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[Expression of PTEN protein and its correlation with p27kip1 and cyclin D1 expression in primary breast cancer].

作者信息

Lin Qin, Zhuang Yan-zhen, Xu Dong-po, Ye Jian-xin, Chen Pei-qiong

机构信息

Xiamen First Hospital, Xiamen 361003, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2003 May;25(3):246-9.

PMID:12839686
Abstract

OBJECTIVE

To study the expression of phosphatase and tensin homology deleted on chromosometen ten (PTEN) protein, a tumor suppressor gene in breast cancer and its correlation with p27(kip1) and cyclin D1 expression.

METHODS

PTEN protein expression, p27(kip1) and cyclin D1 protein expression were detected by immunohistochemical method in paraffin sections from 61 women with primary breast cancer. PTEN protein expression was compared with clinico-pathologic parameters as related to p27(kip1) and cyclin D1.

RESULTS

PTEN, being shown in the cytoplasm, was negative in 6.6% (4/61), reduced in 41.0% (25/61) and positive in 52.5% (32/61) samples. PTEN expression level was correlated with axillary lymph node status, loss of estrogen receptor stain, recurrence and metastasis. On univariate analysis, the disease-free survival rate of patients with higher PTEN expression (> 50% cells stained) was better than those with lower expression (P = 0.0101). However, there was no correlation between p27(kip1), cyclin D1 expression or PTEN expression.

CONCLUSION

PTEN, its lower expression being correlated with poor outcome of breast cancer patients, plays a prominent role in breast cancer. p27(kip1) or cyclin D1 may not be the primary downstream genes of PTEN in breast cancer.

摘要

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引用本文的文献

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Medicine (Baltimore). 2017 Sep;96(36):e8000. doi: 10.1097/MD.0000000000008000.
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Expression of PIK3CA, PTEN mRNA and PIK3CA mutations in primary breast cancer: association with lymph node metastases.原发性乳腺癌中PIK3CA、PTEN mRNA的表达及PIK3CA突变:与淋巴结转移的关系
Springerplus. 2013 Sep 16;2(1):464. doi: 10.1186/2193-1801-2-464. eCollection 2013.
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Inhibition of transfected PTEN on human colon cancer.
转染的PTEN对人结肠癌的抑制作用。
World J Gastroenterol. 2004 Dec 15;10(24):3670-3. doi: 10.3748/wjg.v10.i24.3670.