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Updated: May 8, 2026

Exploring the Pharmacological Action and Molecular Mechanism of Salidroside in Inhibiting MCF-7 Cell Proliferation and Migration
Published on: June 9, 2023
Vitamin D3 and K2-loaded keratin nanoparticles inhibit breast cancer cell growth via MCM-7 downregulation and ROS
Sunny Mukherjee1, Kumari Bhavya2, Siddhartha Dan3
1Department of Biotechnology, Dr. B.R. Ambedkar National Institute of Technology, Jalandhar, Punjab, 144008, India; Department of Biomedical Engineering, Indian Institute of Technology Hyderabad, Kandi, Telangana, 502284, India.
Abstract:
The overexpression of the MCM-7 gene, a key player in the minichromosomal maintenance complex critical for DNA replication initiation, is linked to various aggressive cancers. Despite MCM-7's importance in cancer therapy, its amino acid structure has only recently been elucidated, and no clinical trials with small molecular antagonists have been pursued. The present study highlights the anticancer potential of vitamins D2, D3, and K2-loaded keratin nanoparticles, exploring a novel approach to cancer treatment. We found that NPD3 and NPK2 have more anti-proliferative effects than NPD2 through rigorous in-vitro assays utilizing the MCF-7 human breast cancer cell line, known for MCM-7 overexpression. Mechanistically, NPD3 exerts its anticancer effect by downregulating MCM-7 protein expression, while NPK2 induces intracellular ROS generation. The study involves a nanocarrier system derived from human hair keratin, enhancing the bioavailability and efficacy of these vitamins. These nanocarriers not only improve the anti-proliferative effects of the vitamins but also demonstrated exceptional biocompatibility and controlled drug release in response to pH changes. These findings propose a novel, commercially viable delivery system for water-insoluble vitamins, offering a promising therapeutic avenue against cancers with MCM-7 overexpression.
Insights
Vitamins D2, D3, and K2 loaded into keratin nanoparticles show anticancer effects against MCM-7 overexpressing cancers. NPD3 downregulates MCM-7, while NPK2 generates ROS, offering a novel therapeutic strategy.
Area of Science:
- Biochemistry
- Nanotechnology
- Oncology
Background:
- MCM-7 gene overexpression is linked to aggressive cancers.
- MCM-7 is crucial for DNA replication initiation.
- Novel therapeutic strategies targeting MCM-7 are needed.
Purpose of the Study:
- To investigate the anticancer potential of vitamin D2, D3, and K2 loaded keratin nanoparticles (NPD2, NPD3, NPK2).
- To explore a novel nanocarrier system for water-insoluble vitamins.
- To evaluate the efficacy against MCM-7 overexpressing breast cancer cells.
Main Methods:
- In-vitro assays using MCF-7 human breast cancer cell line.
- Keratin-based nanocarrier system development for vitamin delivery.
- Assessment of anti-proliferative effects, MCM-7 protein expression, and intracellular ROS generation.
Main Results:
- NPD3 and NPK2 demonstrated superior anti-proliferative effects compared to NPD2.
- NPD3 downregulated MCM-7 protein expression.
- NPK2 induced intracellular reactive oxygen species (ROS) generation.
- Keratin nanoparticles enhanced vitamin bioavailability and exhibited pH-responsive controlled release.
Conclusions:
- Vitamin-loaded keratin nanoparticles offer a promising therapeutic approach for MCM-7 overexpressing cancers.
- The developed nanocarrier system is biocompatible and commercially viable.
- This study presents a novel delivery system for water-insoluble vitamins in cancer therapy.
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