» Articles » PMID: 30445944

A Tight Balance of Karyopherin β1 Expression is Required in Cervical Cancer Cells

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2018 Nov 18
PMID 30445944
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Karyopherin β1 (Kpnβ1) is the main nuclear import protein involved in the transport of cargoes from the cytoplasm into the cell nucleus. Previous research has found Kpnβ1 to be significantly overexpressed in cervical cancer and other cancer tissues, and further studies showed that inhibition of Kpnβ1 expression by siRNA resulted in cancer cell death, while non-cancer cells were minimally affected. These results suggest that Kpnβ1 has potential as an anticancer therapeutic target, thus warranting further research into the association between Kpnβ1 expression and cancer progression. Here, the biological effects associated with Kpnβ1 overexpression were investigated in order to further elucidate the relationship between Kpnβ1 and the cancer phenotype.

Methods: To evaluate the effect of Kpnβ1 overexpression on cell biology, cell proliferation, cell cycle, cell morphology and cell adhesion assays were performed. To determine whether Kpnβ1 overexpression influences cell sensitivity to chemotherapeutic agents like Cisplatin, cell viability assays were performed. Expression levels of key proteins were analysed by Western blot analysis.

Results: Our data revealed that Kpnβ1 overexpression, above that which was already detected in cancer cells, resulted in reduced proliferation of cervical cancer cells. Likewise, normal epithelial cells showed reduced proliferation after Kpnβ1 overxpression. Reduced cancer cell proliferation was associated with a delay in cell cycle progression, as well as changes in the morphology and adhesion properties of cells. Additionally, Kpnβ1 overexpressing HeLa cells exhibited increased sensitivity to cisplatin, as shown by decreased cell viability and increased apoptosis, where p53 and p21 inhibition reduced and enhanced cell sensitivity to Cisplatin, respectively.

Conclusions: Overall, our results suggest that a tight balance of Kpnβ1 expression is required for cellular function, and that perturbation of this balance results in negative effects associated with a variety of biological processes.

Citing Articles

A mass spectrometry-based approach for the identification of Kpnβ1 binding partners in cancer cells.

Okpara M, Hermann C, van der Watt P, Garnett S, Blackburn J, Leaner V Sci Rep. 2022; 12(1):20171.

PMID: 36418423 PMC: 9684564. DOI: 10.1038/s41598-022-24194-6.


Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental validation.

Panagiotopoulos A, Kalyvianaki K, Tsodoulou P, Darivianaki M, Dellis D, Notas G Comput Struct Biotechnol J. 2022; 20:5952-5961.

PMID: 36382187 PMC: 9646746. DOI: 10.1016/j.csbj.2022.10.015.


Expression of Karyopherin Alpha 2 and Karyopherin Beta 1 Correlate with Poor Prognosis in Gastric Cancer.

Ohhara Y, Kinoshita I, Suzuki A, Imagawa M, Taguchi J, Noguchi T Oncology. 2022; 100(12):685-695.

PMID: 36273446 PMC: 9808660. DOI: 10.1159/000526807.


Inhibition of Kpnβ1 mediated nuclear import enhances cisplatin chemosensitivity in cervical cancer.

Chi R, van der Watt P, Wei W, Birrer M, Leaner V BMC Cancer. 2021; 21(1):106.

PMID: 33530952 PMC: 7852134. DOI: 10.1186/s12885-021-07819-3.


Inhibiting Importin 4-mediated nuclear import of CEBPD enhances chemosensitivity by repression of PRKDC-driven DNA damage repair in cervical cancer.

Zhou Y, Liu F, Xu Q, Yang B, Li X, Jiang S Oncogene. 2020; 39(34):5633-5648.

PMID: 32661323 PMC: 7441007. DOI: 10.1038/s41388-020-1384-3.

References
1.
Ciciarello M, Mangiacasale R, Thibier C, Guarguaglini G, Marchetti E, Di Fiore B . Importin beta is transported to spindle poles during mitosis and regulates Ran-dependent spindle assembly factors in mammalian cells. J Cell Sci. 2004; 117(Pt 26):6511-22. DOI: 10.1242/jcs.01569. View

2.
Larue L, Bellacosa A . Epithelial-mesenchymal transition in development and cancer: role of phosphatidylinositol 3' kinase/AKT pathways. Oncogene. 2005; 24(50):7443-54. DOI: 10.1038/sj.onc.1209091. View

3.
Maritz M, van der Watt P, Holderness N, Birrer M, Leaner V . Inhibition of AP-1 suppresses cervical cancer cell proliferation and is associated with p21 expression. Biol Chem. 2011; 392(5):439-48. DOI: 10.1515/BC.2011.036. View

4.
van der Watt P, Maske C, Hendricks D, Parker M, Denny L, Govender D . The Karyopherin proteins, Crm1 and Karyopherin beta1, are overexpressed in cervical cancer and are critical for cancer cell survival and proliferation. Int J Cancer. 2009; 124(8):1829-40. PMC: 6944291. DOI: 10.1002/ijc.24146. View

5.
Azmi A . Unveiling the role of nuclear transport in epithelial-to-mesenchymal transition. Curr Cancer Drug Targets. 2013; 13(9):906-14. DOI: 10.2174/15680096113136660096. View