2 × 10−4

 Ductal

496 (74.3)

 

435 (91.4)

 

494 (74.2)

 

 Lobular

172 (25.7)

 

41 (8.6)

 

172 (25.8)

 
  1. Important clinicopathological parameters, such as ER status, PR status, HER2 status, tumor stage (I–IV), and histological diagnosis are reported for the breast adenocarcinomas. The numbers of adenocarcinomas in each category are reported for the methylation and expression (both microarray and RNA-seq) dataset. The significant p values for the association analysis with either DFNA5 methylation, DFNA5 microarray expression, or DFNA5 RNA-seq expression are reported
  2. N.S. not significant