open access

Vol 53, No 1 (2015)
Original paper
Submitted: 2015-03-18
Accepted: 2015-03-20
Published online: 2015-04-14
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The alterations in SATB1 and nuclear F-actin expression affect apoptotic response of the MCF-7 cells to geldanamycin

Dariusz Grzanka, Magdalena Izdebska, Anna Klimaszewska-Wisniewska, Maciej Gagat
DOI: 10.5603/FHC.a2015.0008
·
Pubmed: 25809470
·
Folia Histochem Cytobiol 2015;53(1):79-87.

open access

Vol 53, No 1 (2015)
ORIGINAL PAPERS
Submitted: 2015-03-18
Accepted: 2015-03-20
Published online: 2015-04-14

Abstract

Introduction. The function and localization of actin in the nucleus have not yet been fully described. However, actin seems to be a key protein in nuclear processes interacting with chromatin and matrix proteins. The aim of the study was to evaluate the effect of controlled expression of nuclear pool of F-actin and special AT-rich sequence-binding protein 1 (SATB1) on the in vitro induction of active cell death by geldanamycin (GA).

Material and methods. The expression of SATB1 was regulated by the transfection of non-aggressive breast cancer MCF-7 cells with siRNA against SATB1 or expression plasmid with cloned cDNA of SATB1. The altered expression of cofilin-1 in these cells was used to regulate the nuclear expression and localization of F-actin. The effect of GA was analyzed in the context of cell death induction and cell cycle alterations.

Results. Our studies revealed that the targeted regulation of SATB1 and cofilin-1 expression changed the apoptotic response of the MCF-7 cells to GA. The overexpression of these proteins potentiated GA-induced arrest of the cells in the G1 phase of cell cycle and increased the population of the hypodiploid cells.

Conclusion. The alterations in the nuclear expression of SATB1 and F-actin in MCF-7 cells may affect their active cell death in response to GA.

Abstract

Introduction. The function and localization of actin in the nucleus have not yet been fully described. However, actin seems to be a key protein in nuclear processes interacting with chromatin and matrix proteins. The aim of the study was to evaluate the effect of controlled expression of nuclear pool of F-actin and special AT-rich sequence-binding protein 1 (SATB1) on the in vitro induction of active cell death by geldanamycin (GA).

Material and methods. The expression of SATB1 was regulated by the transfection of non-aggressive breast cancer MCF-7 cells with siRNA against SATB1 or expression plasmid with cloned cDNA of SATB1. The altered expression of cofilin-1 in these cells was used to regulate the nuclear expression and localization of F-actin. The effect of GA was analyzed in the context of cell death induction and cell cycle alterations.

Results. Our studies revealed that the targeted regulation of SATB1 and cofilin-1 expression changed the apoptotic response of the MCF-7 cells to GA. The overexpression of these proteins potentiated GA-induced arrest of the cells in the G1 phase of cell cycle and increased the population of the hypodiploid cells.

Conclusion. The alterations in the nuclear expression of SATB1 and F-actin in MCF-7 cells may affect their active cell death in response to GA.

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Keywords

SATB1; F-actin; cofilin-1; geldanamycin; apoptosis; MCF-7 cells; siRNA; transfection

About this article
Title

The alterations in SATB1 and nuclear F-actin expression affect apoptotic response of the MCF-7 cells to geldanamycin

Journal

Folia Histochemica et Cytobiologica

Issue

Vol 53, No 1 (2015)

Article type

Original paper

Pages

79-87

Published online

2015-04-14

Page views

1953

Article views/downloads

2178

DOI

10.5603/FHC.a2015.0008

Pubmed

25809470

Bibliographic record

Folia Histochem Cytobiol 2015;53(1):79-87.

Keywords

SATB1
F-actin
cofilin-1
geldanamycin
apoptosis
MCF-7 cells
siRNA
transfection

Authors

Dariusz Grzanka
Magdalena Izdebska
Anna Klimaszewska-Wisniewska
Maciej Gagat

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