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DOI 10.1007/s12094-017-1633-2

Медицинская библиотека · Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2017

BRG1 regulation by miR-155 in human leukemia and lymphoma cell lines.

Cuadros M, Sánchez-Martín V, Herrera A, Baliñas C, Martín-Padrón J, Boyero L, Peinado P, Medina P P

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Аннотация

INTRODUCTION/PURPOSE: BRG1 is a key regulator of leukemia stem cells. Indeed, it has been observed that this type of cells is unable to divide, survive and develop new tumors when BRG1 is down-regulated.

MATERIALS AND

METHODS

We assessed BRG1 and miR-155 expression in 23 leukemia cell lines, and two no pathological lymphocyte samples using qPCR. MiR-155 transfection and western blot were used to analyze the relationship between miR-155 and its validated target, BRG1, by measuring protein expression levels. The effect of miR-155 on cell proliferation and prednisolone sensitivity were studied with resazurin assay.

RESULTS

BRG1 expression levels could correlate negatively with miR-155 expression levels, at least in Burkitt's lymphoma and diffuse large B cell lymphoma (DLBCL) cell lines. To clarify the role of miR-155 in the regulation of BRG1 expression, we administrated miR-155 mimics in different leukemia/lymphoma cell lines. Our results suggest that miR-155 regulate negatively and significantly the BRG1 expression at least in the MOLT4 cell line.

CONCLUSION

Our study revealed a previously unknown miR-155 heterogeneity that could result in differences in the treatment with miRNAs in our attempt to inhibit BRG1. However, the expression levels of BRG1 and miR-155, before prednisolone treatment were not statistically significantly associated prednisolone sensitive leukemia cells.

Для цитирования: Cuadros M, Sánchez-Martín V, Herrera A, Baliñas C, Martín-Padrón J, Boyero L, Peinado P, Medina P P. BRG1 regulation by miR-155 in human leukemia and lymphoma cell lines.. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico. 2017. DOI: 10.1007/s12094-017-1633-2.

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