Abstract

Nanomaterials with unique characteristics exhibit favorable therapeutic and diagnostic properties, implying their enormous potential as biomedical candidates. C60 has been used in gene- and drug-delivery, as imaging agents, and as photosensitizers in cancer therapy. In this study, the influences of a cationic functionalized fullerene on cellular behavior of human colorectal cancer cell line (HT-29) were investigated. Results indicated that HT-29 treated with the studied compound showed a lower sensitivity but a significant impairment in migration and invasion by interfering with the activities of matrix metalloproteinases (MMP-2 and 9). The presence of fullerene also altered the capacity of adhesion-related proteins to perform their activity, thereby inducing dramatically adverse effects on the cell physiological functions such as cell adhesion. Thus, our study suggests that this compound is a new potential anti-metastatic effector and a therapeutic component for malignant colorectal cancer.

Highlights

  • Current status of anticancer chemotherapy of solid malignant tumors indicates the necessity for agents active against tumor metastases

  • The present study examined the hypothesis that derivative C60+ participates in colorectal cancer cell invasion

  • C60+ caused a statistically significant reduction of cell viability, as determined by the MTT test only at the highest dose tested, being the other dosages only marginally capable to influence HT-29 cell growth during the experiment. This result is consistent with unpublished data showing different degrees of cytotoxicity of this fullerene derivative in vitro on a number of tumor cell lines: MCF7 cells were sensitive to the cytotoxic effects [9], whereas other cell lines, e.g. MDA-MB231, were much less sensitive, as reported here for HT-29 cells

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Summary

Introduction

Current status of anticancer chemotherapy of solid malignant tumors indicates the necessity for agents active against tumor metastases. [60] Fullerene Derivative Reduces Invasion and Migration of HT-29 CRC Cells in Vitro at Dose Free of Significant Effects on Cell Survival”, Nano-Micro Lett.

Results
Conclusion

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