Irinotecan/scFv co-loaded liposomes coaction on tumor cells and CAFs for enhanced colorectal cancer therapy

J Nanobiotechnology. 2021 Dec 14;19(1):421. doi: 10.1186/s12951-021-01172-0.

Abstract

Background: Cancer-associated fibroblasts (CAFs), as an important component of stroma, not only supply the "soils" to promote tumor invasion and metastasis, but also form a physical barrier to hinder the penetration of therapeutic agents. Based on this, the combinational strategy that action on both tumor cells and CAFs simultaneously would be a promising approach for improving the antitumor effect.

Results: In this study, the novel multifunctional liposomes (IRI-RGD/R9-sLip) were designed, which integrated the advantages including IRI and scFv co-loading, different targets, RGD mediated active targeting, R9 promoting cell efficient permeation and lysosomal escape. As expected, IRI-RGD/R9-sLip showed enhanced cytotoxicity in different cell models, effectively increased the accumulation in tumor sites, as well as exhibited deep permeation ability both in vitro and in vivo. Notably, IRI-RGD/R9-sLip not only exhibited superior in vivo anti-tumor effect in both CAFs-free and CAFs-abundant bearing mice models, but also presented excellent anti-metastasis efficiency in lung metastasis model.

Conclusion: In a word, the novel combinational strategy by coaction on both "seeds" and "soils" of the tumor provides a new approach for cancer therapy, and the prepared liposomes could efficiently improve the antitumor effect with promising clinical application prospects.

Keywords: Cancer-associated fibroblasts; Co-cultured cells; Colorectal cancer; Liposomes; Single chain fragment variable.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / pharmacology
  • Apoptosis / drug effects
  • Cancer-Associated Fibroblasts / drug effects*
  • Cell Line, Tumor
  • Coculture Techniques
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / pathology
  • Drug Delivery Systems / methods*
  • Female
  • Irinotecan* / chemistry
  • Irinotecan* / pharmacokinetics
  • Irinotecan* / pharmacology
  • Liposomes* / chemistry
  • Liposomes* / pharmacokinetics
  • Liposomes* / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • NIH 3T3 Cells
  • Single-Chain Antibodies / chemistry
  • Single-Chain Antibodies / pharmacokinetics

Substances

  • Antineoplastic Agents
  • Liposomes
  • Single-Chain Antibodies
  • Irinotecan