Antiproliferative Effect of Mesenchymal Stem Cells on Human Breast Carcinoma: New Insight on FOXO/lncRNA-AF085935 Axis

Authors

  • Sahar H. Ahmed Department of Medical Laboratory Technology https://orcid.org/0000-0002-0436-5053
  • Abeer Mostafa Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Cairo University, Cairo, Egypt
  • Amany A. Abou-Elalla Department of Medical Laboratory Technology

DOI:

https://doi.org/10.3889/oamjms.2021.6814

Keywords:

Breast carcinoma, Mesenchymal stem cells, Interleukin-6, Nuclear factor-kappa B, TLR4 and FOXO/LncRNA AF085935 axis

Abstract

AIM: Cancer breast is one of the most common cancer in women leading to death; that is why we are in urgent need to develop new modalities of treatment. Mesenchymal stem cells (MSCs) have an anti-inflammatory effect due to capability to regenerate the damaged tissues.

METHODS: MCF7 breast cancer cells were divided into two groups; group 1: untreated cancer cells, group 2: cancer cell cocultured with MSCs; after 24 incubation the cells from the two groups were collected to assess cell proliferation, Interleukin-6 (IL-6) levels and genes expression of Nuclear factor-kappa B (NF-KB), FOXO, and LncRNA AF085935.

RESULTS: Statistically significant decrease in cancer cell proliferation and all other studied parameters in cancer cells after coculture with MSCs.

CONCLUSION: Breast carcinoma once initiated; it runs in a vicious circle due to stimulation of FOXO/LncRNA AF085935 axis by the inflammatory mediators released from cancer environment. FOXO/LncRNA AF085935 induces cancer proliferation and survival; furthermore, FOXO once induced, it produces further induction of inflammatory cytokines IL-6 and NF-KB and so on, MSCs due to its anti-inflammatory role could break this circle and thus inhibit cancer cell proliferation.

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References

Muscatell KA, Eisenberger NI, Dutcher JM, Cole SW, Bower JE. Links between inflammation, amygdala reactivity, and social support in breast cancer survivors. Brain Behav Immun. 2016;53:34-8. https://doi.org/10.1016/j.bbi.2015.09.008 PMid:26384778 DOI: https://doi.org/10.1016/j.bbi.2015.09.008

Zhao S, Zhang Y, Zhang Q, Wang F, Zhang D. Toll-like receptors and prostate cancer. Front Immunol. 2014;5:352. https://doi.org/10.3389/fimmu.2014.00352 PMid:25101092 DOI: https://doi.org/10.3389/fimmu.2014.00352

Wang X, Li X, Zhang X, Zang L, Yang H, Zhao W, et al. Toll-like receptor 4-induced inflammatory responses contribute to the tumor-associated macrophages formation and infiltration in patients with diffuse large B-cell lymphoma. Ann Diagn Pathol 2015;19(4):232-8. https://doi.org/10.1016/j.anndiagpath.2015.04.008 PMid:26071054 DOI: https://doi.org/10.1016/j.anndiagpath.2015.04.008

Dabagh-Gorjani F, Anvari F, Zolghadri J, Kamali-Sarvestani E, Gharesi-Fard B. Differences in the expression of TLRs and inflammatory cytokines in pre-eclamptic compared with healthy pregnant women. Iran J Immunol. 2014;11(4):233-45. https://doi.org/10.1016/j.placenta.2009.11.004 PMid:25549591 DOI: https://doi.org/10.1016/j.placenta.2009.11.004

Matijevic T, Pavelic J. Toll-like receptors: Cost or benefit for cancer? Curr Pharm Des 2010;16(9):1081-90. https://doi.org/10.2174/138161210790963779 PMid:20030618 DOI: https://doi.org/10.2174/138161210790963779

Sabry D, Mostafa A, Hassouna A. Breast carcinoma is a multifactorial disease involving FOXN3, SINA3 and NEAT through repression of GATA3 and TJP. J Thorac Dis. 2018;10(3):1167-71. https://doi.org/10.21037/jtd.2018.02.65 PMid:29707264 DOI: https://doi.org/10.21037/jtd.2018.02.65

Zhao Y, Guo Q, Chen J, Hu J, Wang S, Sun Y. Role of long non-coding RNA HULC in cell proliferation, apoptosis and tumor metastasis of gastric cancer: A clinical and in vitro investigation. Oncol Rep. 2014;31(1):358-64. https://doi.org/10.3892/or.2013.2850 PMid:24247585 DOI: https://doi.org/10.3892/or.2013.2850

Bolha L, Ravnik-Glavač M, Glavač D. Long noncoding RNAs as biomarkers in cancer. Dis Markers 2017;2017:7243968. https://doi.org/10.1155/2017/7243968 DOI: https://doi.org/10.1155/2017/7243968

