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. Author manuscript; available in PMC: 2015 Apr 1.
Published in final edited form as: Sci Signal. 2014 Apr 1;7(319):ra31. doi: 10.1126/scisignal.2004761

Table 1. Clinicopathological characteristics and ASS1 distribution of eligible patients with breast cancer.

No. of cases No. of patients
with low ASS1
abundance (%)*
P
Age (years)
 <40 12 9 (75)
 40–49 53 34 (64.1)
 50–59 43 26 (60.5)
 60–69 23 15 (65.2)
 70–79 14 10 (81.4)
 >80 4 3 (75.0) 0.573
T stage
 T0–T1 36 15 (41.7)
 T2–T4 108 76 (70.4) 0.002
N stage
 N0 72 44 (61.1)
 N1–N3 77 51 (66.2) 0.516
ER
 Negative 52 30 (57.7)
 Positive 73 47 (64.4) 0.448
PR
 Negative 62 30 (48.4)
 Positive 60 43 (71.7) 0.009
Ki-67
 Negative 48 36 (75.0)
 Positive 78 51 (55.3) 0.012
HER2
 Negative 97 63 (64.9)
 Positive 30 14 (46.7) 0.07
Molecular subtype§
 Luminal A 36 27 (75)
 Luminal B 43 26 (60.5)
 TNBC 22 12 (54.5)
 HER2 12 2 (16.7) 0.005
p53
 Negative 62 42 (67.7)
 Positive 61 33 (54.1) 0.12
*

Either no staining or weak cytoplasmic ASS1 staining.

Tumor node metastasis stage is according to AJCC Cancer Staging Manual, 6th Edition.

Statistical significance, P < 0.05.

§

Molecular subtype is categorized according to ER, PR, HER2, and Ki-67 status. Luminal A subtype is defined as ER-positive and/or PR-positive, HER2-negative, and Ki-67–negative; luminal B subtype is defined as ER-positive and/or PR-positive, HER2-negative, and Ki-67–positive; TNBC subtype is defined as ER-negative, PR-negative, and HER2-negative; HER2 subtype is defined as ER-negative, PR-negative, and HER2-positive.