ArticleJournal of mathematical biology2024
Tumor growth and population modeling in a toxicant-stressed random environment.
Article in Journal of mathematical biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Article
- Stochastic modeling and first-passage-time analysis of oncological time metrics with dynamic tumor barriers.Scientific reports · 2025Article
Corrections and comments
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Authors and funding
1 author.
Funding
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Abstract
When examining some factors that contribute to the growth or decline of a population or tumor, it is essential to consider a random hypothesis. By analyzing the effects of stress on a population (or volume of tumor growth) in a random environment, we develop stochastic models describing the dynamics of the population (or tumor growth) based on random adjustments to the population's intrinsic growth rate, carrying capacity, and harvesting efforts (or tumor treatments). Apart from the models' ability to capture fluctuations, the availability of a shape parameter in the models gives it the flexibility to describe a variety of population/tumor data with different shapes. The distribution of the stressed population size with or without harvesting (or treatments) is derived and used to calculate the maximum expected amount of harvests that can be taken from the population without depleting resources in the long run (or the minimum amount of chemotherapy needed to cause shrinkage or eradication of a tumor). The work done is applied to analyze tumor growth using published data comprising of the volume of breast tumor obtained by orthotopically implanting LM2-[Formula: see text] cells into the right inguinal mammary fat pads of 6- to 8-week-old female Severe Combined Immuno-Deficient mice.
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Registered trials
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