Publications by authors named "Caporossi D"

Unlabelled: This study examines how power training affects estimated bone strength, revealing that females benefit more than males, especially in the upper limbs (radius). These findings highlight the importance of designing sex-specific exercise programs to enhance bone health. Further research is needed to optimize training duration and address site-specific differences.

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  • Breast cancer (BC) is a major global health issue for women, and studies show that physical activity (PA) can significantly improve quality of life, recovery, and survival rates in BC patients.
  • PA affects DNA methylation, potentially reversing abnormal patterns linked to cancer and other diseases, and this review highlights how PA influences both global and gene-specific DNA methylation in BC patients.
  • The analysis indicates that PA can elevate global DNA methylation in tumors and affects various genes associated with important biological processes, underscoring its potential to restore normal cell function and improve recovery and survival outcomes for BC patients.
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  • - Biological age is a more accurate reflection of health than chronological age, and a study shows that a 16-week online physical activity program can significantly reduce biological age in breast cancer survivors post-surgery.
  • - Although telomere length remained unchanged, the ELOVL2 epigenetic clock indicated that participants in the physical activity group experienced a reduction in biological age, linked to improvements in cardiovascular fitness and strength.
  • - The study suggests that incorporating physical activity can support better recovery for breast cancer patients and highlights the potential of epigenetic clocks as a tool to assess health status and identify at-risk individuals.
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The evidence for physical activity (PA) as a major public health preventive approach and a potent medical therapy has increased exponentially in the last decades. The biomolecular mechanisms supporting the associations between PA and/or structured exercise training with health maintenance and disease prevention are not completely characterized. However, increasing evidence pointed out the role of epigenetic modifications in exercise adaptation and health-enhancing PA throughout life, DNA methylation being the most intensely studied epigenetic modification induced by acute and chronic exercise.

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Most anticancer treatments act on oxidative-stress pathways by producing reactive oxygen species (ROS) to kill cancer cells, commonly resulting in consequential drug-induced systemic cytotoxicity. Physical activity (PA) has arisen as an integrative cancer therapy, having positive health effects, including in redox-homeostasis. Here, we investigated the impact of an online supervised PA program on promoter-specific DNA methylation, and corresponding gene expression/activity, in 3 antioxidants- (SOD1, SOD2, and CAT) and 3 breast cancer (BC)-related genes (BRCA1, L3MBTL1 and RASSF1A) in a population-based sample of women diagnosed with primary BC, undergoing medical treatment.

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  • Breast cancer (BC) treatment
  • : The study focuses on how physical activity (PA) can help manage oxidative stress and inflammation in women who have had surgery for breast cancer. It suggests PA can help counteract the negative effects of medical treatment.
  • Health benefits
  • : Results show that PA maintains important antioxidant levels and reduces inflammation markers, while also improving physical fitness, body composition, and overall quality of life (QoL) for post-surgery patients.
  • Impact of PA
  • : The research indicates that a tailored PA program enhances functional capabilities, reduces fatigue, and promotes beneficial cellular responses, all of which can contribute positively to the recovery of breast cancer patients undergoing additional treatment.
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Cardiovascular diseases (CVD) can cause various conditions, including an increase in reactive oxygen species (ROS) levels that can decrease nitric oxide (NO) availability and promote vasoconstriction, leading to arterial hypertension. Physical exercise (PE) has been found to be protective against CVD by helping to maintain redox homeostasis through a decrease in ROS levels, achieved by increased expression of antioxidant enzymes (AOEs) and modulation of heat shock proteins (HSPs). Extracellular vesicles (EVs) circulating in the body are a major source of regulatory signals, including proteins and nucleic acids.

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Considering the role of redox homeostasis in exercise-induced signaling and adaptation, this study focuses on the exercise training-related intercellular communication of redox status mediated by circulating extracellular vesicles (EVs). 19 healthy young males were divided into trained (TG, 7) and untrained (UG, 12) subjects based on their VO. The UG subjects were further randomly distributed in experimental (UG, N = 7) and control (UG, N = 5) groups.

