Mechanosensitive calcium channels and integrins coordinate the reprogramming of colorectal cancer cells into a fetal-like state

Colorectal cancer (CRC) cells exhibit high plasticity and transition between different cellular states during the development of metastasis. Lgr5-expressing cancer stem cells fuel the growth of the primary tumor and metastasis, yet disseminated tumor cells arriving at the metastatic site and seeding liver metastases are devoid of Lgr5 expression. Using CRC organoid models, we demonstrate that mechanical interactions with collagen I, a main constituent of the interstitial matrix, instruct the reprogramming of CRC cells. Collagen I-induced pulling forces are sensed by integrins and mechanosensitive calcium channels, which together direct the transition of CRC cells into a cellular state with transcriptional similarities to fetal intestinal cells. CRC cells infiltrating the interstitial stroma show upregulation of this fetal-like transcriptional program, which correlates with the ability of Lgr5-negative cells to initiate metastasis formation. Our findings indicate that mechanical interactions with collagen I regulate cell fate transitions associated with the metastatic cascade of CRC.

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Publication Details

Journal
Cell Reports
Published
2025-09-23
DOI
https://doi.org/10.1016/j.celrep.2025.116308
Citations
3
Primary Topic
Erythrocyte Function and Pathophysiology
Type
article
Field-Weighted Citation Impact
3.49

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article

Mechanosensitive calcium channels and integrins coordinate the reprogramming of colorectal cancer cells into a fetal-like state

Femke Simmer, Ronja M. Houtekamer, Onno Kranenburg, Lars J S Kemp et al.
3 citations
Cell Reports
Erythrocyte Function and Pathophysiology
3.49
article

Mechanosensitive calcium channels and integrins coordinate the reprogramming of colorectal cancer cells into a fetal-like state

Femke Simmer, Ronja M. Houtekamer, Onno Kranenburg, Lars J S Kemp, Marjolein J. Vliem, Susan Zwakenberg, Mirjam C. van der Net, Tariq Sami Haddad, Carlos Pérez‐González, Hugo J.G. Snippert, Esther Strating, Suzanne E. M. van der Horst, Jacco van Rheenen, Antoine Khalil, Danijela Matic Vignjevic, Willem‐Jan Pannekoek, Saskia J.E. Suijkerbuijk, Martijn Gloerich, Jooske L. Monster, Ana Krotenberg-Garcia, Karen B. van den Anker, Iris D. Nagtegaal
article en
3 citations

Abstract

Colorectal cancer (CRC) cells exhibit high plasticity and transition between different cellular states during the development of metastasis. Lgr5-expressing cancer stem cells fuel the growth of the primary tumor and metastasis, yet disseminated tumor cells arriving at the metastatic site and seeding liver metastases are devoid of Lgr5 expression. Using CRC organoid models, we demonstrate that mechanical interactions with collagen I, a main constituent of the interstitial matrix, instruct the reprogramming of CRC cells. Collagen I-induced pulling forces are sensed by integrins and mechanosensitive calcium channels, which together direct the transition of CRC cells into a cellular state with transcriptional similarities to fetal intestinal cells. CRC cells infiltrating the interstitial stroma show upregulation of this fetal-like transcriptional program, which correlates with the ability of Lgr5-negative cells to initiate metastasis formation. Our findings indicate that mechanical interactions with collagen I regulate cell fate transitions associated with the metastatic cascade of CRC.

Cell ReportsVol. 44(10)
Centre National de la Recherche Scientifique (FR), Radboud University Nijmegen (NL), Utrecht University (NL), Université Paris Sciences et Lettres (FR), Radboud University Medical Center (NL), University Medical Center Utrecht (NL), Oncode Institute (NL), Cancer Genomics Centre (NL), Institut Curie (FR)
Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Universitair Medisch Centrum Utrecht
Openalex Percentile: Top 7%
Erythrocyte Function and Pathophysiology
3.49
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