Acta Scientific Women's Health (ASWH)(ISSN: 2582-3205)

Research Article Volume 3 Issue 10

Bone Marrow Mesenchymal Stem Cells (BMSC)-upregulated miR-139 Inhibited the Migration and Invasion of Breast Cancer Cells In Vitro by Inhibiting PXN Expression and EMT

Liandi Shen1, Mengdi Niu2, Yangyong Lu2, Weihong Cao3 and Xueqiang Gao3*

1Department of Maternal and Child Health, Jiading Maternal and Child Health Hospital, Shanghai, China
2Department of Breast and Thyroid, Qingdao Women and Children's Hospital, Qingdao, Shandong, China
3Department of Breast Disease Clinic, Qingdao University Hospital, Qingdao, Shandong, China

*Corresponding Author: Xueqiang Gao, Department of Breast Disease Clinic, Qingdao University Hospital, Qingdao, Shandong, China.

Received: July 30, 2021; Published: September 20, 2021

Abstract

  Short non-coding RNAs (microRNAs) is reported to exerted a crucial impact in tumor biology. While, the biological effect of miR-139 in breast cancer cells remain unclear yet. Here we intend to clarify the effect and mechanism of miR-139 derived from Bone marrow mesenchymal stem cells (BMSCs) on the biological behavior of gastric cancer cells. Breast cancer cells were divided into BMSC group (mixed culture of BMSC and breast cancer cells 1:1). Cells in the miR-139 mimics group, si-PXN group and control group were not treated. miR-139 abundance is evalued through Real time PCR, cell activity is analysed by MTT assay.Finally, the targeted binding of miR-139 to PXN was verified by double luciferase reporter genes. In relative to control, miR-139 abundance was notably declined in gastric cancer cells, while PXN abundance was higher, and the higher expression of PXN was linked to the prognosis of patients. miR-139 can be up-regulated by BMSCs or miR-139 mimics, thereby regulating EMT process through targeted inhibition of PCN, and ultimately inhibiting in vitro activity of breast cancer cells. BMSC co-culture can inhibit PCN by up-regulating miR-139, thus regulating EMT process and inhibiting the progression of gastric cancer. The results of this study revealed the mechanism of breast cancer progression to a certain extent, and suggested that miR-139 and PXN could be used as therapeutic targets for metastatic breast cancer, and BMSC could be of great value as a novel biologic therapy.

