Publications by authors named "Simone Lasagni"

Article Synopsis
  • The study analyzed the relationship between the neoangiogenic transcriptomic signature (nTS) and various clinical outcomes in patients with hepatocellular carcinoma (HCC), involving a large cohort of 584 patients.
  • Findings showed that nTS is linked to more aggressive disease characteristics, limited treatment options, and poorer overall survival compared to those without nTS, with significant consequences on treatment effectiveness and patient prognosis.
  • Repeated transarterial chemoembolization (TACE) was found to convert some patients from nTS- to nTS+, which correlated with worsened survival rates and changes in microRNA patterns, emphasizing the nTS's role in managing and predicting HCC outcomes.
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Hepatocellular carcinoma (HCC) is the second leading cause of cancer death worldwide. Curative treatments are available to a minority of patients, as HCC is often diagnosed at an advanced stage. For patients with unresectable and multifocal HCC, tyrosine kinase inhibitor drugs (TKIs) are the only potential treatment option.

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Background And Aim: VETC (vessel that encapsulate tumor cluster) is a peculiar vascular phenotype observed in hepatocellular carcinoma (HCC), associated with distant metastases and poor outcome. VETC has been linked to the Tie2/Ang2 axis and is characterized by lymphocytes poor (cold) tumor microenvironment (TME). In this setting the role of Tumor Associated Macrophages (TAMs) has never been explored.

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Aggressive hepatocellular carcinoma (HCC) overexpressing Angiopoietin-2 (ANG-2) (a protein linked with angiogenesis, proliferation, and epithelial-mesenchymal transition (EMT)), shares 95% of up-regulated genes and a similar poor prognosis with the proliferative subgroup of intrahepatic cholangiocarcinoma (iCCA). We analyzed the pro-invasive effect of ANG-2 and its regulator vascular endothelial growth factor (VEGF) on HCC and CCA spheroids to uncover posUsible common ways of response. Four cell lines were used: Hep3B and HepG2 (HCC), HuCC-T1 (iCCA), and EGI-1 (extrahepatic CCA).

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Article Synopsis
  • Patients with liver cirrhosis should undergo regular surveillance using ultrasound and α-fetoprotein testing to detect hepatocellular carcinoma (HCC) early.
  • A 12-year study compared various scoring systems, finding that the GALAD score outperformed others in predicting HCC development in patients with chronic liver disease.
  • Ultimately, the study concluded that GALAD is the most accurate system for assessing HCC risk, particularly in patients with different liver disease etiologies, including those related to alcohol.
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We evaluated SARS-CoV-2 antibody response in voluntary blood donors in Italy at different timepoints. Immediately after lockdown easing, 908/25,657 donors (3.5%) had low IgG titers against nucleocapsid.

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The male/female ratio of patients with hepatocellular carcinoma (HCC) is often unbalanced towards the male sex, indicating a sex predisposition for HCC development. A possible explanation may be attributed to different hormonal statuses, including the pro-inflammatory action of androgens in men and the protective effects of oestrogen against excessive inflammation in women. Although several studies have studied gene expression in patients with HCC, very few have attempted to identify features that could be distinctive between male and female patients.

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Background: Though the precise criteria for accessing LT are consistently being applied, HCC recurrence (HCC-R_LT) still affects more than 15% of the patients. We analyzed the clinical, histopathological, and biological features of patients with HCC to identify the predictive factors associated with cancer recurrence and survival after LT.

Methods: We retrospectively analyzed 441 patients with HCC who underwent LT in our center.

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This study examined the association between dynamic angiopoietin-2 assessment and COVID-19 short- and long-term clinical course. We included consecutive hospitalized patients from 1 February to 31 May 2020 with laboratory-confirmed COVID-19 from 2 Italian tertiary referral centers (derivation cohort, n = 187 patients; validation cohort, n = 62 patients). Serum biomarker levels were measured by sandwich enzyme-linked immunosorbent assay.

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