| Literature DB >> 26364852 |
Gemma Ferrer-Mayorga1, Silvia Alvarez-Díaz1, Noelia Valle1, Javier De Las Rivas2, Marta Mendes3, Rodrigo Barderas3, Francesc Canals4, Olga Tapia5, J Ignacio Casal3, Miguel Lafarga5, Alberto Muñoz6.
Abstract
Cystatin D is an inhibitor of lysosomal and secreted cysteine proteases. Strikingly, cystatin D has been found to inhibit proliferation, migration, and invasion of colon carcinoma cells indicating tumor suppressor activity that is unrelated to protease inhibition. Here, we demonstrate that a proportion of cystatin D locates within the cell nucleus at specific transcriptionally active chromatin sites. Consistently, transcriptomic analysis show that cystatin D alters gene expression, including that of genes encoding transcription factors such as RUNX1, RUNX2, and MEF2C in HCT116 cells. In concordance with transcriptomic data, quantitative proteomic analysis identified 292 proteins differentially expressed in cystatin D-expressing cells involved in cell adhesion, cytoskeleton, and RNA synthesis and processing. Furthermore, using cytokine arrays we found that cystatin D reduces the secretion of several protumor cytokines such as fibroblast growth factor-4, CX3CL1/fractalkine, neurotrophin 4 oncostatin-M, pulmonary and activation-regulated chemokine/CCL18, and transforming growth factor B3. These results support an unanticipated role of cystatin D in the cell nucleus, controlling the transcription of specific genes involved in crucial cellular functions, which may mediate its protective action in colon cancer.Entities:
Keywords: colon cancer; cysteine protease; cytokine; gene expression; protease inhibitor
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Year: 2015 PMID: 26364852 PMCID: PMC4646312 DOI: 10.1074/jbc.M115.660175
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157