La Trobe

Combination of bazedoxifene with chemotherapy and SMAC-mimetics for the treatment of colorectal cancer

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posted on 2024-04-18, 04:57 authored by Rhynelle Sidney DmelloRhynelle Sidney Dmello, Michelle Palmieri, Pathum S Thilakasiri, Larissa Doughty, Tracy L Nero, Ashleigh PohAshleigh Poh, Sarah Q To, Erinna LeeErinna Lee, Walter FairlieWalter Fairlie, Lisa MielkeLisa Mielke, Michael W Parker, Ivan PoonIvan Poon, Eduard Batlle, Matthias ErnstMatthias Ernst, Ashwini ChandAshwini Chand
Excessive STAT3 signalling via gp130, the shared receptor subunit for IL-6 and IL-11, contributes to disease progression and poor survival outcomes in patients with colorectal cancer. Here, we provide evidence that bazedoxifene inhibits tumour growth via direct interaction with the gp130 receptor to suppress IL-6 and IL-11-mediated STAT3 signalling. Additionally, bazedoxifene combined with chemotherapy synergistically reduced cell proliferation and induced apoptosis in patient-derived colon cancer organoids. We elucidated that the primary mechanism of anti-tumour activity conferred by bazedoxifene treatment occurs via pro-apoptotic responses in tumour cells. Co-treatment with bazedoxifene and the SMAC-mimetics, LCL161 or Birinapant, that target the IAP family of proteins, demonstrated increased apoptosis and reduced proliferation in colorectal cancer cells. Our findings provide evidence that bazedoxifene treatment could be combined with SMAC-mimetics and chemotherapy to enhance tumour cell apoptosis in colorectal cancer, where gp130 receptor signalling promotes tumour growth and progression.

Funding

The study was supported by the following grants and fellowship schemes: Victorian Cancer Agency (19014 and MCRF19045), Cancer Council Victoria (1143036), National Health and Medical Research Council (NHMRC) support of MWP (Leadership Fellow, 1194263), ARP (Peter Doherty Early Career Research Fellow, 1166447) and ME (Principal Research Fellow). RSD is supported by La Trobe University Full-Fee Research Scholarship and La Trobe University Postgraduate Research Scholarship. NHMRC Independent Research Institutes Infrastructure Support Scheme to SVI is acknowledged. Funding from the Perpetual Trust Impact Grant is acknowledged. Institutional funding from the Victorian State Government Operational Infrastructure Support Scheme to SVI, ONJCRI and Ludwig Cancer Research is acknowledged. We acknowledge the Australian Cancer Research Foundation (ACRF) and The Collie Foundation for providing funds to purchase the Zeiss 980 confocal microscope.

History

Publication Date

2024-04-10

Journal

Cell Death and Disease

Volume

15

Article Number

255

Pagination

13p.

Publisher

Springer Nature

ISSN

2041-4889

Rights Statement

© The Author(s) 2024 This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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