Abstract

BackgroundLactoferrins exhibit antitumoral activities either as a secretory lactoferrin or an intracellular delta-lactoferrin isoform. These activities involve processes such as regulation of the cell cycle and apoptosis. While lactoferrin has been shown to exert its function by activating different transduction pathways, delta-lactoferrin has been proven to act as a transcription factor. Like many tumor suppressors, these two proteins are under-expressed in several types of cancer, particularly in breast cancer.Methodology/Principal FindingsIn order to compare the differential effects of the re-introduction of lactoferrin isoforms in breast cancer cells we chose the cancerous mammary gland MDA-MB-231 cell line as a model. We produced a cell line stably expressing delta-lactoferrin. We also treated these cells with fresh purified human breast lactoferrin. We performed two quantitative proteomic studies in parallel using SILAC coupled to mass spectrometry in order to compare the effects of different doses of the two lactoferrin isoforms. The proteome of untreated, delta-lactoferrin expressing and human lactoferrin treated MDA-MB-231 cells were compared. Overall, around 5300 proteins were identified and quantified using the in-house developed MFPaQ software. Among these, expression was increased by 1.5-fold or more for around 300 proteins in delta-lactoferrin expressing cells and 190 proteins in lactoferrin treated cells. At the same time, about 200 and 40 proteins were found to be downregulated (0-0.7-fold) in response to delta-lactoferrin and lactoferrin, respectively.Conclusions/SignificanceRe-introduction of delta-lactoferrin and lactoferrin expression in MDA-MB-231 mainly leads to modifications of protein profiles involved in processes such as proliferation, apoptosis, oxidative stress, the ubiquitin pathway, translation and mRNA quality control. Moreover, this study identified new target genes of delta-lactoferrin transcriptional activity such as SelH, GTF2F2 and UBE2E1.

Highlights

  • Over the last decade, it has become clear that lactoferrin isoforms have a role as anti-tumoral agents and behave as tumor suppressors

  • We demonstrated that DLf is capable of activating the expression of Skp1 [13], a protein belonging to Skp1-Cul1-Fbox protein (SCF) complex, one of the most well characterized types of ubiquitin ligase (E3), DcpS [47], a pyrophosphatase responsible for mRNA decapping and Bax [42], a pro-apoptotic component

  • Our results showed that re-introduction of Lf or DLf expression in MDA-MB-231 cells mainly leads to modifications of protein profiles involved in processes such as proliferation, apoptosis, oxidative stress, ubiquitin pathway, translation and mRNA quality control

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Summary

Introduction

It has become clear that lactoferrin isoforms have a role as anti-tumoral agents and behave as tumor suppressors. Our results showed that re-introduction of Lf or DLf expression in MDA-MB-231 cells mainly leads to modifications of protein profiles involved in processes such as proliferation, apoptosis, oxidative stress, ubiquitin pathway, translation and mRNA quality control.

Results
Conclusion
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