Institution
University of Palermo
Education•Palermo, Italy•
About: University of Palermo is a education organization based out in Palermo, Italy. It is known for research contribution in the topics: Population & Medicine. The organization has 15621 authors who have published 40250 publications receiving 964384 citations. The organization is also known as: Università degli Studi di Palermo & Universita degli Studi di Palermo.
Topics: Population, Medicine, Cancer, Context (language use), Catalysis
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TL;DR: The results showed that agricultural management influenced water and sediment dynamics and that tillage and herbicide treatment should be avoided.
348 citations
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TL;DR: What is known about movement of such particles in soil, which players and factors could influence this, and avenues for research aimed at the movement and distribution of microplastic in agricultural soils are sketched.
Abstract: We live in a plastic age (Thompson et al., 2009), with microplastic (typically defined as plastic particles < 5mm) becoming an increasingly appreciated aspect of environmental pollution. Research has been overwhelmingly focused on aquatic systems, especially the oceans, but there is a current shift to more strongly consider terrestrial ecosystems (Rillig, 2012; Horton et al., 2017). In particular agroecosystems are coming into focus as a major entry point for microplastics in continental systems (Nizzetto et al., 2016b), where contamination might occur via different sources as sludge amendment or plastic mulching (Steinmetz et al., 2016). Given the central role of agroecosystems, including their soil biodiversity (Rillig et al., 2016), in food production, such numbers are potential cause for concern. Field data on measured microplastic presence in agricultural soils are still not widely available, but nevertheless this material is certain to arrive at the soil surface. The fate of material deposited at the soil surface is not clear: particles may be removed by wind or water erosion, becoming airborne, or may be lost by surface runoff (Nizzetto et al., 2016a). Nevertheless, a substantial part of the microplastic (or nanoplastic following further disintegration) is expected to enter the soil. The degree of hazard represented by microplastic to various soil biota is not clear. Direct evidence comes from experimental work on earthworms, on which microbeads had negative effects (Huerta Lwanga et al., 2016; also reviewed in Horton et al., 2017). Data on impacts on other soil biota groups are not available. However, Kiyama et al. (2012) have shown that polystyrene beads can be taken up by the nematode Caenorhabditis elegans; this means the material could also accumulate in the soil food web (Rillig, 2012). Movement into soil is an important aspect of assessing risk: will soil biota be exposed to microplastics? Here, we sketch what is known about movement of such particles in soil, which players and factors could influence this, and we chart avenues for research aimed at the movement and distribution of microplastic in agricultural soils.
348 citations
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TL;DR: The analysis of CSCs may predict the survival of glioblastoma patients and in vitro CSC generation and presence of CD133+/Ki67+ cells are two considerable prognostic factors of disease progression and poor clinical outcome.
Abstract: Purpose: Cancer stem cells (CSC) are thought to represent the population of tumorigenic cells responsible for tumor development. The stem cell antigen CD133 identifies such a tumorigenic population in a subset of glioblastoma patients. We conducted a prospective study to explore the prognostic potential of CSC analysis in glioblastoma patients. Experimental Design: We investigated the relationship between the in vitro growth potential of glioblastoma CSCs and patient death or disease progression in tumors of 44 consecutive glioblastoma patients treated with complete or partial tumorectomy followed by radiotherapy combined with temozolomide treatment. Moreover, we evaluated by immunohistochemistry and immunofluorescence the prognostic value of the relative presence of CD133 + and CD133 + /Ki67 + cells in patient tumors. Results: In vitro CSC generation and the presence of ≥2% CD133 + cells in tumor lesions negatively correlated with overall ( P = 0.0001 and 0.02, respectively) and progression-free ( P = 0.0002 and 0.01, respectively) survival of patients. A very poor overall ( P = 0.007) and progression-free ( P = 0.001) survival was observed among patients whose tumors contained CD133 + cells expressing Ki67. Taking into account symptom duration, surgery type, age, O 6 -methylguanine-DNA methyltransferase promoter methylation, and p53 status, generation of CSCs and CD133/Ki67 coexpression emerged as highly significant independent prognostic factors, with an adjusted hazard ratio of 2.92 (95% confidence interval, 1.37-6.2; P = 0.005) and 4.48 (95% confidence interval, 1.68-11.9; P = 0.003), respectively. Conclusions: The analysis of CSCs may predict the survival of glioblastoma patients. In vitro CSC generation and presence of CD133 + /Ki67 + cells are two considerable prognostic factors of disease progression and poor clinical outcome.
