We studied interrelationships between the cytoarchitectonics of the mesenteric lymph node and the levels of microRNA-21, microRNA-221/222, and microRNA-429 in the lymph, blood serum, and breast tissues in female Wistar rats with chemically induced breast cancer. After polychemotherapy, significant correlations were found between miRNA-221 and the number of lymphoblasts in the germinal centers and between miRNA-222 and the number of lymphoblasts in the germinal centers and macrophages in the medullary cords of the mesenteric lymph nodes.
Similar content being viewed by others
References
Kabakov AV, Lykov AP, Morozov DV, Kazakov OV, Poveshchenko AF, Raiter TV, Strunkin DN, Konenkov VI. Phenotypical Characteristics of Chemically Induced Mammary Tumor. Bull. Exp. Biol. Med. 2017;163(4):490-492. doi: https://doi.org/10.1007/s10517-017-3835-6
Kazakov OV, Poveshchenko AF, Orlov NB, Reiter TV, Poveshchenko OV, Kabakov AV, Strunkin DN, Lykov AP, Konenkov VI. Relationship between lymph concentration of cytokines and structural transformations in mesenteric lymph nodes in chemotherapy, surgical treatment, and chemotherapy of experimental breast cancer. Patol. Fiziol. Eksp. Ter. 2020;64(2):37-45. doi: https://doi.org/10.25557/0031-2991.2020.02.37-45. Russian.
Chan JA, Krichevsky AM, Kosik KS. MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells. Cancer Res. 2005;65(14):6029-6033. doi: https://doi.org/10.1158/0008-5472.CAN-05-0137
Choi YC, Yoon S, Jeong Y, Yoon J, Baek K. Regulation of vascular endothelial growth factor signaling by miR-200b. Mol Cells. 2011;32(1):77-82. doi: https://doi.org/10.1007/s10059-011-1042-2
Gregory PA, Bert AG, Paterson EL, Barry SC, Tsykin A, Farshid G, Vadas MA, Khew-Goodall Y, Goodall GJ. The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1. Nat. Cell Biol. 2008;10(5):593-601. doi: https://doi.org/10.1038/ncb1722
He L, Hannon GJ. MicroRNAs: small RNAs with a big role in gene regulation. Nat. Rev. Genet. 2004;5(7):522-531. doi: https://doi.org/10.1038/nrg1379
Januszyk P, Januszyk K, Wierzbik-Strońska M, Boroń D, Grabarek B. Analysis of the differences in the expression of mRNAs and miRNAs associated with drug resistance in endometrial cancer cells treated with salinomycin. Curr. Pharm. Biotechnol. 2021;22(4):541-548. doi: https://doi.org/10.2174/1389201021666200629151008
Li J, Guan X, Fan Z, Ching LM, Li Y, Wang X, Cao WM, Liu DX. Non-invasive biomarkers for early detection of breast cancer. Cancers (Basel). 2020;12(10):2767. doi: https://doi.org/10.3390/cancers12102767
Lim YY, Wright JA, Attema JL, Gregory PA, Bert AG, Smith E, Thomas D, Lopez AF, Drew PA, Khew-Goodall Y, Goodall GJ. Epigenetic modulation of the miR-200 family is associated with transition to a breast cancer stem-cell-like state. J. Cell Sci. 2013;126(Pt 10):2256-2266. doi: https://doi.org/10.1242/jcs.122275
Matsuzaki J, Suzuki H. Role of microRNAs-221/222 in digestive systems. J. Clin. Med. 2015;4(8):1566-1577. doi: https://doi.org/10.3390/jcm4081566
Su Z, Jiang G, Chen J, Liu X, Zhao H, Fang Z, He Y, Jiang X, Xu G. MicroRNA-429 inhibits cancer cell proliferation and migration by targeting AKT1 in renal cell carcinoma. Mol. Clin. Oncol. 2020;12(1):75-80. doi: https://doi.org/10.3892/mco.2019.1940
Yuan L, Bing Z, Yan P, Li R, Wang C, Sun X, Yang J, Shi X, Zhang Y, Yang K. Integrative data mining and meta-analysis to investigate the prognostic role of microRNA-200 family in various human malignant neoplasms: A consideration on heterogeneity. Gene. 2019;716:144025. doi: https://doi.org/10.1016/j.gene.2019.144025
Yang CH, Pfeffer SR, Sims M, Yue J, Wang Y, Linga VG, Paulus E, Davidoff AM, Pfeffer LM. The oncogenic microRNA-21 inhibits the tumor suppressive activity of FBXO11 to promote tumorigenesis. J. Biol. Chem. 2015;290(10):6037-6046. doi: https://doi.org/10.1074/jbc.M114.632125
Zhang C, Zhang J, Zhang A, Wang Y, Han L, You Y, Pu P, Kang C. PUMA is a novel target of miR-221/222 in human epithelial cancers. Int. J. Oncol. 2010;37(6):1621-1626. doi: https://doi.org/10.3892/ijo_00000816
Author information
Authors and Affiliations
Corresponding author
Additional information
Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Vol. 172, No. 10, pp. 483-487, October, 2021
Rights and permissions
About this article
Cite this article
Kabakov, A.V., Kazakov, O.V., Poveshchenko, A.F. et al. Correlation between Structural Transformations in Mesenteric Lymph Nodes and the Levels MicroRNA during Polychemotherapy of Breast Cancer. Bull Exp Biol Med 172, 467–471 (2022). https://doi.org/10.1007/s10517-022-05415-4
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10517-022-05415-4