Keywords: Gastric Cancer; MiR – 139; Cell Proliferation; Cell Invasion

References

  1. HARBECK N., et al. “Breast cancer”. Nature Reviews Disease Primers1 (2019): 66.
  2. KATO M., et al. “The mir-34 microRNA is required for the DNA damage response in vivo in C. elegans and in vitro in human breast cancer cells”. Oncogene 25 (2009): 2419-2424.
  3. BEUZELIN D and KAEFFER B. “Exosomes and miRNA-Loaded Biomimetic Nanovehicles, a Focus on Their Potentials Preventing Type-2 Diabetes Linked to Metabolic Syndrome”. Frontiers in Immunology 9 (2018): 2711.
  4. FLESHNER M and CRANE C R. “Exosomes, DAMPs and miRNA: Features of Stress Physiology and Immune Homeostasis”. Trends in Immunology10 (2020): 768-776.
  5. SENGUPTA V., et al. “Exosomes Derived from Bone Marrow Mesenchymal Stem Cells as Treatment for Severe COVID-19”. Stem Cells and Development12 (2020): 747-754.
  6. ZHAO C., et al. “Exosomes from adipose‑derived stem cells promote chondrogenesis and suppress inflammation by upregulating miR‑145 and miR‑221”. Molecular Medicine Reports4 (2020): 1881-1889.
  7. CUI Y., et al. “Shrimp miR-34 from Shrimp Stress Response to Virus Infection Suppresses Tumorigenesis of Breast Cancer”. Molecular Therapy Nucleic Acids 9 (2017): 387-398.
  8. HUANG H Z., et al. “Up-regulation of microRNA-136 induces apoptosis and radiosensitivity of esophageal squamous cell carcinoma cells by inhibiting the expression of MUC1”. Experimental and Molecular Pathology 110 (2019): 104278.
  9. MA C., et al. “Therapeutic effects of bone mesenchymal stem cells on oral and maxillofacial defects: a novel signaling pathway involving miR-31/CXCR4/Akt axis”. Journal of Receptor and Signal Transduction Research4 (2019): 321-330.
  10. LI H C., et al. “Loss of the Opa interacting protein 5 inhibits breast cancer proliferation through miR-139-5p/NOTCH1 pathway”. Gene 603 (2017): 1-8.
  11. WATANABE K., et al. “Histone methylation-mediated silencing of miR-139 enhances invasion of non-small-cell lung cancer”. Cancer Medicine10 (2015): 1573-1582.
  12. WANG Y., et al. “ETV4 overexpression promotes progression of non-small cell lung cancer by upregulating PXN and MMP1 transcriptionally”. Molecular Carcinogenesis1 (2020): 73-86.
  13. LISIAK N., et al. “Semisynthetic oleanane triterpenoids inhibit migration and invasion of human breast cancer cells through downregulated expression of the ITGB1/PTK2/PXN pathway”. Chemico-biological Interactions 268 (2017): 136-147.
  14. NAM R K., et al. “Mir-139 Regulates Autophagy in Prostate Cancer Cells Through Beclin-1 and mTOR Signaling Proteins”. Anticancer Research12 (2020): 6649-6663.
  15. FAN G., et al. “miR-139 inhibits osteosarcoma cell proliferation and invasion by targeting ROCK1”. Frontiers in Bioscience (Landmark edition) 24 (2019): 1167-1177.
  16. SP N., et al. “Nobiletin Inhibits Angiogenesis by Regulating Src/FAK/STAT3-Mediated Signaling through PXN in ER⁺ Breast Cancer Cells”. International Journal of Molecular Sciences5 (2017).
  17. DE FRANCESCO E M and MAGGIOLINI M. “Crosstalk between Notch, HIF-1α and GPER in Breast Cancer EMT”. 19.7 (2018).
  18. VERGARA D., et al. “The Cancer Microbiota: EMT and Inflammation as Shared Molecular Mechanisms Associated with Plasticity and Progression”. Journal of Oncology 2019 (2019): 1253727.
  19. BOULDING T., et al. “LSD1 activation promotes inducible EMT programs and modulates the tumour microenvironment in breast cancer”. Scientific Reports1 (2018): 73.
  20. BAFFY G. “Gut Microbiota and Cancer of the Host: Colliding Interests”. Advances in Experimental Medicine and Biology 1219 (2020): 93-107.
  21. CHI Y., et al. “miR-516a-3p inhibits breast cancer cell growth and EMT by blocking the Pygo2/Wnt signalling pathway”. Journal of Cellular and Molecular Medicine9 (2019): 6295-6307.
  22. LI J., et al. “Targeting the Notch1 oncogene by miR-139-5p inhibits glioma metastasis and epithelial-mesenchymal transition (EMT)”. BMC Neurology1 (2018): 133.
  23. LIU S C., et al. “Ovatodiolide suppresses nasopharyngeal cancer by targeting stem cell-like population, inducing apoptosis, inhibiting EMT and dysregulating JAK/STAT signaling pathway”. Phytomedicine : International Journal of Phytotherapy and Phytopharmacology 56 (2019): 269-278.
  24. OKADA R., et al. “Regulation of Oncogenic Targets by the Tumor-Suppressive miR-139 Duplex (miR-139-5p and miR-139-3p) in Renal Cell Carcinoma”. 8.12 (2020).
  25. WU G., et al. “Up-regulation of SNHG6 activates SERPINH1 expression by competitive binding to miR-139-5p to promote hepatocellular carcinoma progression”. Cell Cycle12 (2019): 6649-6663.

Citation

Citation: Xueqiang Gao., et al. “Bone Marrow Mesenchymal Stem Cells (BMSC)-upregulated miR-139 Inhibited the Migration and Invasion of Breast Cancer Cells In Vitro by Inhibiting PXN Expression and EMT". Acta Scientific Women's Health 3.10 (2021): 03-10.

Copyright

Copyright: © 2021 Xueqiang Gao., et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.




Metrics

Acceptance rate35%
Acceptance to publication20-30 days

Indexed In





News and Events


  • Certification for Review
    Acta Scientific certifies the Editors/reviewers for their review done towards the assigned articles of the respective journals.
  • Submission Timeline for Upcoming Issue
    The last date for submission of articles for regular Issues is July 10, 2024.
  • Publication Certificate
    Authors will be issued a "Publication Certificate" as a mark of appreciation for publishing their work.
  • Best Article of the Issue
    The Editors will elect one Best Article after each issue release. The authors of this article will be provided with a certificate of "Best Article of the Issue"
  • Welcoming Article Submission
    Acta Scientific delightfully welcomes active researchers for submission of articles towards the upcoming issue of respective journals.

Contact US