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71.
Federica Cipriani Mohammad Alzoubi David Fuks Francesca Ratti Takayuki Kawai Giammauro Berardi Leonid Barkhatov Panagiotis Lainas Marcel Van der Poel Morad Faoury Marc G. Besselink Mathieu DHondt Ibrahim Dagher Bjorn Edwin Roberto Ivan Troisi Olivier Scatton Brice Gayet Luca Aldrighetti Mohammad Abu Hilal 《Journal of hepato-biliary-pancreatic sciences》2020,27(1):3-15
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Federica Fusella Roberta Ferretti Daniele Recupero Stefania Rocca Augusta Di Savino Giusy Tornillo Lorenzo Silengo Emilia Turco Sara Cabodi Paolo Provero Pier Paolo Pandolfi Anna Sapino Guido Tarone Mara Brancaccio 《The Journal of pathology》2014,234(2):152-163
Morgana/CHP‐1 is a ubiquitously expressed protein able to inhibit ROCK II kinase activity. We have previously demonstrated that morgana haploinsufficiency leads to multiple centrosomes, genomic instability, and higher susceptibility to tumour development. While a large fraction of human cancers has shown morgana down‐regulation, a small subset of tumours was shown to express high morgana levels. Here we demonstrate that high morgana expression in different breast cancer subtypes correlates with high tumour grade, mitosis number, and lymph node positivity. Moreover, morgana overexpression induces transformation in NIH‐3T3 cells and strongly protects them from various apoptotic stimuli. From a mechanistic point of view, we demonstrate that morgana causes PTEN destabilization, by inhibiting ROCK activity, hence triggering the PI3K/AKT survival pathway. In turn, morgana down‐regulation in breast cancer cells that express high morgana levels increases PTEN expression and leads to sensitization of cells to chemotherapy. Copyright © 2014 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd 相似文献
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Robert A. Power Sarah Cohen‐Woods Mandy Y. Ng Amy W. Butler Nick Craddock Ania Korszun Lisa Jones Ian Jones Michael Gill John P. Rice Wolfgang Maier Astrid Zobel Ole Mors Anna Placentino Marcella Rietschel Katherine J. Aitchison Federica Tozzi Pierandrea Muglia Gerome Breen Anne E. Farmer Peter McGuffin Cathryn M. Lewis Rudolf Uher 《American journal of medical genetics. Part B, Neuropsychiatric genetics》2013,162(6):521-529
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Antonio Bellasi Stefano Zona Gabriella Orlando Federica Carli Guido Ligabue Vincenzo Rochira Antonella Santoro Cristina Mussini Giovanni Guaraldi Paolo Raggi 《Calcified tissue international》2013,93(5):413-418
HIV-infected individuals suffer from accelerated aging, which manifests as premature cardiovascular and bone disease. However, little is known of the association of these two disorders in the HIV population. Our objective was to investigate the association between a marker of atherosclerosis (coronary artery calcium [CAC]) and low bone mineral density (BMD) in a cross-sectional cohort of HIV-infected patients. The study was conducted at the University of Modena and Reggio Emilia, Italy. A total of 636 consecutive middle-aged, HIV-infected subjects were recruited between January 2006 and December 2010. All patients underwent CAC and BMD assessment. Patients were categorized according to a CAC score <100 or >100 units based on previous literature that identified this cut-point as a marker of increased risk. Low femoral and lumbar spine BMD was defined as <25th percentile value for the study cohort. Logistic regression and bootstrap analysis were used to assess the independent association between CAC and BMD. The main outcome measure was a CAC score >100. Patients with CAC > 100 were older and more likely to be men, diabetic, and overweight. Patients with CAC < 100 had better renal function and a lower cardiovascular risk profile. After adjusting for age, sex, traditional and HIV-specific risk factors, vitamin D level, and PTH level, there was a significant association between CAC > 100 and low BMD for the femur (OR = 2.33, 95 % CI 1.09–4.99; p = 0.02) but not for the spine. Bootstrap analyses confirmed these findings. In summary, CAC was independently associated with low femoral BMD in HIV-infected patients. Future studies should test whether therapies that attenuate cardiovascular risk in HIV favorably impact bone health. 相似文献
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Tomao F Di Tucci C Marchetti C Perniola G Bellati F Panici PB 《Critical reviews in oncology/hematology》2012,82(1):25-39
The aim of this review is to evaluate the use of chemotherapy (CT) in the treatment of squamous vulvar cancer. Since the 90s there was a continuous evolution in the therapeutic approach to this tumour. Although primary surgery is now considered the most effective approach, there are advanced diseases in which surgery may compromise anatomical structures causing severe mutilation. These are the reasons why CHT, with or without concomitant radiotherapy RT, started to be strongly recommended as neoadjuvant strategy. Chemotherapeutic agents have also been used alone as adjuvant treatment or in association with RT, by exploiting the radiosensitizing effect of these drugs. There are few data about the use of CHT as palliative treatment but recent studies point to the use of target therapy. In conclusion, clinical data and the evidence of chemo-sensitivity in vulvar squamous cell carcinoma open new possibilities to future research in this field. 相似文献