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  • The study investigates how physical activity (PA) habits before and after a diagnosis of systemic sclerosis (SSc) affect disease activity and progression among patients.
  • It analyzes self-reported data from 34 adult patients, focusing on various demographic and health-related parameters, including disease duration and quality of life.
  • Findings indicate that higher levels of physical activity prior to diagnosis are associated with better health outcomes, such as shorter disease duration and lower pulmonary pressure in certain SSc subtypes.
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  • Skeletal muscle can produce androgens, but the impact of reactive oxygen species (ROS) on this process in muscle cells remains unexplored compared to its effects on reproductive cells.
  • The study aimed to see how mild ROS exposure, using hydrogen peroxide, affects the release of testosterone (T) and dihydrotestosterone (DHT) in mouse muscle cells, along with the expression of important enzymes related to steroid production.
  • Results indicated that hydrogen peroxide increased DHT release and affected steroidogenic enzyme expression, while tadalafil, a drug often misused for performance enhancement, reduced DHT release triggered by hydrogen peroxide.
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The increase in breast cancer (BC) survival has determined a growing survivor population that seems to develop several comorbidities and, specifically, treatment-induced cardiovascular disease (CVD), especially those patients treated with anthracyclines. Indeed, it is known that these compounds act through the induction of supraphysiological production of reactive oxygen species (ROS), which appear to be central mediators of numerous direct and indirect cardiac adverse consequences. Evidence suggests that physical exercise (PE) practised before, during or after BC treatments could represent a viable non-pharmacological strategy as it increases heart tolerance against many cardiotoxic agents, and therefore improves several functional, subclinical, and clinical parameters.

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HSPB5 or alpha B-crystallin (CRYAB), originally identified as lens protein, is one of the most widespread and represented of the human small heat shock proteins (sHSPs). It is greatly expressed in tissue with high rates of oxidative metabolism, such as skeletal and cardiac muscles, where HSPB5 dysfunction is associated with a plethora of human diseases. Since HSPB5 has a major role in protecting muscle tissues from the alterations of protein stability (i.

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Regular physical activity can enhance immune function and effectively prevents the spread of the cytokine response, thus reducing systemic low-grade inflammation and improving various immune markers. Moreover, regular exercise maintains redox homeostasis in skeletal muscle and other tissues, including immune cells, but the interconnection between the anti-inflammatory effects of exercise with the redox status of immune cells is still poorly understood. With the aim to verify the overall beneficial effect of regular training on the immune system, we have examined the acute and short-term effect of a 5-day exercise program on the modulation of protein and lipid oxidation, antioxidants (i.

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Breast cancer (BC) is the most commonly diagnosed cancer among women worldwide and the most common cause of cancer-related death. To date, it is still a challenge to estimate the magnitude of the clinical impact of physical activity () on those parameters producing significative changes in future BC risk and disease progression. However, studies conducted in recent years highlight the role of not only as a protective factor for the development of ER+ breast cancer but, more generally, as a useful tool in the management of BC treatment as an adjuvant to traditional therapies.

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Oxidative stress plays a key role in systemic sclerosis (SSc) pathogenesis, and an altered redox homeostasis might be responsible for abnormal inflammatory status, fibrosis and tissue damage extension. In this study, we explored the effect of the phosphodiesterase type 5 inhibitor sildenafil in modulating the activation of the CXCL-9, -10, -11/CXCR3 axis, which is fundamental in the perpetuation of inflammation in different autoimmune diseases, in the cell culture of SSc human dermal fibroblasts exposed to a pro-oxidant environment. We observed that sildenafil significantly reduced gene expression and release of CXCL-9, -10 and -11, inhibited the CXCR3 action and suppressed the activation of STAT1-, JNK- and p38MAPK pathways.

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Skeletal muscle is a plastic and complex tissue, rich in proteins that are subject to continuous rearrangements. Skeletal muscle homeostasis can be affected by different types of stresses, including physical activity, a physiological stressor able to stimulate a robust increase in different heat shock proteins (HSPs). The modulation of these proteins appears to be fundamental in facilitating the cellular remodeling processes related to the phenomenon of training adaptations such as hypertrophy, increased oxidative capacity, and mitochondrial activity.

