Formononetin-derived quantum dots suppress colon cancer growth by triggering mitochondrial apoptosis.
Formononetin (FMN) is an extracted component of traditional Chinese medicine with anticancer effects, but its poor water solubility and low bioavailability have limited further research and applicatio
APA
Zhang J, Cui Y, et al. (2026). Formononetin-derived quantum dots suppress colon cancer growth by triggering mitochondrial apoptosis.. Nanomedicine (London, England), 21(4), 485-497. https://doi.org/10.1080/17435889.2026.2615097
MLA
Zhang J, et al.. "Formononetin-derived quantum dots suppress colon cancer growth by triggering mitochondrial apoptosis.." Nanomedicine (London, England), vol. 21, no. 4, 2026, pp. 485-497.
PMID
41527441
Abstract
Formononetin (FMN) is an extracted component of traditional Chinese medicine with anticancer effects, but its poor water solubility and low bioavailability have limited further research and application. Therefore, based on FMN that is the natural antitumor agent, we synthesized a formononetin quantum dots (FMNQDs) for colon cancer therapy, which has the advantages of outstanding water solubility, homogeneous particle size (2.03 ± 1.0 nm), exceptional stability and good intracellular fluorescence imaging effect. The results show that FMNQD exhibits good antitumor activity by inducing mitochondrial-mediated apoptosis, characterized by elevated intracellular reactive oxygen species (ROS) levels, decreased mitochondrial membrane potential (MMP), and modulated expression of Bax and Bcl-2. In validation confirmed FMNQD's significant tumor growth inhibition. The tumor inhibition rate in the 8 mg/kg dose group was as high as 60.06 ± 6.22%. Moreover, blood biochemical analysis suggested a favorable safety profile. This study establishes FMNQDs as a potential therapeutic agent for colon cancer, providing preclinical evidence to support further development of formononetin-based nanomedicines.
MeSH Terms
Isoflavones; Quantum Dots; Apoptosis; Colonic Neoplasms; Animals; Humans; Mitochondria; Mice; Reactive Oxygen Species; Membrane Potential, Mitochondrial; Cell Line, Tumor; Antineoplastic Agents; Mice, Inbred BALB C; Xenograft Model Antitumor Assays
같은 제1저자의 인용 많은 논문 (5)
- Mitochondria in situ releasing corosolic acid enhanced antitumor effects via activating mitophagy in castration-resistant prostate cancer.
- [Exploring the intervention mechanism of modified Danggui buxue decoction on neuroinflammation in CIPN model mice based on transcriptomics and network pharmacology].
- Injectable HMME-Loading Emulsion Hydrogel for Ultrasound-Triggered Release and Enhanced Sonodynamic Immunotherapy.
- Bilaterality in papillary thyroid carcinoma: long-term outcomes and predictive factors.
- Identification of a 9-gene autophagy-related signature for predicting prognosis and immune exhaustion features in breast cancer.