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Simple Summary: Surgical metastasectomy has been the primary choice for local therapy in patients with lung metastasis secondary to sarcoma. Over recent decades, however, stereotactic body radiation therapy (SBRT) has been employed more extensively in the treatment of lung metastasis. SBRT is associated with less toxicity and similar outcomes compared with surgical metastasectomy. When used with chemotherapy and surgery in a multimodal treatment plan, SBRT can improve the cure rate and prolong survival. Background: Stereotactic body radiotherapy (SBRT) is increasingly used to treat lung metastasis (LM) in patients with soft tissue sarcoma (STS) and bone sarcoma (BS). Methods: This retrospective study evaluated the outcomes of patients with BS and STS treated with SBRT for LM between 2010 and 2023. Results: We enrolled 102 patients (51 each with STS and BS), of whom 71 were males and 31 were females (median age, 40 years; range, 11–81 years). At diagnosis, 76 and 26 patients had localized and metastatic disease, respectively, with a median of 4 recurrences (range, 1–12). Before SBRT, 75 patients received chemotherapy and 52 underwent surgery for LM, with 276 nodules treated with SBRT (median dose, 48 Gy; range, 40–52). Local control of irradiated LM was 86% at 1 year and 78% at 2 years. By 31 December 2023 (median follow-up, 4.8 years), 60 patients had died and 42 survived (20 without ongoing disease). From the first LM relapse, the median overall survival (OS) was 4.8 years and the 5-year OS was 49% (95% confidence interval, 39–60%), with no difference between STS and BS; the median OS was 2.9 years and the 5-year OS was 36% after SBRT. Chemotherapy before SBRT was a negative prognostic factor by multivariate analysis. Conclusions: Long-term follow-up shows that SBRT as part of a multimodal treatment approach has reasonable survival rates in patients with LM due to sarcoma. Compared with historical results using only surgery and chemotherapy, SBRT has improved the 5-year OS. [ABSTRACT FROM AUTHOR]

Sulforaphane is considered the bioactive metabolite of glucoraphanin after dietary consumption of broccoli sprouts. Although both molecules pass through the gut lumen to the large intestine in stable form, their biological impact on the first intestinal tract is poorly described. In celiac patients, the function of the small intestine is affected by celiac disease (CD), whose severe outcomes are controlled by gluten-free dietary protocols. Nevertheless, pathological signs of inflammation and oxidative stress may persist. The aim of this study was to compare the biological activity of sulforaphane with its precursor glucoraphanin in a cellular model of gliadin-induced inflammation. Human intestinal epithelial cells (CaCo-2) were stimulated with a pro-inflammatory combination of cytokines (IFN-γ, IL-1β) and in-vitro-digested gliadin, while oxidative stress was induced by H2O2. LC-MS/MS analysis confirmed that sulforaphane from broccoli sprouts was stable after simulated gastrointestinal digestion. It inhibited the release of all chemokines selected as inflammatory read-outs, with a more potent effect against MCP-1 (IC50 = 7.81 µM). On the contrary, glucoraphanin (50 µM) was inactive. The molecules were unable to counteract the oxidative damage to DNA (γ-H2AX) and catalase levels; however, the activity of NF-κB and Nrf-2 was modulated by both molecules. The impact on epithelial permeability (TEER) was also evaluated in a Transwell® model. In the context of a pro-inflammatory combination including gliadin, TEER values were recovered by neither sulforaphane nor glucoraphanin. Conversely, in the context of co-culture with activated macrophages (THP-1), sulforaphane inhibited the release of MCP-1 (IC50 = 20.60 µM) and IL-1β (IC50 = 1.50 µM) only, but both molecules restored epithelial integrity at 50 µM. Our work suggests that glucoraphanin should not merely be considered as just an inert precursor at the small intestine level, thus suggesting a potential interest in the framework of CD. Its biological activity might imply, at least in part, molecular mechanisms different from sulforaphane. [ABSTRACT FROM AUTHOR]

ABSTRACT Shifts in species distribution have far‐reaching implications across ecological, economic, and social dimensions. Pelagic fish, integral to global fisheries, have displayed notable euryhaline and eurythermal characteristics. However, a poleward range expansion trend has emerged in the northern hemisphere for certain Scomber species since the 2010s, attributed to sea surface temperature and food resource dynamics. Scomber colias, a principal pelagic fishery resource in Argentina, stands as an underexploited species with recent landings totaling approximately 14,800 tons. In the North Patagonian shelf waters, where S. colias resides at its southern distribution, there has been documented ocean warming. In this context, this study evaluates potential changes in the distribution and abundance of S. colias from 1991 to 2022 in the Southwestern Atlantic Ocean (SAO). Drawing on two distinct data sources, the analysis reveals a poleward range expansion, extending to 48°5′S, exceeding historical limits by 278 km. This expansion is positively correlated with rising sea surface temperatures, with the most significant displacement observed during summer, when this species has a high feeding activity in the study area. The investigation further explores the relationship between S. colias presence and the abundance of its primary prey species between 2011 and 2022. This is highly possible, yet no significant results were uncovered. This study marks the first documented southward range expansion of S. colias in the SAO, providing essential quantitative insights for biological studies, fisheries management, and the canning manufacturing industry. The latter could benefit from year‐round access to fish, potentially generating employment opportunities and fostering economic growth within the local community. [ABSTRACT FROM AUTHOR]