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Recombinant water stress protein 1 (Re-WSP1) suppresses colon cancer cell growth through the miR-539/β-catenin signaling pathway

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Abstract

Background

Nostoc commune Vauch. is a nitrogen-fixing blue-green algae that expresses a large number of active molecules with medicinal properties. Our previous study found that a water stress protein (WSP1) from N. commune and its recombinant counterpart (Re-WSP1) exhibited significant anti-colon cancer activity both in vitro and in vivo. This study is to investigate the effects of Re-WSP1 on proliferation of colon cancer cells and to elucidate the relevant mechanisms.

Methods

Real-time quantitative PCR was used to detect the expression of miR-539 in colon cancer HT-29 and DLD1 cells. Colon cancer cells were transfected with miR-539 mimics and negative controls, and cell proliferation were detected by CCK8 and clonogenic assays. The target gene of miR-539 was predicted, and the dual luciferase reporter gene experiment was used to verify the target gene. After colon cancer cells were transfected with miR-539 mimics or inhibitors, the expression of target gene β-catenin was detected by Western blot. miR-539 inhibitor confirmed cell proliferation.

Results

Re-WSP1 inhibited colon cancer cell growth in a dose-dependent manner. Re-WSP1 inhibited the expression of β-catenin, which was partly reversed by LiCl treatment. Quantitative PCR analysis showed that the expression of miR-539 was significantly upregulated after Re-WSP1 treatment. Moreover, miR-539 negatively regulated the expression of β-catenin by directly binding to the 3′UTR of β-catenin mRNA. The cell growth inhibition and the decrease in β-catenin expression induced by Re-WSP1 were significantly reversed by miR-539 inhibitor.

Conclusion

Re-WSP1 suppresses colon cancer cell growth via the miR-539/β-catenin axis.

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Data availability

The datasets used or analyzed during the current study are available from the corresponding author upon reasonable request.

References

  1. Scherer S, Potts M (1989) Novel water stress protein from a desiccation-tolerant cyanobacterium: purification and partial characterization. J Biol Chem 264(21):12546–53

    Article  CAS  Google Scholar 

  2. Sakamoto T, Kumihashi K, Kunita S et al (2011) The extracellular-matrix-retaining cyanobacterium Nostoc verrucosum accumulates trehalose, but is sensitive to desiccation. FEMS Microbiol Ecol 77(2):385–394

    Article  CAS  Google Scholar 

  3. Guo S-J, Shan S-H, Jin X-T, Li Z-W, Song L, Li Z-Y (2014) Cloning and expression of a novel water stress protein from Nostoc commune Vauch. and its inhibitory effect on the proliferation of human colon cancer SW480 cells. Food Sci 35(13):151–155

    CAS  Google Scholar 

  4. Boyle P, Leon ME (2002) Epidemiology of colorectal cancer. Br Med Bull 64(474):1–25

    Article  Google Scholar 

  5. Yoshida N, Kinugasa T, Ohshima K et al (2015) Analysis of Wnt and β-catenin expression in advanced colorectal cancer. Anticancer Res 35(8):4403–4410

    CAS  PubMed  Google Scholar 

  6. Valinezhad Orang A, Safaralizadeh R, Kazemzadeh-Bavili M (2014) Mechanisms of miRNA-mediated gene regulation from common downregulation to mRNA-specific upregulation. Int J Genomics 2014:970607

    Article  Google Scholar 

  7. Hwang HW, Mendell JT (2007) MicroRNAs in cell proliferation, cell death, and tumorigenesis. Br J Cancer 96:R40-44

    PubMed  Google Scholar 

  8. Dong Y, Yu J, Ng SS (2014) MicroRNA dysregulation as a prognostic biomarker in colorectal cancer. Cancer Manag Res 6:405–422

    PubMed  PubMed Central  Google Scholar 

  9. Zhou JJ, Zheng S, Sun LF, Zheng L (2014) MicroRNA regulation network in colorectal cancer metastasis. World J Biol Chem 5:301–307

    Article  Google Scholar 

  10. Wang P, Meng X, Huang Y, Lv Z, Liu J, Wang G, Meng W, Xue S, Zhang Q, Zhang P, Chen G (2017) MicroRNA-497 inhibits thyroid cancer tumor growth and invasion by suppressing BDNF. Oncotarget 8:2825–2834

    Article  Google Scholar 

  11. Olarewaju OA, Alashi AM et al (2018) Influence of nitrogen fertilizer micro-dosing on phenolic content, antioxidant, and anticholinesterase properties of aqueous extracts of three tropical leafy vegetables. J Food Biochem 42(4):1. https://doi.org/10.1111/jfbc.12566

    Article  CAS  Google Scholar 

  12. Chen J-S, Huang J-Q, Luo B et al (2017) PIK3CD induces cell growth and invasion by activating AKT/GSK-3β/β-catenin signaling in colorectal cancer. Cancer Sci. https://doi.org/10.1111/cas.13931

    Article  PubMed  PubMed Central  Google Scholar 

  13. Yu J, Liu D, Sun X et al (2019) CDX2 inhibits the proliferation and tumor formation of colon cancer cells by suppressing Wnt/β-catenin signaling via transactivation of GSK-3β and Axin2 expression. Cell Death Dis. https://doi.org/10.1038/s41419-018-1263-9

    Article  PubMed  PubMed Central  Google Scholar 

  14. Wu Z, Tang F, Yang B (2018) Ectopic expression of β-catenin in colon cancer and its effect on the proliferation of colon cancer cells. S China J Natl Def Med 32(11):745–748

    Google Scholar 

  15. Bushati N, Cohen SM (2007) microRNA functions. Annu Rev Cell Dev Biol 23:175–205

    Article  CAS  Google Scholar 

  16. Volinia S, Calin GA, Liu CG et al (2006) A microRNA expression signature of human solid tumors defines cancer gene targets. Proc Natl Acad Sci USA 103:2257–2261

    Article  CAS  Google Scholar 

  17. Xing Z, Miao Li, Kai Z et al (2013) Upregulated miR-155 in papillary thyroid carcinoma promotes tumor growth by targeting APC and activating Wnt/beta-catenin signaling. J Clin Endocrinol Metab 98(8):E1305-1313

    Article  Google Scholar 

  18. Zhi Y, Shaofei C, Jian W et al (2015) miR-155 contributes to the progression of glioma by enhancing Wnt/beta-catenin pathway. Tumour Biol 36(7):5323–5331

    Article  Google Scholar 

  19. Yan Z, Wuqing W, Na C et al (2012) Hepatitis C virus-induced up-regulation of microRNA-155 promotes hepatocarcinogenesis by activating Wnt signaling. Hepatology 56(5):1631–1640

    Article  Google Scholar 

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Funding

This research was supported by the Shanxi Province Science Foundation for Youths (201601D021108) and the National Natural Science Foundation of China (No. 81603020).

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All the authors contributed to the collection of references, the contents of the article and the charts.

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Correspondence to Zhuoyu Li.

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Guo, S., Shan, S., Wu, H. et al. Recombinant water stress protein 1 (Re-WSP1) suppresses colon cancer cell growth through the miR-539/β-catenin signaling pathway. Mol Biol Rep 48, 7059–7065 (2021). https://doi.org/10.1007/s11033-021-06549-w

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