Evidence map›Paper›PMID 42779758›Full record

ArticlebioRxiv : the preprint server for biology2026

How optimal control of cellular cost shapes population-level tumor growth dynamics.

Pujan Shrestha, Jason T George

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Pujan ShresthaDepartment of Biomedical Engineering, College Station, TX 77843.ORCID 0000-0002-6301-0383
Jason T GeorgeDepartment of Biomedical Engineering, College Station, TX 77843.ORCID 0000-0002-8248-2888

Funding

Quantifying phenotypic adaptation of biological systems in dynamic environmentsR35GM155458 · NIGMS · TEXAS ENGINEERING EXPERIMENT STATION · PI Jason George · 2024 to 2026
$1.1M
NIGMS NIH HHS R35 GM155458
6 · The paper itself

Abstract

Tumor progression is often modeled as a passive response to external therapy or immune pressure, but tumor populations may also exhibit population-level regulation of proliferation and apoptosis. We develop a continuous-time Markov decision framework in which a controlled birth-death process represents a tumor population modulating the balance between proliferation and susceptibility to apoptosis in the presence of extrinsic death pressure. We examine threshold and quadratic costs, an unbounded linear reward, and constrained linear and quadratic formulations to determine how objective structure shapes optimal policies and induced population drift. Threshold and quadratic penalties generate restoring dynamics, with transitions from growth to suppression and regions of near-neutral drift associated with regulated or near-dormant behavior. An unbounded linear reward instead produces sustained or near-neutral growth without a restoring regime. Under constraints, a linear reward expands the region of positive drift as capacity increases, whereas a quadratic reward can generate restoring, logistic-like drift around an interior population scale. These results show that regulated tumor dynamics depend on how growth incentives, extrinsic death pressure, penalties, and constraints scale with population size.

Indexed as

Cancer dynamicsContinuous-time Markov decision processesMathematical oncologyOptimal controlTumor dormancy

Identifiers

PMID42779758
PMCPMC13596463

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.