346 citations
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TL;DR: Hepatitis C virus infection acts independently of HBV infection (another risk factor) and of alcohol abuse, age, or gender and is a risk factor for hepatocellular carcinoma, apparently by inducing Cirrhosis and, to a lesser extent, by enhancing the risk in patients with cirrhosis.
Abstract: Objective To determine whether chronic hepatitis C virus (HCV) infection is an independent risk factor for hepatocellular carcinoma and whether it increases the cirrhosis-related risk for hepatocellular carcinoma. Design Two pair-matched case-control studies. Setting A referral-based hospital. Patients In study I, 212 patients with hepatocellular carcinoma (197 of whom had known underlying cirrhosis) were compared with controls who had chronic nonhepatic diseases. In study II, the 197 patients with hepatocellular carcinoma and cirrhosis were compared with 197 pair-matched controls who had cirrhosis but not hepatocellular carcinoma. Measurements Levels of antibody to HCV (anti-HCV), hepatitis B surface antigen (HBsAg), and antibody to hepatitis B core antigen (anti-HBc) were assayed, and alcohol abuse was assessed by history. Main results In study I, 151 patients (71%) with hepatocellular carcinoma were anti-HCV positive compared with 11 controls (5%) with chronic nonhepatic diseases (odds ratio, 42; 95% CI, 22 to 95). Multivariate analysis showed that anti-HCV was an independent risk factor for hepatocellular carcinoma (odds ratio, 69; CI, 15 to 308). The analysis also showed that HBsAg (odds ratio, 8.7; CI, 1.5 to 50) and anti-HBc (odds ratio, 4.2 (CI, 1.7 to 11) were risk factors for hepatocellular carcinoma. No statistically significant interaction was found between anti-HCV and the markers of HBV infection. In study II, 146 patients (74%) with hepatocellular carcinoma and cirrhosis were anti-HCV positive compared with 122 patients (62%) with cirrhosis alone (odds ratio, 1.8; CI, 1.1 to 2.8). Multivariate analysis confirmed that anti-HCV (odds ratio, 2.0; CI, 1.3 to 32) and HBsAg (odds ratio, 2.0; CI, 1.0 to 4.2) were independent risk factors for hepatocellular carcinoma. Conclusions Hepatitis C virus infection is a risk factor for hepatocellular carcinoma, apparently by inducing cirrhosis and, to a lesser extent, by enhancing the risk in patients with cirrhosis. Hepatitis C virus infection acts independently of HBV infection (another risk factor) and of alcohol abuse, age, or gender.
345 citations
Authors
Showing all 15895 results
Name | H-index | Papers | Citations |
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Robin M. Murray | 171 | 1539 | 116362 |
Frede Blaabjerg | 147 | 2161 | 112017 |
Jean Bousquet | 145 | 1288 | 96769 |
Zhanhu Guo | 128 | 886 | 53378 |
Jean Ballet | 115 | 263 | 46301 |
Antonio Facchetti | 111 | 602 | 51885 |
Michele Pagano | 97 | 306 | 42211 |
Frank Z. Stanczyk | 93 | 620 | 30244 |
Eleonora Troja | 91 | 271 | 30873 |
Francesco Sciortino | 90 | 536 | 28956 |
Zev Rosenwaks | 89 | 772 | 32039 |
Antonio Russo | 88 | 934 | 34563 |
Carlo Salvarani | 88 | 730 | 31699 |
Giuseppe Basso | 87 | 643 | 33320 |
Antonio Craxì | 86 | 659 | 39463 |