Jomnarong Lertsuwan
CX-4945 induces methuosis in cholangiocarcinoma cell lines by a CK2-independent mechanism
Lertsuwan, Jomnarong; Lertsuwan, Kornkamon; Sawasdichai, Anyaporn; Tasnawijitwong, Nathapol; Lee, Ka; Kitchen, Philip; Afford, Simon; Gaston, Kevin; Jayaraman, Padma-Sheela; Satayavivad, Jutamaad
Authors
Kornkamon Lertsuwan
Anyaporn Sawasdichai
Nathapol Tasnawijitwong
Ka Lee
Philip Kitchen
Simon Afford
Professor KEVIN GASTON Kevin.Gaston@nottingham.ac.uk
PROFESSOR OF CANCER STUDIES
Padma-Sheela Jayaraman
Jutamaad Satayavivad
Abstract
Cholangiocarcinoma is a disease with a poor prognosis and increasing incidence and hence there is a pressing unmet clinical need for new adjuvant treatments. Protein kinase CK2 (previously casein kinase II) is a ubiquitously expressed protein kinase that is up-regulated in multiple cancer cell types. The inhibition of CK2 activity using CX-4945 (Silmitasertib) has been proposed as a novel treatment in multiple disease settings including cholangiocarcinoma. Here, we show that CX-4945 inhibited the proliferation of cholangiocarcinoma cell lines in vitro. Moreover, CX-4945 treatment induced the formation of cytosolic vacuoles in cholangiocarcinoma cell lines and other cancer cell lines. The vacuoles contained extracellular fluid and had neutral pH, features characteristic of methuosis. In contrast, simultaneous knockdown of both the α and α′ catalytic subunits of protein kinase CK2 using small interfering RNA (siRNA) had little or no effect on the proliferation of cholangiocarcinoma cell lines and failed to induce the vacuole formation. Surprisingly, low doses of CX-4945 increased the invasive properties of cholangiocarcinoma cells due to an upregulation of matrix metallopeptidase 7 (MMP-7), while the knockdown of CK2 inhibited cell invasion. Our data suggest that CX-4945 inhibits cell proliferation and induces cell death via CK2-independent pathways. Moreover, the increase in cell invasion brought about by CX-4945 treatment suggests that this drug might increase tumor invasion in clinical settings.
Citation
Lertsuwan, J., Lertsuwan, K., Sawasdichai, A., Tasnawijitwong, N., Lee, K., Kitchen, P., Afford, S., Gaston, K., Jayaraman, P.-S., & Satayavivad, J. (2018). CX-4945 induces methuosis in cholangiocarcinoma cell lines by a CK2-independent mechanism. Cancers, 10(9), Article 283. https://doi.org/10.3390/cancers10090283
Journal Article Type | Article |
---|---|
Acceptance Date | Aug 20, 2018 |
Online Publication Date | Aug 23, 2018 |
Publication Date | Aug 23, 2018 |
Deposit Date | Aug 23, 2018 |
Publicly Available Date | Aug 23, 2018 |
Journal | Cancers |
Electronic ISSN | 2072-6694 |
Publisher | MDPI |
Peer Reviewed | Peer Reviewed |
Volume | 10 |
Issue | 9 |
Article Number | 283 |
DOI | https://doi.org/10.3390/cancers10090283 |
Keywords | protein kinase CK2; CX-4945; cholangiocarcinoma; non-canonical cell death; methuosis |
Public URL | https://nottingham-repository.worktribe.com/output/1045216 |
Publisher URL | http://www.mdpi.com/2072-6694/10/9/283 |
Contract Date | Aug 23, 2018 |
Files
Lertsuwan Et Al Cancers 2018
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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