Artificial light at night alters the locomotor behavior of the Mediterranean sea urchin Paracentrotus lividus.

Artificial light at night (ALAN) is a recognized source of anthropogenic disturbance, although its effects on biological systems have not been fully explored. Within marine ecosystems, coastal areas are the most impacted by ALAN. Here, we focused on the Mediterranean sea urchin Paracentrotus lividus, which has a crucial role in shaping benthic ecosystems. Our objective was to investigate if ALAN affects the nocturnal locomotor behavior of P. lividus. A semi-controlled field study was conducted along a rocky shore near a promenade lit at night. Results suggested a potential impact of ALAN on the locomotor behavior of sea urchins. Individuals of P. lividus tended to move away from the light sources while its directions in dark conditions were uniform. Their locomotor performance, in presence of ALAN, was characterized by shorter latency time, lower sinuosity and higher mean speed at increasing light intensity, with potential cascading effect at the ecosystem level.

CD44: A New Prognostic Marker in Colorectal Cancer?

Cluster of differentiation 44 (CD44) is a non-kinase cell surface glycoprotein. It is overexpressed in several cell types, including cancer stem cells (CSCs). Cells overexpressing CD44 exhibit several CSC traits, such as self-renewal, epithelial-mesenchymal transition (EMT) capability, and resistance to chemo- and radiotherapy. The role of CD44 in maintaining stemness and the CSC function in tumor progression is accomplished by binding to its main ligand, hyaluronan (HA). The HA-CD44 complex activates several signaling pathways that lead to cell proliferation, adhesion, migration, and invasion. The CD44 gene regularly undergoes alternative splicing, resulting in the standard (CD44s) and variant (CD44v) isoforms. The different functional roles of CD44s and specific CD44v isoforms still need to be fully understood. The clinicopathological impact of CD44 and its isoforms in promoting tumorigenesis suggests that CD44 could be a molecular target for cancer therapy. Furthermore, the recent association observed between CD44 and KRAS-dependent carcinomas and the potential correlations between CD44 and tumor mutational burden (TMB) and microsatellite instability (MSI) open new research scenarios for developing new strategies in cancer treatment. This review summarises current research regarding the different CD44 isoform structures, their roles, and functions in supporting tumorigenesis and discusses its therapeutic implications.