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Biology subjects

Coelho, A. R.

Publications and source records attributed to Coelho, A. R..

2 recordsLinked to original sources

Bifunctional Phagocytic Synapse Enhancers for Cancer Immunotherapy

Immunotherapy profoundly impacted cancer treatments by harnessing the patients immune system. Phagocytosis, the process whereby immune cells engulf and destroy foreign particles or cells, plays a critical role in tumour cell clearance. Herein, we introduce a novel concept termed "ENPHASYS" - Enhancement of Phagocytic Synapses - designed to direct and amplify phagocytosis of cancer cells using heterobifunctional molecules named phagocytic synapse enhancers (PSEs). By engineering a de novo PD-L1 binder linked to a natural phagocytosis promoting peptide, tuftsin, the resulting PSE combines PD-L1 blockade with enhanced tumour cell phagocytosis; in addition, the PSEs induce macrophages to internalize a membrane or extracellular target. Intratumoural treatment of colorectal carcinoma- or glioblastoma-burdened immunocompetent animals resulted in beneficial overall survival, delayed tumour growth and a potent antitumor response driven by T-cell activation and TAM reprogramming, underpinning the translational relevance of ENPHASYS. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=118 SRC="FIGDIR/small/642658v1_ufig1.gif" ALT="Figure 1"> View larger version (19K): org.highwire.dtl.DTLVardef@1673fd4org.highwire.dtl.DTLVardef@18fa319org.highwire.dtl.DTLVardef@11cf680org.highwire.dtl.DTLVardef@7b8784_HPS_FORMAT_FIGEXP M_FIG C_FIG

cancer biology↗

Peroxidasin expression is increased in intratumoural capillaries and in proximal tubular cells adjacent to clear cell renal cell carcinoma.

Peroxidasin (PXDN), is a heme peroxidase with a critical role in the crosslinking of type IV collagen, being essential for basement membrane integrity. In many cancers, PXDN overexpression has been linked with processes associated with poor disease outcomes, namely the impairment of endothelial functions, pathogenesis of vascular diseases, vascular remodelling, apoptosis, and tissue fibrosis. In RCC, almost nothing is so far known. In this work we characterized the expression of PXDN in tumour and non-neoplastic adjacent tissue from clear cell renal cell carcinoma (ccRCC) and renal oncocytoma by immunohistochemistry. Results showed a significant increase of PXDN expression in intratumoural capillaries of ccRCC in comparison with oncocytoma, and an increase in the proximal tubular epithelial cells of non-neoplastic adjacent parenchyma from ccRCC cases, in comparison with the same area from oncocytomas. Overall, our results suggest, for the first time, that PXDN may have a role in tumour angiogenesis that may favour metastases and tumour malignity, being also enrolled in the crosstalk between the tumour and adjacent tissue, that deserves further investigation. HighlightsO_LIPeroxidasin is increased in ccRCC microvasculature comparing to oncocytoma. C_LIO_LIPeroxidasin is increased in proximal tubules of ccRCC kidney adjacent parenchyma. C_LIO_LIIs Peroxidasin a modulator of tumour microenvironment promoting angiogenesis? C_LI

pathology↗