Literature DB >> 31201625

The Expression Level of S100A4 Protein Affects the Migration Activity of Breast Cancer Cells.

E A Dukhanina1, T N Portseva2, A P Kotnova1, E V Pankratova1, S G Georgieva1.   

Abstract

Reduced expression of metastatic marker protein S100A4 in triple-negative breast cancer cells MDA-MB-231 leads to a decrease in the migration ability of cells and increases the sensitivity of the modified cells to docetaxel therapy. Cells capable of migration differ from the immotile cells in the content of the S100A4 protein in the cell, and this difference persists after the treatment of cells with the agents that reduce the intracellular level of S100A4. The presence of exogenous S100A4 protein in culture medium reduces the content of this protein in breast cancer cells. The results of the study show that the ability of breast cancer cells to migrate depends on the S100A4 protein concentration in the cell.

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Year:  2019        PMID: 31201625     DOI: 10.1134/S1607672919020030

Source DB:  PubMed          Journal:  Dokl Biochem Biophys        ISSN: 1607-6729            Impact factor:   0.788


  8 in total

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Authors:  E A Dukhanina; T N Portseva; A S Dukhanin; S G Georgieva
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5.  Oct-1 modifies S100A4 exchange between intra- and extracellular compartments in Namalwa cells and increases their sensitivity to glucocorticoids.

Authors:  Elena A Dukhanina; Tatiana N Portseva; Elizaveta V Pankratova; Natalia V Soshnikova; Alexander G Stepchenko; Alexander S Dukhanin; Sofia G Georgieva
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7.  Anticlusterin treatment of breast cancer cells increases the sensitivities of chemotherapy and tamoxifen and counteracts the inhibitory action of dexamethasone on chemotherapy-induced cytotoxicity.

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Journal:  Breast Cancer Res       Date:  2007       Impact factor: 6.466

8.  Downregulation of AKT3 Increases Migration and Metastasis in Triple Negative Breast Cancer Cells by Upregulating S100A4.

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Journal:  PLoS One       Date:  2016-01-07       Impact factor: 3.240

  8 in total
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2.  Overexpressed methyltransferase-like 1 (METTL1) increased chemosensitivity of colon cancer cells to cisplatin by regulating miR-149-3p/S100A4/p53 axis.

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  2 in total

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