Evidence map›Paper›PMID 40809136›Full record

ArticleFrontiers in systems biology2024

Integrating inverse reinforcement learning into data-driven mechanistic computational models: a novel paradigm to decode cancer cell heterogeneity.

Patrick C Kinnunen, Kenneth K Y Ho, Siddhartha Srivastava, Chengyang Huang, Wanggang Shen, Krishna Garikipati, Gary D Luker, Nikola Banovic, Xun Huan, Jennifer J Linderman and 1 more

Abstract read
In one paragraph

Article in Frontiers in systems biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Patrick C KinnunenDepartments of Chemical Engineering, University of Michigan, Ann Arbor, MI, United States.
Kenneth K Y HoRadiology, University of Michigan, Ann Arbor, MI, United States.
Siddhartha SrivastavaMechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Chengyang HuangMechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Wanggang ShenMechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Krishna GarikipatiMechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Gary D LukerRadiology, University of Michigan, Ann Arbor, MI, United States.
Nikola BanovicElectrical Engineering and Computer Science, University of Michigan, Ann Arbor, MI, United States.
Xun HuanMechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Jennifer J LindermanDepartments of Chemical Engineering, University of Michigan, Ann Arbor, MI, United States.
Kathryn E LukerRadiology, University of Michigan, Ann Arbor, MI, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular heterogeneity is a ubiquitous aspect of biology and a major obstacle to successful cancer treatment. Several techniques have emerged to quantify heterogeneity in live cells along axes including cellular migration, morphology, growth, and signaling. Crucially, these studies reveal that cellular heterogeneity is not a result of randomness or a failure in cellular control systems, but instead is a predictable aspect of multicellular systems. We hypothesize that individual cells in complex tissues can behave as reward-maximizing agents and that differences in reward perception can explain heterogeneity. In this perspective, we introduce inverse reinforcement learning as a novel approach for analyzing cellular heterogeneity. We briefly detail experimental approaches for measuring cellular heterogeneity over time and how these experiments can generate datasets consisting of cellular states and actions. Next, we show how inverse reinforcement learning can be applied to these datasets to infer how individual cells choose different actions based on heterogeneous states. Finally, we introduce potential applications of inverse reinforcement learning to three cell biology problems. Overall, we expect inverse reinforcement learning to reveal why cells behave heterogeneously and enable identification of novel treatments based on this new understanding.

Indexed as

cellular heterogeneityinverse reinforcment learninglive-cell microscopymachine learningmechanistic modeling

Identifiers

PMID40809136
PMCPMC12342033

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.