» Articles » PMID: 18356295

Closed-loop Control of Cellular Functions Using Combinatory Drugs Guided by a Stochastic Search Algorithm

Overview
Specialty Science
Date 2008 Mar 22
PMID 18356295
Citations 83
Authors
Affiliations
Soon will be listed here.
Abstract

A mixture of drugs is often more effective than using a single effector. However, it is extremely challenging to identify potent drug combinations by trial and error because of the large number of possible combinations and the inherent complexity of the underlying biological network. With a closed-loop optimization modality, we experimentally demonstrate effective searching for potent drug combinations for controlling cellular functions through a large parametric space. Only tens of iterations out of one hundred thousand possible trials were needed to determine a potent combination of drugs for inhibiting vesicular stomatitis virus infection of NIH 3T3 fibroblasts. In addition, the drug combination reduced the required dosage by approximately 10-fold compared with individual drugs. In another example, a potent mixture was identified in thirty iterations out of a possible million combinations of six cytokines that regulate the activity of nuclear factor kappa B in 293T cells. The closed-loop optimization approach possesses the potential of being an effective approach for manipulating a wide class of biological systems.

Citing Articles

Flash optimization of drug combinations for Acinetobacter baumannii with IDentif.AI-AMR.

You K, Binte Mohamed Yazid N, Chong L, Hooi L, Wang P, Zhuang I NPJ Antimicrob Resist. 2025; 3(1):12.

PMID: 39984645 PMC: 11845484. DOI: 10.1038/s44259-025-00079-2.


Radiation therapy with phenotypic medicine: towards N-of-1 personalization.

Chong L, Wang P, Lee V, Vijayakumar S, Tan H, Wang F Br J Cancer. 2024; 131(1):1-10.

PMID: 38514762 PMC: 11231338. DOI: 10.1038/s41416-024-02653-3.


CURATE.AI COR-Tx platform as a digital therapy and digital diagnostic for cognitive function in patients with brain tumour postradiotherapy treatment: protocol for a prospective mixed-methods feasibility clinical trial.

Remus A, Tadeo X, Kai G, Blasiak A, Kee T, Vijayakumar S BMJ Open. 2023; 13(10):e077219.

PMID: 37879700 PMC: 10603439. DOI: 10.1136/bmjopen-2023-077219.


Review of Predicting Synergistic Drug Combinations.

Pan Y, Ren H, Lan L, Li Y, Huang T Life (Basel). 2023; 13(9).

PMID: 37763281 PMC: 10533134. DOI: 10.3390/life13091878.


Uncovering expression signatures of synergistic drug responses via ensembles of explainable machine-learning models.

Janizek J, Dincer A, Celik S, Chen H, Chen W, Naxerova K Nat Biomed Eng. 2023; 7(6):811-829.

PMID: 37127711 PMC: 11149694. DOI: 10.1038/s41551-023-01034-0.


References
1.
Siebenlist U, Franzoso G, Brown K . Structure, regulation and function of NF-kappa B. Annu Rev Cell Biol. 1994; 10:405-55. DOI: 10.1146/annurev.cb.10.110194.002201. View

2.
Li X, Zhao X, Fang Y, Jiang X, Duong T, Fan C . Generation of destabilized green fluorescent protein as a transcription reporter. J Biol Chem. 1998; 273(52):34970-5. DOI: 10.1074/jbc.273.52.34970. View

3.
Blakey G, Lockton J, Perrett J, Norwood P, Russell M, Aherne Z . Pharmacokinetic and pharmacodynamic assessment of a five-probe metabolic cocktail for CYPs 1A2, 3A4, 2C9, 2D6 and 2E1. Br J Clin Pharmacol. 2004; 57(2):162-9. PMC: 1884443. DOI: 10.1046/j.1365-2125.2003.01973.x. View

4.
Banan A, Farhadi A, Fields J, Mutlu E, Zhang L, Keshavarzian A . Evidence that nuclear factor-kappa B activation is critical in oxidant-induced disruption of the microtubule cytoskeleton and barrier integrity and that its inactivation is essential in epidermal growth factor-mediated protection of the monolayers.... J Pharmacol Exp Ther. 2003; 306(1):13-28. DOI: 10.1124/jpet.103.047415. View

5.
Nakanishi C, Toi M . Nuclear factor-kappaB inhibitors as sensitizers to anticancer drugs. Nat Rev Cancer. 2005; 5(4):297-309. DOI: 10.1038/nrc1588. View