ReviewNaunyn-Schmiedeberg's archives of pharmacology2026
Emerging role of plant-based compounds as ferroptosis modulators in breast cancer.
Review in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Computer-aided design, molecular dynamics simulations and in-vitro inhibitory potential of piperazine bridged bis-thiadiazole benzothioate derivatives against platelet-derived endothelial cell growth factor.Journal of computer-aided molecular design · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Ferroptosis is a specialized form of regulated cell death that is dependent on intracellular iron and is characterized by excessive lipid peroxidation, accumulation of lipid peroxides, and increased intracellular iron levels. This process is regulated through complex and tightly coordinated molecular mechanisms involving multiple signaling pathways and regulatory proteins, including key antioxidant defense components such as glutathione peroxide 4 (GPX4) and ferroptosis suppressor protein-1 (FSP-1). Increasing experimental evidences suggested that modulation of ferroptosis pathway might offer a potent target for breast cancer management, as ferroptosis dysregulation has been strongly associated with tumor invasion, progression, and drug resistance. Current cancer treatment strategies including surgery, chemotherapy, radiation therapy have detrimental effects on cancer patients. Therefore, it is highly needed to focus on safe and effective therapeutics like natural compounds for cancer therapy. These compounds have shown the significance of ferroptosis-mediated cell death, thereby providing drug candidate for developing ferroptosis-inducing agents. Current research studies suggested that numerous plant-based compounds have strong anticancer potential via ferroptosis induction in breast carcinoma. However, these results are dependent upon preclinical experimentation and lacking validation of long-term clinical research. Thus, this review is designed to provide a mechanistic overview of plant-derived natural compounds by targeting ferroptosis pathway specifically in breast cancer. This could help the researchers working in medicinal chemistry field and pharmacology to better understand the mechanism of action of these compounds against breast carcinoma and provide an alternative approach to treat breast cancer.
Indexed as
Identifiers
42322357What Socratic holds
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 Socratic graph.