TY - UNPB
T1 - Cell Competition Driven by Secreted Ligands
T2 - Modeling Liver Metastasis of Colorectal Cancer
AU - Nemati, Hossein
AU - Suijkerbuijk, Saskia Jacoba Elisabeth
AU - de Graaf, Joost
PY - 2025/10/24
Y1 - 2025/10/24
N2 - Cell competition in multicellular organisms has been shown to play a critical role during the development of organisms, cancer progression, and in the establishment and maintenance of tissue homeostasis. Various mechanisms of cell competition have been identified, including active elimination via mechanical forces or induced apoptosis, as well as competition for nutrients and other beneficial factors. A recent experiment demonstrated hallmarks of cell competition, associated with cell cycle dynamics, between liver progenitor cells and colorectal cancer cells [Krotenberg Garcia et al., iScience 27, 109718 (2024)]. However, a mechanistic explanation for this form of competition remains lacking. Here, we present a mean-field model of competition for signaling ligands, coupled with cell cycle dynamics, to provide such an understanding. Our model captures the salient features of the experiment, including population dynamics and cell cycle variations. We demonstrate that secretion of a beneficial factor by cells, coupled with the enhanced uptake efficiency of cancer cells, suffices to reproduce the experimental outcome. Our model, reminiscent of competition for secreted growth factors, provides insight into the minimal level of complexity required to achieve the observed competitive outcome as well as its link to cell cycle dynamics. It can also serve as a general framework for studying biological populations with growth-stage-dependent competition over consumer-produced products.
AB - Cell competition in multicellular organisms has been shown to play a critical role during the development of organisms, cancer progression, and in the establishment and maintenance of tissue homeostasis. Various mechanisms of cell competition have been identified, including active elimination via mechanical forces or induced apoptosis, as well as competition for nutrients and other beneficial factors. A recent experiment demonstrated hallmarks of cell competition, associated with cell cycle dynamics, between liver progenitor cells and colorectal cancer cells [Krotenberg Garcia et al., iScience 27, 109718 (2024)]. However, a mechanistic explanation for this form of competition remains lacking. Here, we present a mean-field model of competition for signaling ligands, coupled with cell cycle dynamics, to provide such an understanding. Our model captures the salient features of the experiment, including population dynamics and cell cycle variations. We demonstrate that secretion of a beneficial factor by cells, coupled with the enhanced uptake efficiency of cancer cells, suffices to reproduce the experimental outcome. Our model, reminiscent of competition for secreted growth factors, provides insight into the minimal level of complexity required to achieve the observed competitive outcome as well as its link to cell cycle dynamics. It can also serve as a general framework for studying biological populations with growth-stage-dependent competition over consumer-produced products.
KW - physics.bio-ph
KW - cond-mat.soft
M3 - Preprint
BT - Cell Competition Driven by Secreted Ligands
PB - arXiv
ER -