CRM1, a novel independent prognostic factor overexpressed in invasive breast carcinoma of poor prognosis.
CRM1, a novel independent prognostic factor overexpressed in invasive breast carcinoma of poor prognosis.
复制标题
CRM1,一种在预后不良的浸润性乳腺癌中过度表达的新型独立预后因素
DOI:
10.3892/ol.2018.8316
复制
发表时间:
2018-05
期刊:
影响因子:
2.9
通讯作者:
Niu HT
中科院分区:
文献类型:
--
作者:
Yue L;Sun ZN;Yao YS;Shen Z;Wang HB;Liu XP;Zhou F;Xiang JY;Yao RY;Niu HT
Breast cancer (BC) is the most commonly diagnosed cancer in females globally and is more aggressive at later stages. Chromosome region maintenance 1 (CRM1) is involved in the nuclear export of proteins and RNAs and has been associated with a number of malignancies. However, the clinicopathological significance of its expression in BC remains to be elucidated therefore this was investigated in the present study. CRM1 expression in 280 breast cancer tissues and 60 normal tissues was retrospectively analyzed using immunohistochemistry (IHC) and western blotting. IHC investigation demonstrated that CRM1 expression was significantly increased in BC compared with the normal breast epithelium (P<0.0001). Overexpression of CRM1 was markedly associated with poor prognostic characteristics, including larger tumor size (P=0.024), positive lymph node metastasis (P=0.032), invasive histological type (P=0.004) and distant metastasis (P=0.026). Significant associations were also observed between increased CRM1 expression and the progesterone receptor (P=0.028) and Ki67 (P=0.019). Kaplan-Meier survival analysis demonstrated that patients with high CRM1 expression exhibited a reduced disease-free survival and overall survival compared with those with low CRM1 expression (P=0.013). In the multivariate analysis, CRM1 expression (P=0.011), tumor size (P=0.001) and lymph node metastasis (P<0.001) were independent prognostic markers of BC. In conclusion, CRM1 serves an important role in BC and may serve as a predictive and prognostic factor for a poor outcome in patients with BC.
登录
查看更多内容
影响因子:
28.5
作者:
Parikh K;Cang S;Sekhri A;Liu D
通讯作者:
Liu D
影响因子:
64.5
作者:
Fornerod, M;Ohno, M;Mattaj, IW
通讯作者:
Mattaj, IW
影响因子:
29.4
作者:
Azmi AS;Aboukameel A;Bao B;Sarkar FH;Philip PA;Kauffman M;Shacham S;Mohammad RM
通讯作者:
Mohammad RM
影响因子:
4.8
作者:
Shen, Aiguo;Wang, Yuchan;Cheng, Chun
通讯作者:
Cheng, Chun
DOI:
10.1073/pnas.96.16.9112
发表时间:
1999-08-03
影响因子:
11.1
作者:
Kudo, N;Matsumori, N;Horinouchi, S
通讯作者:
Horinouchi, S