Organotin(IV)-loaded mesoporous silica as a biocompatible strategy in cancer treatment

Angew Chem Int Ed Engl. 2014 Jun 2;53(23):5982-7. doi: 10.1002/anie.201400763. Epub 2014 May 14.

Abstract

The strong therapeutic potential of an organotin(IV) compound loaded in nanostructured silica (SBA-15pSn) is demonstrated: B16 melanoma tumor growth in syngeneic C57BL/6 mice is almost completely abolished. In contrast to apoptosis as the basic mechanism of the anticancer action of numerous chemotherapeutics, the important advantage of this SBA-15pSn mesoporous material is the induction of cell differentiation, an effect unknown for metal-based drugs and nanomaterials alone. This non-aggressive mode of drug action is highly efficient against cancer cells but is in the concentration range used nontoxic for normal tissue. JNK (Jun-amino-terminal kinase)-independent apoptosis accompanied by the development of the melanocyte-like nonproliferative phenotype of survived cells indicates the extraordinary potential of SBA-15pSn to suppress tumor growth without undesirable compensatory proliferation of malignant cells in response to neighboring cell death.

Keywords: cell differentiation; cisplatin; drug delivery; melanoma; nanostructures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cell Proliferation
  • Melanoma, Experimental / drug therapy*
  • Mice
  • Mice, Inbred C57BL
  • Nanostructures
  • Neoplasms / therapy*
  • Organotin Compounds / chemistry*
  • Silicon Dioxide / pharmacology*

Substances

  • Organotin Compounds
  • Silicon Dioxide