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PLoS One. 2018 Apr 12;13(4):e0195542. doi: 10.1371/journal.pone.0195542. eCollection 2018.

Inducing cell death in vitro in cancer cells by targeted delivery of cytochrome c via a transferrin conjugate.

Author information

1
Department of Environmental Sciences, University of Puerto Rico, Rio Piedras Campus, San Juan, Puerto Rico, United States of America.
2
Department of Chemistry, University of Puerto Rico, Rio Piedras Campus, San Juan, Puerto Rico, United States of America.

Abstract

One of the major drawbacks of many of the currently used cancer drugs are off-target effects. Targeted delivery is one method to minimize such unwanted and detrimental events. To actively target lung cancer cells, we have developed a conjugate of the apoptosis inducing protein cytochrome c with transferrin because the transferrin receptor is overexpressed by many rapidly dividing cancer cells. Cytochrome c and transferrin were cross-linked with a redox sensitive disulfide bond for the intra-cellular release of the protein upon endocytosis by the transferrin receptor. Confocal results demonstrated the cellular uptake of the cytochrome c-transferrin conjugate by transferrin receptor overexpressing A549 lung cancer cells. Localization studies further validated that this conjugate escaped the endosome. Additionally, an in vitro assay showed that the conjugate could induce apoptosis by activating caspase-3. The neo-conjugate not only maintained an IC50 value similar to the well known drug cisplatin (50 μM) in A549 cancer cells but also was nontoxic to the normal lung (MRC5) cells. Our neo-conjugate holds promise for future development to target cancers with enhanced transferrin receptor expression.

PMID:
29649293
PMCID:
PMC5896948
DOI:
10.1371/journal.pone.0195542
[Indexed for MEDLINE]
Free PMC Article

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