Evidence map›Paper›PMID 38802748›Full record

ArticleBMC bioinformatics2024

LinG3D: visualizing the spatio-temporal dynamics of clonal evolution.

Anjun Hu, Awino Maureiq E Ojwang', Kayode D Olumoyin, Katarzyna A Rejniak

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Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Anjun Hu *Integrated Mathematical Oncology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA.
Awino Maureiq E Ojwang' *Integrated Mathematical Oncology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA.
Kayode D Olumoyin *Integrated Mathematical Oncology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA.
Katarzyna A RejniakIntegrated Mathematical Oncology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA. kasia.rejniak@moffitt.org.

Funding

Ecology and Evolution of Breast CarcinogenesisU01CA261841 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI DAMAGHI, MEHDI, SIQUEIRA SILVA, ARIOSTO S · 2021 to 2025
$3.0M
Modeling the role and regulation of reactive stroma in breast ductal carcinoma microinvasionsR01CA272601 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI DAMAGHI, MEHDI, REJNIAK, KATARZYNA ANNA · 2022 to 2025
$2.9M
Mathematical Model-Guided Adoptive Immunotherapy in Bladder CancerR01CA259387 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI PILON-THOMAS, SHARI, REJNIAK, KATARZYNA ANNA · 2021 to 2025
$2.3M
NCI NIH HHS R01 CA259387NCI NIH HHS R01 CA272601NCI NIH HHS U01 CA261841NIH HHS CA272601
6 · The paper itself

Abstract

backgroundCancers are spatially heterogenous, thus their clonal evolution, especially following anti-cancer treatments, depends on where the mutated cells are located within the tumor tissue. For example, cells exposed to different concentrations of drugs, such as cells located near the vessels in contrast to those residing far from the vasculature, can undergo a different evolutionary path. However, classical representations of cell lineage trees do not account for this spatial component of emerging cancer clones. Here, we propose routines to trace spatial and temporal clonal evolution in computer simulations of the tumor evolution models.

resultsThe LinG3D (Lineage Graphs in 3D) is an open-source collection of routines (in MATLAB, Python, and R) that enables spatio-temporal visualization of clonal evolution in a two-dimensional tumor slice from computer simulations of the tumor evolution models. These routines draw traces of tumor clones in both time and space, and may include a projection of a selected microenvironmental factor, such as the drug or oxygen distribution within the tumor, if such a microenvironmental factor is used in the tumor evolution model. The utility of LinG3D has been demonstrated through examples of simulated tumors with different number of clones and, additionally, in experimental colony growth assay.

conclusionsThis routine package extends the classical lineage trees, that show cellular clone relationships in time, by adding the space component to show the locations of cellular clones within the 2D tumor tissue patch from computer simulations of tumor evolution models.

Indexed as

Clonal EvolutionNeoplasmsComputer SimulationHumansSoftware3D visualizationLineage treesMathematical modeling of tumor evolutionSpatial clone distribution

Identifiers

PMID38802748
PMCPMC11131251

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