1. Academic Validation
  2. A nano-platform combats the "attack" and "defense" of cytoskeleton to block cascading tumor metastasis

A nano-platform combats the "attack" and "defense" of cytoskeleton to block cascading tumor metastasis

  • J Control Release. 2024 Feb 5:367:572-586. doi: 10.1016/j.jconrel.2024.01.069.
Jing Tao 1 Yuan Yao 1 Minyi Huang 1 Jiahui Wu 1 Jiayan Lyu 1 Qiuyi Li 1 Lian Li 1 Yuan Huang 1 Zhou Zhou 2
Affiliations

Affiliations

  • 1 Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, PR China.
  • 2 Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, PR China. Electronic address: zhou_zhou610@163.com.
Abstract

The Cytoskeleton facilitates tumor cells invasion into the bloodstream via vasculogenic mimicry (VM) for "attack", and protects cells against external threats through cytoskeletal remodeling and tunneling nanotubes (TNTs) for "defense". However, the existing strategies involving Cytoskeleton are not sufficient to eliminate tumor metastasis due to mitochondrial energy supply, both within tumor cells and from outside microenvironment. Here, considering the close relationship between Cytoskeleton and mitochondria both in location and function, we construct a nano-platform that combats the "attack" and "defense" of Cytoskeleton in the cascading metastasis. The nano-platform is composed of KFCsk@LIP and KTMito@LIP for the cytoskeletal collapse and mitochondrial dysfunction. KFCsk@LIP prevents the initiation and circulation of cascading tumor metastasis, but arouses limited suppression in tumor cell proliferation. KTMito@LIP impairs mitochondria to trigger Apoptosis and impede energy supply both from inside and outside, leading to an amplified effect for metastasis suppression. Further mechanisms studies reveal that the formation of VM and TNTs are seriously obstructed. Both in situ and circulating tumor cells are disabled. Subsequently, the broken metastasis cascade results in a remarkable anti-metastasis effect. Collectively, based on the nano-platform, the cytoskeletal collapse with synchronous mitochondrial dysfunction provides a potential therapeutic strategy for cascading tumor metastasis suppression.

Keywords

Cascading tumor metastasis; Cytoskeletal collapse; Mitochondrial dysfunction; Tunnel nanotubes; Vasculogenic mimicry.

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