Bacteria-Assisted Celastrol Liposomes for Effective Chemotherapy Against Lung Cancer in Mice Model.

INTRODUCTION

Lung cancer has a high resistance rate to current chemotherapies. Therefore, there is an urgent need to develop new anticancer drugs. Celastrol is a promising anticancer bioactive compound for various types of cancers. However, its poor solubility and severe liver damage have limited its clinical application.

METHODS

BIF@CEL/LF/CMCS-Lipo (Bif@CLC-LP), a self-driving biomotor that targets tumor tissues, was used to deliver celastrol, which was encapsulated in surface-modified lactoferrin liposomes, which were then coated with carboxymethyl chitosan and loaded onto the surface of (Bif). Extensive in vitro and in vivo experiments were performed to assess its physicochemical and antitumor properties and safety in treating lung cancer.

RESULTS

Bif@CLC-LP responds to pH and is bioselective, precisely targeting hypoxic regions of tumors. In the acidic tumor environment, the carboxymethyl chitosan coating breaks down, releasing liposomes that can specifically target the cancer surface receptor for endocytosis. This process increases the production of reactive oxygen species (ROS) and decreases the mitochondrial membrane potential in lung cancer cells, leading to apoptosis.

CONCLUSION

In our work, Bif@CLC-LP significantly inhibited tumor growth while minimizing celastrol-induced liver damage in a mouse lung cancer model. This bacteria-mediated liposome delivery system is a promising new nanoplatform for treating different types of solid cancer.