Literature DB >> 25966097

Expression and significance of SATB1 in the development of breast cancer.

S Zhang1, X Gao2, Y Ma2, J Jiang2, Z Dai2, X Yin2, W Min2, W Hui2, B Wang2.   

Abstract

Special AT-rich sequence binding protein 1 (SATB1) is a recently discovered gene regulator that can promote the growth and metastasis of breast cancer. However, its expression in different stages of breast cancer development have not been examined. We explored the role of SATB1 in the development of breast cancer by detecting SATB1 expression levels in different stages of breast cancer. SATB1 expression was determined using an immunohistochemical streptavidin peroxidase method; the relationship between clinicopathological features of breast cancer and SATB1 expression was analyzed using the X(2) test. Positive rates of SATB1 protein in normal breast tissue, normal breast ductal hyperplasia tissue, precancerous lesions of breast cancer, non-invasive cancer, early invasive carcinoma, and invasive breast cancer tissue were, respectively, 6.25 (2/32), 6.4 (3/47), 20.4 (10/49), 45.0 (9/20), 52.9 (9/17), and 76.6% (72/94). SATB1 in the latter 3 groups was significantly higher than in the first 3 groups (P < 0.05). The positive rate of SATB1 protein in invasive non-special types of breast cancer (88.5%, 54/61) was significantly higher than in the special type of invasive breast cancer (54.5%, 18/33) and early invasive breast cancer (52.9%, 9/17) (P < 0.05). SATB1 protein expression in breast cancer with lymph node metastasis was generally increased, and the difference was statistically significant (P < 0.05). SATB1 protein expression showed an increasing trend in different stages of breast cancer development. Overexpression indicated poor prognosis.

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Year:  2015        PMID: 25966097     DOI: 10.4238/2015.April.13.10

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  7 in total

1.  MicroRNA-409 regulates the proliferation and invasion of breast cancer cell lines by targeting special AT-rich sequence-binding protein 1 (SATB1).

Authors:  Zhi Chen; Mei-Xiang Sang; Cui-Zhi Geng; Hui-Qun Jia
Journal:  Bioengineered       Date:  2022-05       Impact factor: 6.832

2.  Downregulation of SATB1 increases the invasiveness of Jurkat cell via activation of the WNT/β-catenin signaling pathway in vitro.

Authors:  Xiao-Dan Luo; Shao-Jiang Yang; Jia-Ni Wang; Li Tan; Dan Liu; Ya-Ya Wang; Run-Hui Zheng; Xiao-Hong Wu; Li-Hua Xu; Huo Tan
Journal:  Tumour Biol       Date:  2015-12-17

3.  High expression of special AT-rich sequence binding protein-1 predicts esophageal squamous cell carcinoma relapse and poor prognosis.

Authors:  Songhui Zhai; Jianxin Xue; Zheng Wang; Lijuan Hu
Journal:  Oncol Lett       Date:  2017-09-27       Impact factor: 2.967

4.  Prognostic and Clinicopathological Significance of SATB1 in Colorectal Cancer: A Meta-Analysis.

Authors:  Jun Zhao; Yajun Tuo; Wei Luo; Shaojun He; Yifei Chen
Journal:  Front Physiol       Date:  2018-05-15       Impact factor: 4.566

5.  FOXA1 Suppresses SATB1 Transcription and Inactivates the Wnt/β-Catenin Pathway to Alleviate Diabetic Nephropathy in a Mouse Model.

Authors:  Hong Zhu; Jiarui Peng; Wei Li
Journal:  Diabetes Metab Syndr Obes       Date:  2021-09-10       Impact factor: 3.168

Review 6.  Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review.

Authors:  Sheng Zhang; Yi Xin Tong; Xiang Shang Xu; Hui Lin; Teng Fei Chao
Journal:  Oncotarget       Date:  2017-07-18

7.  Expression of SATB1 and E-cad in tissues of patients with endometrial carcinoma and the relationship with clinicopathological features.

Authors:  Yanli Feng; Xin Wang; Quanyi Wang
Journal:  Exp Ther Med       Date:  2018-03-13       Impact factor: 2.447

  7 in total

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