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

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Tumor Biology

Abstract

Special AT-rich sequence-binding protein-1 (SATB1) is critical for genome organizer that reprograms chromatin organization and transcription profiles, and associated with tumor growth and metastasis in several cancer types. Many studies suggest that SATB1 overexpression is an indicator of poor prognosis in various cancers, such as breast cancer, malignant cutaneous melanoma, and liver cancer. However, their expression patterns and function values for adult T cell leukemia (ATL) are still largely unknown. The aim of this study is to examine the levels of SATB1 in ATL and to explore its function and mechanisms in Jurkat cell line. Here, we reported that SATB1 expressions were decreased in ATL cells (p < 0.001) compared with normal controls. Knockdown of SATB1 expression significantly enhanced invasion of Jurkat cell in vitro. Furthermore, knockdown of SATB1 gene enhances β-catenin nuclear accumulation and transcriptional activity and thus may increase the invasiveness of Jurkat cell through the activation of Wnt/β-catenin signaling pathway in vitro.

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Acknowledgments

This study was supported by grants from the National Natural Science Foundation of China (81200399), Key Clinical Disciplines of Guangdong Province (20111219), Guangdong Province Natural Science Foundation (2015A030310126), and Guangzhou Medical and Health Technology Program (20151A011068).

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Correspondence to Li-Hua Xu or Huo Tan.

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Xiao-Dan Luo and Shao-Jiang Yang contributed equally to this work.

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Luo, XD., Yang, SJ., Wang, JN. et al. Downregulation of SATB1 increases the invasiveness of Jurkat cell via activation of the WNT/β-catenin signaling pathway in vitro. Tumor Biol. 37, 7413–7419 (2016). https://doi.org/10.1007/s13277-015-4638-x

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  • DOI: https://doi.org/10.1007/s13277-015-4638-x

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