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Targeting the Nuclear Import Receptor Kpnβ1 as an Anticancer Therapeutic
Pauline J van der Watt1, Alicia Chi1, Tamara Stelma1
1Division of Medical Biochemistry, Department of Integrative Biomedical Sciences, Institute of Infectious Disease and Molecular Medicine, SAMRC/UCT Gynaecological Cancer Research Centre, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Abstract:
Karyopherin beta 1 (Kpnβ1) is a nuclear transport receptor that imports cargoes into the nucleus. Recently, elevated Kpnβ1 expression was found in certain cancers and Kpnβ1 silencing with siRNA was shown to induce cancer cell death. This study aimed to identify novel small molecule inhibitors of Kpnβ1, and determine their anticancer activity. An in silico screen identified molecules that potentially bind Kpnβ1 and Inhibitor of Nuclear Import-43, INI-43 (3-(1H-benzimidazol-2-yl)-1-(3-dimethylaminopropyl)pyrrolo[5,4-b]quinoxalin-2-amine) was investigated further as it interfered with the nuclear localization of Kpnβ1 and known Kpnβ1 cargoes NFAT, NFκB, AP-1, and NFY and inhibited the proliferation of cancer cells of different tissue origins. Minimum effect on the proliferation of noncancer cells was observed at the concentration of INI-43 that showed a significant cytotoxic effect on various cervical and esophageal cancer cell lines. A rescue experiment confirmed that INI-43 exerted its cell killing effects, in part, by targeting Kpnβ1. INI-43 treatment elicited a G2-M cell-cycle arrest in cancer cells and induced the intrinsic apoptotic pathway. Intraperitoneal administration of INI-43 significantly inhibited the growth of subcutaneously xenografted esophageal and cervical tumor cells. We propose that Kpnβ1 inhibitors could have therapeutic potential for the treatment of cancer. Mol Cancer Ther; 15(4); 560-73. ©2016 AACR.
Insights
Novel small molecule INI-43 targets Karyopherin beta 1 (Kpnβ1), a nuclear transport receptor, to inhibit cancer cell proliferation and tumor growth. This Kpnβ1 inhibitor shows therapeutic potential for cancer treatment.
Area of Science:
- Molecular Biology
- Cancer Research
- Drug Discovery
Background:
- Karyopherin beta 1 (Kpnβ1) is a nuclear transport receptor.
- Elevated Kpnβ1 expression is observed in certain cancers.
- Kpnβ1 silencing induces cancer cell death.
Purpose of the Study:
- Identify novel small molecule inhibitors of Kpnβ1.
- Evaluate the anticancer activity of these inhibitors.
- Investigate the therapeutic potential of Kpnβ1 inhibition in cancer.
Main Methods:
- In silico screening to identify potential Kpnβ1 binders.
- In vitro assays using cancer cell lines (cervical, esophageal) and non-cancer cells.
- Rescue experiments to confirm target engagement.
- Cell cycle analysis and apoptosis assays.
- In vivo studies using xenograft tumor models.
Main Results:
- INI-43 identified as a potent Kpnβ1 inhibitor.
- INI-43 interfered with nuclear localization of Kpnβ1 and its cargoes (NFAT, NFκB, AP-1, NFY).
- INI-43 inhibited proliferation of various cancer cells with minimal effect on non-cancer cells.
- INI-43 induced G2-M cell-cycle arrest and apoptosis in cancer cells.
- INI-43 significantly inhibited tumor growth in vivo.
Conclusions:
- Kpnβ1 is a viable therapeutic target for cancer treatment.
- INI-43 demonstrates significant anticancer activity through Kpnβ1 inhibition.
- Small molecule Kpnβ1 inhibitors hold promise for cancer therapy.
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