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61.
Piaggesi A Macchiarini S Rizzo L Palumbo F Tedeschi A Nobili LA Leporati E Scire V Teobaldi I Del Prato S 《Diabetes care》2007,30(3):586-590
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Ludwig H Durie BG Bolejack V Turesson I Kyle RA Blade J Fonseca R Dimopoulos M Shimizu K San Miguel J Westin J Harousseau JL Beksac M Boccadoro M Palumbo A Barlogie B Shustik C Cavo M Greipp PR Joshua D Attal M Sonneveld P Crowley J 《Blood》2008,111(8):4039-4047
We analyzed the presenting features and survival in 1689 patients with multiple myeloma aged younger than 50 years compared with 8860 patients 50 years of age and older. Of the total 10 549 patients, 7765 received conventional therapy and 2784 received high-dose therapy. Young patients were more frequently male, had more favorable features such as low International Staging System (ISS) and Durie-Salmon stage as well as less frequently adverse prognostic factors including high C-reactive protein (CRP), low hemoglobin, increased serum creatinine, and poor performance status. Survival was significantly longer in young patients (median, 5.2 years vs 3.7 years; P < .001) both after conventional (median, 4.5 years vs 3.3 years; P < .001) or high-dose therapy (median, 7.5 years vs 5.7 years; P = .04). The 10-year survival rate was 19% after conventional therapy and 43% after high-dose therapy in young patients, and 8% and 29%, respectively, in older patients. Multivariate analysis revealed age as an independent risk factor during conventional therapy, but not after autologous transplantation. A total of 5 of the 10 independent risk factors identified for conventional therapy were also relevant for autologous transplantation. After adjusting for normal mortality, lower ISS stage and other favorable prognostic features seem to account for the significantly longer survival of young patients with multiple myeloma with age remaining a risk factor during conventional therapy. 相似文献
64.
Palumbo R Gaetano C Antonini A Pompilio G Bracco E Rönnstrand L Heldin CH Capogrossi MC 《Arteriosclerosis, thrombosis, and vascular biology》2002,22(3):405-411
In the present study, we analyzed the effect of conditioned media (CM) from bovine aortic endothelial cells exposed to laminar shear stress (SS) of 5 dyne/cm2 (SS5) or 15 dyne/cm2 (SS15) for 16 hours on smooth muscle cell (SMC) migration. In response to CM from bovine aortic endothelial cells exposed to SS5 (CMSS5) and SS15 (CMSS15), migration was 45 +/- 5.5 and 30 +/- 1.5 cells per field, respectively (P<0.05). Similar results were obtained with SS of 2 versus 20 dyne/cm2 and also when SS of 5 and 15 dyne/cm2 lasted 24 hours. Platelet-derived growth factor (PDGF)-AA levels in CMSS5 and CMSS15 were 9 +/- 7 and 18 +/- 5 ng/10(6) cells for 16 hours, respectively (P<0.05); PDGF-BB levels in CMSS5 and CMSS15 were 38 +/- 10 and 53 +/- 10 ng/10(6) cells for 16 hours, respectively (P<0.05). PDGF receptor alpha (PDGFRalpha) and PDGF receptor beta (PDGFRbeta) in SMCs were phosphorylated by CMSS15>CMSS5. In response to CMSS15, a neutralizing antibody against PDGF-AA enhanced SMC migration to a level comparable to that of CMSS5; in contrast, antibodies against PDGF-BB abolished SMC migration. Transfection of SMCs with a dominant-negative PDGFRalpha or PDGFRbeta increased or inhibited, respectively, SMC migration in response to CMSS15. Overexpression of wild-type PDGFRalpha inhibited SMC migration in response to CMSS5, CMSS15, or recombinant PDGF-BB (P<0.001). These results suggest that the ability of high SS to inhibit arterial wall thickening in vivo may be related to enhanced activation of PDGFRalpha in SMCs by PDGF isoforms secreted by the endothelium. 相似文献
65.
Barbano R ;Palumbo O ;PascuUi B ;Galasso M ;Volinia S ;D'Angelo V ;Icolaro N ;Coco M ;Dimitri L ;Graziano p ;Copetti M ;Valori VM ;Maiello E ;CareUa M ;Fazio VM ;Parrella p 《中华神经外科疾病研究杂志》2014,(5):433-433
Gliomas represent a disparate group of tumours for which there are to date no cure. Thus, there is a recognized need for new diagnostic and therapeutic approaches based on increased understanding of their molecular nature. We performed the comparison of the microRNA (miRNA) profile of 8 WHO grade II gliomas and 24 higher grade tumours (2 WHO grade III and 22 glioblastomas) by using the Affymetrix GeneChip miRNA Array v. 1.0. A relative quantification method (RT-qPCR) with standard curve was used to confirm the 22 miRNA signature resulted by array analysis. The prognostic performances of the confirmed miRNAs were estimated on the Tumor Cancer Genome Atlas (TCGA) datasets. We identified 22 miRNAs distinguishing grade II gliomas from higher grade tumours. RT-qPCR confirmed the differential expression in the two patients'groups for 13 out of the 22 miRNAs. The analysis of the Glioblastoma Multiforme (GBM) and Lower Grade Glioma (LGG) datasets from TCGA demonstrated the association with prognosis for 6 of those miRNAs. Moreover, in the GBM dataset miR-21 and miR-210 were predictors of worse prognosis in both univariable and multivariable Cox regression analyses ( HR 1.19, P = O. 04, and HR 1.18, P = 0. 029 respectively). Our results support a direct contribution of miRNAs to glioma cancerogenesis and suggest that miR-21 and miR-210 may play a role in the aggressive clinical behaviour of glioblastomas. 相似文献
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Clive M. Brown Aaron E. Aranas Gabrielle A. Benenson Gary Brunette Marty Cetron Tai-Ho Chen Nicole J. Cohen Pam Diaz Yonat Haber Christa R. Hale Kelly Holton Katrin Kohl Amanda W. Lee Gabriel J. Palumbo Kate Pearson Christina R. Phares Francisco Alvarado-Ramy Shah Roohi Lisa D. Rotz Jordan Tappero Faith M. Washburn James Watkins Nicki Pesik 《MMWR. