The radon concentration activity in buildings is influenced by various factors, including meteorological elements like temperature, pressure, and precipitation, which are recognized as significant influencers. The fluctuations of indoor radon in premises are related to seasonal change. This study aimed to understand better the effects of environmental parameters on indoor radon concentration levels in the Aksu school. Indoor and outdoor temperature differentials heavily influence diurnal indoor radon patterns. The analysis indicates that the correlation between indoor radon and outdoor temperature, dew point, and air humidity is weak and negligible for atmospheric pressure, wind speed, and precipitation, as determined by the obtained values of R² and the Chaddock scale. The multiple regression model is characterized by the correlation coefficient r_xy = 0.605, which corresponds to a close relationship on the Chaddock scale.

Radon is an inert gas produced by the radioactive decay of uranium-238, commonly found in the environment. Radon and its decay products are the main sources of human exposure to radiation from natural sources. When inhaled, radon’s alpha particles impact lung tissue, potentially causing lung cancer by damaging DNA and altering oxidative processes. This review article addresses the need for a deeper understanding of the genetic and molecular changes associated with radon-induced lung cancer, aiming to clarify key genetic mutations and protein markers linked to carcinogenesis. Particular attention in recent studies has been given to mutations in tumor suppressor genes (RASSF1, TP53), oncogenes (KRAS, EGFR), and changes in the expression levels of protein biomarkers associated with inflammation, stress, and apoptosis. Identifying these markers is critical for developing effective screening methods for radon-induced lung cancer, enabling timely identification of high-risk patients and supporting effective preventive strategies. Summarizing current genetic and protein biomarkers, this review highlights the importance of a comprehensive approach to studying radon-induced carcinogenesis. Understanding these molecular mechanisms could ultimately improve early diagnostic methods and enhance therapy for cancers associated with radon exposure.

Among the Central Asian countries, Kazakhstan is experiencing significant growth in uranium production and plays a key role in the mining industry. The aim of this study was to assess environmental gamma radiation levels and indoor radon concentrations in the settlements of Aqsu, Saumalkol, and Arykbalyk—situated in regions with a history of uranium mining activities—to evaluate potential radiation exposure risks to the local population. Measurements of ambient gamma radiation dose rates indicated that Saumalkol exhibited the highest variability, with recorded values reaching up to 0.56 ± 0.19 µSv/h, suggesting potential influence from abandoned mining areas. The equivalent equilibrium volume activity of radon revealed severe contamination in Aqsu (mean: 303 ± 57 Bq/m³, max: 4974 Bq/m³) and Saumalkol (mean: 658 ± 114 Bq/m³, max: 2470 Bq/m³). These findings underscore the need for immediate intervention measures such as improved ventilation and radon mitigation strategies to reduce exposure risks and protect residents from radiation-induced health hazards. This study presents a screening method to identify areas with potential radon risks. However, radon dose assessment requires long-term measurements for accurate evaluation of exposure levels and health risks, with extended monitoring needed for comprehensive assessment.

Residential exposure to radon and environmental gamma radiation poses a significant public health concern in uranium-rich regions. The Akmola Region of Kazakhstan, home to one of the world’s largest uranium tailings sites, lacks localized data on seasonal exposure variations and associated health risks. This study assessed indoor radon progeny concentrations and gamma dose rates in 62 dwellings across two settlements—Aqsu and Zavodskoy—in the Akmola Region during autumn 2023 through summer 2024. Using RAMON-02 and Alpharad Plus detectors, seasonal equivalent equilibrium volumetric activity (EEVA) of radon progeny and effective doses were calculated, stratified by presence of a cellar. In Aqsu, ambient dose equivalent rates reached up to 0.55 µSv/h, and winter median EEVA levels exceeded 130 Bq/m³ in some non-cellar homes. Seasonal effective doses peaked in spring (up to 8.82 mSv) in cellar dwellings, with annual doses reaching 23.5 mSv—substantially higher than in Zavodskoy. Although mitigation efforts have reduced exposure in some homes, several cellar dwellings in Aqsu exhibited persistently elevated EEVA, suggesting potential structural vulnerabilities or residual contamination. These findings underscore significant seasonal and structural disparities in radiation exposure and highlight the need for targeted, site-specific interventions to reduce long-term health risks in affected communities.

Mesenchymal stromal cells (MSCs) are multipotent cells characterized by their regenerative capacity and strong immunomodulatory properties. In recent years, MSC-based therapy has attracted significant attention as a potential treatment for a wide range of immune-mediated and degenerative diseases. The therapeutic effects of MSCs are primarily mediated through paracrine signaling and secretion of cytokines that regulate immune responses and promote tissue repair. This review focuses on five key cytokines involved in MSC immunomodulation: interleukin-6 (IL-6), interleukin-10 (IL-10), transforming growth factor-beta (TGF-β), tumor necrosis factor-alpha (TNF-α), and interleukin-1 beta (IL-1β). These cytokines interact within a complex signaling network that allows MSCs to suppress excessive inflammation and restore immune balance. The role of MSC therapy is examined in several clinically relevant conditions, including systemic lupus erythematosus, systemic sclerosis, ischemic stroke, spinal cord injury, diabetes mellitus, and female infertility. Across these diseases, MSCs demonstrate the ability to inhibit pro-inflammatory immune cell activity, promote regulatory immune phenotypes, reduce oxidative stress, and stimulate regeneration through the secretion of growth factors and extracellular vesicles. Despite promising experimental and early clinical findings, several limitations remain, including variability in MSC sources, limited cell survival after transplantation, and the need for optimized dosing strategies. Overall, MSC therapy represents a multifunctional therapeutic approach combining immunomodulation, anti-inflammatory activity, and regenerative support. Further research is required to better understand cytokine interactions, improve standardization of MSC-based treatments, and enhance clinical efficacy across diverse pathological conditions.

Background/Objectives: Radon is a naturally occurring radioactive gas and the leading source of natural radiation exposure worldwide; however, its systemic biological effects in children remain poorly understood. This study examined the association between cumulative indoor radon exposure and inflammatory biomarkers among children residing in rural communities of the Aqmola region in Kazakhstan. Methods: The study included 87 children and adolescents (42 exposed and 45 controls). Radon exposure was measured in residential and school environments, and a composite Radon Exposure Index (REI) was constructed to estimate cumulative exposure over time. Serum concentrations of inflammatory biomarkers, including C-reactive protein (CRP), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), interleukin-6 (IL-6), and interleukin-8 (IL-8), were measured using validated immunoassay methods. Multivariable linear regression models adjusted for age, sex, body mass index, pubertal development stage, and heating type were used to evaluate associations between REI and biomarker levels. Results: Children and adolescents living in the radon-exposed community had significantly higher REI values than controls (7.75 ± 0.85 vs.4.83 ± 0.41, respectively). Among the biomarkers examined, CRP, TNF-α, IL-1β, IL-8 and IL-6 were not significantly associated with radon exposure. Conclusions: These findings do not support the use of the evaluated inflammatory biomarkers as indicators of early biological effects of environmental radon exposure in this population. However, the clear exposure contrast observed between study settings underscores the ongoing public health relevance of radon as an environmental hazard. Continued efforts to monitor and mitigate radon exposure in high-risk regions remain essential, particularly in environments where children spend substantial amounts of time.