Exosomes are extracellular vesicles found in saliva and other body fluids. These vesicles range in size from 30 to 150 nm and play a crucial role in intercellular communication, transporting different biomolecules, actively targeting cells. These vesicles regulate both physiological and pathological processes within recipient cells. MicroRNAs (miRs) are transported within exosomes and are delivered to target cells where they influence signaling pathways, taking on a crucial regulatory role in oncogenesis; for example, they are implicated in progression and infiltration of various cancers, such as head and neck squamous cell carcinoma (HNSCC). A systematic literature search based on specific keywords, according to the PRISMA guidelines, was carried out on PubMed, Web of Science, Scopus, and Google Scholar. Only original articles were selected during this review. The risk of bias was assessed by QUADAS-2. At the end of the selection process 9 articles were included. In these studies, 41 miRs showed differential expression between healthy subjects and patient with HNSCC. The techniques varied among studies for the extraction and analysis of exosomal miRs. We presented also salivary exosomal miRs pathways, to give insights about pathogenetic mechanisms. Exosomal microRNA are promising biomarkers for HNSCC detection. MiR-10b-5p, miR-486-5p, miR-24-3p, miR-412-3p, and miR-512-3p are the most promising markers applicable to diagnostics, while miR-1307-5p and miR-519c-3p resulted overexpressed and correlated to worse survival outcomes.

Solenopsis invicta, a South American ant species from the Formicidae family (subfamily Myrmicinae), has recently established a stable settlement in Europe, raising public health concerns due to its venomous stings. The venom of S. invicta is rich in bioactive molecules, particularly piperidine alkaloids such as solenopsin A and peptides (Sol 1–4). These compounds have been implicated in various health applications, including antimicrobial, anti-inflammatory, and antitumour activities. While previous reviews have focused on the ecological and allergenic risks posed by S. invicta, this scoping review aims to evaluate the potential therapeutic uses of S. invicta venom by summarizing existing scientific evidence and providing a novel synthesis of recent research on its bioactive components. Furthermore, this study, by describing the unique biological aspects of S. invicta, provides an overview of its direct impact on public health, highlighting new findings on the venom’s role in inhibiting bacterial biofilm formation and modulating cancer growth pathways through gene regulation. A search of databases (PubMed, Scopus, Science Direct, and Cochrane Library) identified 12,340 articles, from which 11 studies met the eligibility criteria. These studies included seven microbiological investigations and four studies on tumour cell lines and animal models. The findings suggest that S. invicta venom could inhibit biofilm formation, combat fungal infections, and suppress tumour growth. However, further research, including clinical trials, is required to fully elucidate the safety and efficacy of these bioactive molecules in human medicine, for their potential use in drug discovery to counteract several diseases, including cancer.

Microgravity exposure affects both tissues and cells, and, in this regard, one of the most affected targets is the skeletal muscle system due to the significant loss of bone and muscle mass leading to osteoporosis and sarcopenia, respectively. Several efforts are underway to counteract the effects of microgravity, and recent studies on irisin, a myokine with anabolic effects on the musculoskeletal system, have shown promising results. Due to the practical challenges of conducting experiments in actual microgravity, different devices generating a simulated microgravity condition on Earth have been developed. Here, we exposed myoblasts, osteoblasts, osteocytes to a random position machine (RPM) for five days to assess microgravity effect on the expression of key differentiation factors in cells untreated or treated with irisin. In myoblasts (C2C12), exposure to RPM led to increased expression of early myogenesis maker genes Pax7 ( p = 0.0016), Myf5 ( p = 0.0005) and MyoD ( p = 0.0009). Irisin treatment in the last 8 h of RPM cultures prevented these increases by returning Pax7 ( p = 0.0008) and MyoD ( p = 0.01) to control values, and only partially Myf5 . In bone cells, exposure to RPM for 5 days showed no effect in osteoblasts (MC3T3) but decreased the expression of Pdpn ( p = 0.0285) and Dmp‐1 ( p = 0.0423) genes in osteocytes (MLO‐Y4). Irisin treatment completely prevented the decline in Pdpn ( p = 0.293) and Dmp‐1 ( p = 0.0339) levels. Overall, our data showed that the impact of RPM exposure keeps myoblasts and osteocytes in a proliferative state, and irisin treatment restores them to their baseline biological condition, suggesting that irisin can counteract the changes induced by simulated microgravity.

Objectives: The radiographic diagnosis of dental caries is often complicated by the presence of radiographic optical effects, such as the Mach band effect and triangular-shaped radiolucencies (TSR). These phenomena can give rise to false-positive diagnoses, especially in bite-wing radiographs, thus influencing clinical decision-making and possibly leading to overdiagnosis and overtreatment. The aim of this systematic review and meta-analysis was to clarify the real prevalence of these radiographic optical effects in dental radiographs and to quantify their influence on diagnostic errors in caries detection. Methods: This systematic literature review follow the PRISMA guidelines and registered in PROSPERO (CRD420251083823), prior to its execution. Electronic searches were conducted on PubMed, Scopus and the Cochrane Library, with the addition of Grey literature and references of the main reviews on the topic. Inclusion criteria included clinical, in vitro and ex vivo studies evaluating the impact of TSR and Mach band effects on intraoral radiographs (bitewing or periapical), reporting diagnostic performance, prevalence or misinterpretation rates. Data extraction and risk of bias assessment (AXIS, QUADAS-2) were performed independently by two reviewers. Meta-analyses were performed using random effects models. Results: Of 640 identified reports, only five studies were included. The overall prevalence of non-carious TSR on maxillary molars was 26.44%, 270/1021. The meta-analysis showed that effects (TSR or Mach band) led to false positive diagnoses of caries or fractures, in approximately 13% of observations (60/464). Heterogeneity was high (I² > 90%) and the certainty of the evidence was classified as low to very low due to the type of studies included and the consistency indices. Conclusions: Radiographic optical effects, especially TSR and Mach band effect, are highly prevalent in bitewing images and significantly increase the risk of false positive caries diagnoses, especially in children. Given the low certainty of the available evidence, clinicians should interpret radiographic findings with caution and always correlate them with a thorough clinical examination. Further high-quality research is needed to develop standardized diagnostic criteria and strategies to mitigate radiographic optical effects in dental practice.

Head and neck squamous cell carcinoma (HNSCC) is the most common and aggressive histologic subtype of head and neck cancer (HNC), difficult to treat effectively. Here, we discuss several studies on human and mouse HNSCC cell lines arising from the mucosal epithelium of various anatomical sites, as well as recent studies using murine models, focused on targeting key checkpoints in the glutamine (Gln) metabolism pathway, either alone or in synergy with other signaling pathways, as a potential therapeutic strategy for HNSCC. Emerging evidence demonstrates a complex interplay between Gln metabolism and pathways mediating altered cellular mechanisms, including ferroptosis, immune system evasion, mitochondrial energy production, and oncogenic transcriptional control. This review examines currently available gene expression databases and protein expression analyses of Gln metabolism-related components in tissue samples from HNSCC patients. From a translational perspective, the co-administration of pharmaceutical agents and biologic products targeting distinct molecular pathways, integrated with radiotherapy (RT) or chemotherapy (CT), may produce superior anti-HNSCC efficacy, thereby improving clinical outcomes and extending patient survival. Multimodal strategies represent a key direction in precision oncology, enabling personalized therapeutic interventions to suppress metastatic dissemination and disease progression more effectively. Therefore, an integrated therapeutic approach represents a promising path to defeat HNSCC.