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Drug combination therapy against cancer has been a promising approach in precision oncology. In recent literature, most anticancer drug combinations (ADC) are estimated and derived from their independent drug response efficacy. Synergistic drug combination response is the most effective drug therapy for various cancer treatments. However, the ADC identification problem is challenging and practically infeasible to exhaustively screen out experimentally from the extensive ADCs. Therefore, computational approaches can be efficiently used to measure and identify drug combination responses in precision oncology. In recent decades, numerous computational approaches have been applied and proposed to predict the responses of clinical ADC using different pharmacological and multi-omics cancer data. Effective computational tools and approaches are needed to predict and measure ADC, address its challenges, and reduce complexity. We have reviewed state-of-the-art computational methods for ADC prediction in the recent decade. This review paper has provided an overview of synergistic ADC response and computational machine-learning approaches for ADC. A critical discussion of the advantages and limitations is also provided. Moreover, we have reviewed the recent existing drug combination resources for ADC response prediction and found the most influential computational method for anticancer drug combination response. Finally, we have compared different computational approaches using benchmark data for ADC responses and discussed the experimental results, limitations, and future direction of ADC responses in precision oncology.
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http://dx.doi.org/10.1016/j.compbiomed.2025.110788 | DOI Listing |
Braz J Biol
September 2025
Universidade Estadual Paulista (Unesp), Instituto de Ciência e Tecnologia, Departamento de Engenharia Ambiental, São José dos Campos, SP, Brasil.
The present study carried out the first systematic review with meta-analysis on the effects of metals and temperature rise individually and their associations with terrestrial invertebrates. Initially, a systematic review of peer-reviewed articles was performed. Meta-analysis demonstrated that metals negatively affected the fitness of annelids, arthropods, and nematodes and positively affected physiological regulation in annelids.
View Article and Find Full Text PDFMem Inst Oswaldo Cruz
September 2025
Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório Interdisciplinar de Pesquisas Médicas, Rio de Janeiro, RJ, Brasil.
Background: Parasite antigens and plasma lipopolysaccharide (LPS) levels from luminal origin in visceral leishmaniasis (VL) patients are correlated with cellular activation and low CD4+T cell counts.
Objectives: Our aim was to verify whether Leishmania infantum infection damages the intestinal barrier and whether combination antimonial/antibiotic contributes to the reduction of LPS levels and immune activation.
Methods: Golden hamsters were grouped in: G1-uninfected; G2-infected with L.
Braz Oral Res
September 2025
Universidade de São Paulo - USP, Bauru School of Dentistry, Department of Pediatric Dentistry, Orthodontics and Public Health, Bauru, SP, Brazil.
This in vitro study evaluated the effect of proanthocyanidin, palm oil, and vitamin E against initial erosion. Bovine enamel blocks (n = 140) were divided into 14 groups: C+_SnCl2/NaF/Am-F-containing solution (positive control); C-_deionized water (negative control); O_palm oil; P6.5_6.
View Article and Find Full Text PDFSci Adv
September 2025
Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
(phosphatidylserine synthase 1) encodes an enzyme that facilitates production of phosphatidylserine (PS), which mediates a global immunosuppressive signal. Here, based on in vivo CRISPR screen, we identified PTDSS1 as a target to improve anti-PD-1 therapy. Depletion of in tumor cells increased expression of interferon-γ (IFN-γ)-regulated genes, including , , , and , even in the absence of IFN-γ stimulation in vitro.
View Article and Find Full Text PDFPLoS Comput Biol
September 2025
Systems Biology and Bioinformatics, Case Western Reserve University School of Medicine, Cleveland, Ohio, United States of America.
Gene signatures predictive of chemotherapeutic response have the potential to extend the reach of precision medicine by allowing oncologists to optimize treatment for individuals. Most published predictive signatures are only capable of predicting response for individual drugs, but most chemotherapy regimens utilize combinations of different agents. We propose a unified framework, called the chemogram, that uses predictive signatures to rank the relative predicted sensitivity of different drugs for individual tumors.
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