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. 2018 Jul 11;10:1969–1974. doi: 10.2147/CMAR.S169533

Table 2.

Association of NRP1 transcript levels with patients’ clinicopathological data

Variable Number of cases NRP1 high level P-value
Age (years)
 <50 21 (44%) 11 NS
 ≥50 27 (56%) 17
Body mass index (kg/m2)
 25–29 24 (50%) 14 NS
 >29 22 (46%) 13
Menopause status
 Post 37 (77%) 21 NS
 Pre 11 (23%) 7
Stage
 I 11 (23%) 4 NS
 II 18 (37.5%) 14
 III 16 (33%) 6
 IV 3 (6.5%) 2
Histological grade
 I 7 (14.5%) 4 NS
 II 25 (52%) 15
 III 16 (33.5%) 7
Mitotic rate
 1 19 (39.5%) 10 NS
 2 22 (46%) 10
 3 7 (14.5%) 6
Tumor size (cm)
 ≤2 18 (37.5%) 9 NS
 2–5 22 (46%) 12
 ≥5 8 (16.5%) 5
Lymph node involvement
 Positive 19 (39.5%) 10 NS
 Negative 29 (60.5%) 16
HER2
 Positive 25 (75%) 16 NS
 Negative 23 (25%) 10
ER
 Positive 37 (77%) 21 NS
 Negative 11 (23%) 5
PR
 Positive 35 (73%) 19 NS
 Negative 13 (27%) 7
Breast cancer phenotype
 Luminal A 19 (39.5%) 11 0.891
 Luminal B 22 (46%) 13
 HER2 2 (4%) 1
 Triple negative 5 (10.5%) 3

Note: NRP1 high level was defined based on the cut-offs of the fold changes in tumoral tissue vs. the corresponding ANCT, and the median value of fold changes was set as cutoff.

Abbreviations: NRP1, neuropilin-1; ANCT, adjacent noncancerous tissue; HER2, human epidermal growth factor receptor 2; ER, estrogen receptor; PR, progesterone receptor; NS, not significant.