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EDITORIAL article

Front. Oncol.

Sec. Cancer Metabolism

Volume 15 - 2025 | doi: 10.3389/fonc.2025.1575563

This article is part of the Research Topic Targeting and Monitoring Cancer Metabolism: Novel Theranostics for Colorectal Cancer View all 6 articles

Editorial: Targeting and Monitoring Cancer Metabolism: Novel Theranostics for

Provisionally accepted
  • 1 Department of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan
  • 2 Institute of Quantum Life Science, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan
  • 3 Nagoya City University Hospital, Nagoya, Aichi, Japan

The final, formatted version of the article will be published soon.

    Introduction: Colorectal cancer (CRC) remains a major global health burden, with an increasing emphasis on understanding its metabolic landscape and identifying novel theranostic approaches. In recent years, hyperpolarized 13C-MRI, an innovative imaging technology that visualizes the metabolic characteristics of cancer tissue and metabolic changes induced by treatment, has been developed, leading to a surge in research reports on its applications. The advancement of scientific and technological approaches to understanding cancer metabolism has been remarkable, highlighting the rapid progress in this field. This Research Topic explores how cancer metabolism can be both targeted for therapy and monitored for disease progression, advancing the field of personalized oncology. The five articles published within this topic collectively provide significant contributions to the understanding of metabolic reprogramming in CRC and its potential applications in clinical practice.The first article, Multi-omics analyses of glucose metabolic reprogramming in colorectal cancer (Huang et al., 2023), presents a comprehensive multi-omics approach to dissect the metabolic pathways underlying CRC progression. This study highlights how glucose metabolic reprogramming (GMR) is intricately linked with epithelial-mesenchymal transition (EMT) and metastatic potential. By integrating genomics, proteomics, and metabolomics data, the authors identify novel metabolic markers and propose the CEA/blood glucose ratio as a potential diagnostic tool for CRC liver metastasis.The second article, Development and validation of a risk prediction model for sarcopenia in patients with colorectal cancer (Zhang and Zhu, 2023), addresses the often-overlooked issue of sarcopenia in CRC patients. By constructing a predictive nomogram based on clinical and metabolic parameters, the study offers a valuable tool for early identification of high-risk patients, enabling timely nutritional and therapeutic interventions to improve patient outcomes.The third article, Can proline dehydrogenase-a key enzyme involved in proline metabolism-be a novel target for cancer therapy? (Xu et al., 2023), explores the dual role of proline dehydrogenase (PRODH) in cancer metabolism. While PRODH can induce apoptosis through reactive oxygen species (ROS) signaling, it also promotes tumor survival under hypoxic conditions. This review provides an in-depth discussion on the potential of targeting PRODH as a novel therapeutic strategy for CRC.The fourth article, Fer governs mTORC1 regulating pathways and sustains viability of pancreatic ductal adenocarcinoma cells (Schrier et al., 2024), investigates the regulatory role of the tyrosine kinase Fer in metabolic signaling pathways. Although the study primarily focuses on pancreatic ductal adenocarcinoma, its findings have broader implications for CRC. The study highlights how Fer-mediated regulation of mTORC1 activity influences cellular metabolism, paving the way for potential crosscancer therapeutic applications.The final article, The use of nutrigenomics and nutritional biomarkers with standard care of long-term recurrent metastatic rectal cancer: a case report (Brinkman et al., 2024), presents a compelling case study demonstrating the role of personalized nutrition in CRC management. By integrating nutrigenomics and monitoring key biomarkers such as folate, vitamin B12, and vitamin D, the study underscores the importance of a multidisciplinary approach to improving long-term patient survival.Collectively, these articles underscore the evolving landscape of CRC research, emphasizing metabolic targeting and theranostics as essential components of personalized cancer treatment. From fundamental metabolic pathways to clinical applications, this Research Topic provides a foundation for future studies aimed at optimizing therapeutic strategies for CRC.Regrettably, while this collection provides numerous valuable discussions and insights, it does not include a dedicated discourse on the application of hyperpolarized 13C-MRI. The imaging technology represents a crucial element in the development of new cancer therapies, and further exploration is required to fully realize its potential applications. We look forward to future submissions that introduce novel imaging techniques and fresh perspectives on this technology.We extend our sincere appreciation to all contributing authors, reviewers, and researchers who played a pivotal role in the development of this Research Topic. Their dedication and expertise have made it possible to advance the discourse in oncology, and we look forward to seeing how these findings inspire new research endeavors.I express my gratitude to all contributors who have enriched this theme with their expertise and insights. Finally, I would like to thank co-editors, Professors Yoichi Takakusagi and Tatsuya Kawai. And, I aslso thank to Professors Masayuki Matsuo, Fuminori Hyodo, Neckers Leonard and Murali C. Krishna for fruitful discussion.

    Keywords: Cancer Metabolism, Glycolysis Oxidative, Phosphorylation, small molecules, Imaging technology, 13C-MRI, clinical application

    Received: 12 Feb 2025; Accepted: 21 Feb 2025.

    Copyright: © 2025 OSHIMA, Aisu, Masuo, Takakusagi and Kawai. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Nobu OSHIMA, Department of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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