Chulpanova DS, Kitaeva KV, Tazetdinova LG, James V, Rizvanov AA, Solovyeva VV. Application of mesenchymal stem cells for therapeutic agent delivery in anti-tumor treatment. Front Pharmacol. 2018;9:259. https://doi.org/10.3389/fphar.2018.00259 PMid:29615915 DOI: https://doi.org/10.3389/fphar.2018.00259

Weiss ML, Medicetty S, Bledsoe AR, Rachakatla RS, Choi M, Merchav S, et al. Human umbilical cord matrix stem cells: preliminary characterization and effect of transplantation in a rodent model of Parkinson’s disease. Stem Cells. 2006;24(3):781-92. https://doi.org/10.1634/stemcells.2005-0330 PMid:16223852 DOI: https://doi.org/10.1634/stemcells.2005-0330

Deshmukh SK, Srivastava SK, Dyess TP, Holliday NP, Singh AP. Inflammation, immunosuppressive microenvironment and breast cancer: Opportunities for cancer prevention and therapy. Ann Transl Med. 2019;7(20):593. https://doi.org/10.21037/atm.2019.09.68 PMid:31807574 DOI: https://doi.org/10.21037/atm.2019.09.68

Dethlefsen C, Højfeldt G, Hojman P. The role of intratumoral and systemic IL-6 in breast cancer. Breast Cancer Res Treat. 2013;138(3):657-64. https://doi.org/10.1007/s10549-013-2488-z PMid:23532539 DOI: https://doi.org/10.1007/s10549-013-2488-z

Xia Y, Shen S, Verma IM. NF-κB, an active player in human cancers. Cancer Immunol Res. 2014;2(9):823-30. https://doi.org/10.1158/2326-6066.cir-14-0112 DOI: https://doi.org/10.1158/2326-6066.CIR-14-0112

Scherzad A, Steber M, Gehrke T, Rak K, Froelich K, Schendzielorz P, et al. Human mesenchymal stem cells enhance cancer cell proliferation via IL-6 secretion and activation of ERK1/2. Int J Oncol. 2015;47(1):391-7. https://doi.org/10.3892/ijo.2015.3009 PMid:25997536 DOI: https://doi.org/10.3892/ijo.2015.3009

Bhatelia K, Singh K, Singh R. TLRs: Linking inflammation and breast cancer. Cell Signal. 2014;26:2350-7. https://doi.org/10.1016/j.cellsig.2014.07.035 PMid:25093807 DOI: https://doi.org/10.1016/j.cellsig.2014.07.035

Luddy KA, Robertson-Tessi M, Tafreshi NK, Soliman H, Morse DL. The role of toll-like receptors in colorectal cancer progression: Evidence for epithelial to leucocytic transition. Front Immunol. 2014;5:429. https://doi.org/10.3389/fimmu.2014.00429 PMid:25368611 DOI: https://doi.org/10.3389/fimmu.2014.00429

Bhattacharya D, Yusuf N. Expression of toll-like receptors on breast tumors: Taking a toll on tumor microenvironment. Int J Breast Cancer 2012;2012:716564. https://doi.org/10.1155/2012/716564 PMid:22295250 DOI: https://doi.org/10.1155/2012/716564

Mostafa A, Ibrahim NE, Sabry D, Fathy W, Elkazaz AY. Insulin-like growth factor initiates hepatocellular carcinoma in chronic hepatitis C virus patients through induction of long non-coding ribonucleic acids AF085935: Role of LncRNA AF085935 in HCC development. Open Access Maced J Med Sci. 2021;9:222-8. https://doi.org/10.3889/oamjms.2021.5909 DOI: https://doi.org/10.3889/oamjms.2021.5909

Fan W, Morinaga H, Kim JJ, Bae E, Spann NJ, Heinz S, et al. FoxO1 regulates Tlr4 inflammatory pathway signalling in macrophages. EMBO J. 2010;29(24):4223-36. https://doi.org/10.1038/emboj.2010.268 PMid:21045807 DOI: https://doi.org/10.1038/emboj.2010.268

Ito Y, Daitoku H, Fukamizu A. Foxo1 increases pro-inflammatory gene expression by inducing C/EBPbeta in TNF-alpha-treated adipocytes. Biochem Biophys Res Commun. 2009;378(2):290-5. https://doi.org/10.1016/j.bbrc.2008.11.043 PMid:19026986 DOI: https://doi.org/10.1016/j.bbrc.2008.11.043

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Published

2021-09-12

How to Cite

1.
Ahmed SH, Mostafa A, Abou-Elalla AA. Antiproliferative Effect of Mesenchymal Stem Cells on Human Breast Carcinoma: New Insight on FOXO/lncRNA-AF085935 Axis. Open Access Maced J Med Sci [Internet]. 2021 Sep. 12 [cited 2024 Apr. 20];9(A):748-52. Available from: https://oamjms.eu/index.php/mjms/article/view/6814