ReviewCancer pathogenesis and therapy2026
Methionine restriction for cancer therapy: From preclinical studies to clinical trials.
Review in Cancer pathogenesis and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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.
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.
Who cites it
11 citing papers in PubMed.
- Significance of GSH and HRedox report : communications in free radical research · 2026Review
- Immunometabolism and rheumatic disease-advancing targeted therapies.EULAR rheumatology open · 2026Review
- Methionine Regulates Antitumour Function of CD8Immunology · 2026Article
- Boosting CAR T cell efficacy in cancer with metabolic insights from design to diet.Nature reviews. Cancer · 2026Review
- Review
- The Impact of Diet on Long-Term Oncological Outcomes: Investigating Nutritional Mechanisms in Cancer Prevention Management and Prognosis.Nutrients · 2026Review
- Intersection of Precision Nutrition and Bladder Cancer: A Narrative State-of-the-Art Review of Potential Applications and Challenges.Journal of clinical medicine · 2026Review
- The Double-Edged Nature of Methyl Donors in Cancer Development from Prevention to Progression.International journal of molecular sciences · 2025Review
- Methionine regulates antitumor function of CD8bioRxiv : the preprint server for biology · 2025Article
- Synergy of a Low-methionine Diet and Reduced-dose Cisplatinum Eradicates Experimental Lung-cancer Bone Metastases in a Nude-mouse Model.In vivo (Athens, Greece)Article
- The Combination of Methionine Adenosyltransferase 2A (MAT2A) Inhibitor AG-270 and Recombinant Methioninase Is Not Cancer-selective in a Co-culture Model of Colon Cancer Cells and Normal Fibroblasts.Cancer diagnosis & prognosisArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Methionine restriction (MR) has shown significant promise in cancer therapy because it targets the unique methionine dependency of many tumors. However, despite extensive research on MR, a clear synthesis of preclinical findings and their translation into clinical settings is lacking. This review aims to address this gap by consolidating existing evidence, identifying challenges, and highlighting opportunities for advancing MR as a viable cancer treatment strategy. Preclinical studies have revealed that MR effectively hinders cancer cell proliferation, triggers cell cycle arrest, and enhances the effectiveness of standard treatments, including chemotherapy and radiotherapy. Mechanistically, MR disrupts critical cancer pathways by influencing epigenetic regulation, redox balance, and autophagy. Moreover, animal models have demonstrated notable tumor suppression and extended survival, underscoring the therapeutic potential of MR. Early-phase clinical trials are now examining MR in combination with established therapies, reporting positive preliminary results regarding safety and tolerability, and investigating biomarkers for predicting patient responsiveness. These findings suggest the utility of MR as a complementary treatment strategy, particularly for tumors resistant to conventional therapies. The outcomes of this study underscore the importance of further research to refine MR protocols, understand long-term effects, and identify optimal patient groups. Furthermore, combining MR with immunotherapies, targeted treatments, and advanced modalities such as chimeric antigen receptor (CAR)-T cell therapy may offer new therapeutic pathways. Additionally, the development of MR-mimetic drugs and targeted supplements can improve patient compliance and broaden the therapeutic applicability of MR. Large-scale clinical trials are essential to evaluate the efficacy of MR across diverse cancer types, focusing on sustainability and safety over extended periods. If successful, MR can transform cancer therapy by exploiting metabolic vulnerabilities in cancer cells, providing a novel and less toxic treatment option for challenging malignancies.
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Registered trials
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.