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To date, there are limited and incomplete data on possible sex-based differences in fiber-types of skeletal muscle and their response to physical exercise. Adult healthy male and female mice completed a single bout of endurance exercise to examine the sex-based differences of the peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC1α), heat shock protein 60 (Hsp60), interleukin 6 (IL-6) expression, as well as the Myosin Heavy Chain (MHC) fiber-type distribution in soleus and extensor digitorum longus (EDL) muscles. Our results showed for the first time that in male soleus, a muscle rich of type IIa fibers, endurance exercise activates specifically genes involved in mitochondrial biogenesis such as PGC1 α1 isoform, Hsp60 and IL-6, whereas the expression of PGC1 α2 and α3 was significantly upregulated in EDL muscle, a fast-twitch skeletal muscle, independently from the gender.

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AlphaB-crystallin (HSPB5) is one of the most prominent and well-studied members of the small heat shock protein (sHsp) family. To date, it is known that this protein modulates significant cellular processes and therefore, it is not surprising that its deregulation is involved in various human pathologies, including cancer diseases. Despite the pathogenic significance of HSPB5 in cancer and its regulatory mechanism related to aggressiveness is poorly understood, several reports describe the association of breast carcinoma progression with HSPB5, whose expression is also considered an independent predictor of breast cancer metastasis to the brain.

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  • * Sildenafil, a drug that inhibits phosphodiesterase type 5, shows promise in protecting cells from damage caused by reactive oxygen species (ROS), which are linked to oxidative stress.
  • * The study found that SSc fibroblasts are more sensitive to oxidative harm, but sildenafil treatment reduced DNA damage, improved cell viability, and supported maintenance of cellular redox balance, suggesting its potential as a therapeutic option for SSc.
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Long non-coding RNAs (lncRNAs) play critical roles in various biological functions and disease processes including cancer. The metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) was initially identified as a lncRNA with elevated expression in primary human non-small cell lung tumors with high propensity to metastasize, and subsequently shown to be highly expressed in numerous other human cancers including breast, ovarian, prostate, cervical, endometrial, gastric, pancreatic, sarcoma, colorectal, bladder, brain, multiple myeloma, and lymphoma. MALAT1 is deeply involved in several physiological processes, including alternative splicing, epigenetic modification of gene expression, cellular senescence, healthy aging, and redox homeostasis.

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RNA-binding proteins orchestrate the composite life of RNA molecules and impact most physiological processes, thus underlying complex phenotypes. The RNA-binding protein Sam68 regulates differentiation processes by modulating splicing, polyadenylation, and stability of select transcripts. Herein, we found that mice display altered regulation of alternative splicing in the spinal cord of key target genes involved in synaptic functions.

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  • Oxidative stress is linked to vascular damage and plays a significant role in the development of systemic sclerosis (SSc), particularly in patients with Raynaud's Phenomenon (RP).
  • In this study, the effects of sildenafil, a phosphodiesterase type 5 inhibitor used for RP, were analyzed on human fibroblasts, showing that it reduces inflammation markers (IL-6 and IL-8) when exposed to reactive oxygen species.
  • The reduction in these markers was connected to the suppression of key cellular pathways and suggests that sildenafil might help prevent tissue damage in SSc by modulating pro-inflammatory responses.
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The αB-crystallin (HSPB5) protein is modulated in response to a wide variety of stressors generated by multiple physio-pathological conditions, sustained by reactive oxygen species (ROS) production. In cardiac muscle tissue, this protein regulates various cellular processes, such as protein degradation, apoptosis and the stabilization of cytoskeletal elements. In this work, we studied the role of HSPB5 expression, activation and localization in HL-1 murine cardiomyocytes exposed to pro-oxidant and non-cytotoxic HO concentration, as well as in cardiac tissue isolated from mice following an acute, non-damaging endurance exercise.

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Physical exercise represents one of the strongest physiological stimuli capable to induce functional and structural modifications in all biological systems. Indeed, beside the traditional genetic mechanisms, physical exercise can modulate gene expression through epigenetic modifications, namely DNA methylation, post-translational histone modification and non-coding RNA transcripts. Initially considered as merely damaging molecules, it is now well recognized that both reactive oxygen (ROS) and nitrogen species (RNS) produced under voluntary exercise play an important role as regulatory mediators in signaling processes.

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