Artificial Intelligence-Driven Natural Product Discovery for Cancer Metastasis and Chemoresistance: From Computational Prediction to Preclinical Validation

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Authors: Mohamed Ali Hussein, Gnanasekar Munirathinam
Cited by: 3
References: 206

Abstract

Cancer metastasis and chemoresistance are primary reasons for cancer-related mortality. Current therapeutic options rely mostly on single-target drugs, which often fail to exhibit long-lasting remission of the disease progression due to the complexity of metastasis and resistance mechanisms. Natural products (NPs) possess inherent structural diversity, rendering them suitable as multi-target agents. The utilization of NPs is often impeded in treating complex diseases such as cancer, even though approximately 65% of approved anticancer drugs are NP derivatives, or synthetic derivatives containing NP-pharmacophores, due to various factors, including poor aqueous solubility and variable oral bioavailability, structural complexity, synthetic inaccessibility, and stereochemical diversity that confounds structure-activity relationship analyses. This review discusses how integrating artificial intelligence (AI) and machine learning (ML) with chemoinformatics can identify, prioritize, and experimentally validate NPs, potentially paving the way for new drugs that address intricate processes such as metastasis and resistance. We summarize the recent computational advances in the field, including graph neural networks, attention mechanisms, Siamese networks, virtual screening, and network pharmacology. These advancements address ADMET optimization, molecular representation, virtual screening, network pharmacology, and experimental validation. We emphasize how each of these approaches tackles the unique challenges associated with NPs. We contextualize our review within the specific challenges presented by the chemical space of NPs. Additionally, we analyze real-world case studies of successful AI-assisted NP discovery and categorize the quality of evidence into three levels: Level A, which includes in vivo efficacy with mechanistic details; Level B, which consists of in vitro validation of mechanisms and phenotypes; and Level C, which represents computational hypotheses that are awaiting experimental verification. Additionally, we propose an operational framework for selecting suitable AI methodologies based on available data, target characterization, and validation resources. Finally, we emphasize the limitations and future directions in AI-facilitated NP discovery.

Fields of Study & Subjects

Computational Drug Discovery Methods Microbial Natural Products and Biosynthesis Histone Deacetylase Inhibitors Research

Publication details

Journal / source
Cancers
Publisher
MDPI AG
Volume
18
Issue
5
Pages
719–719
Publication date
24 February 2026
Language
EN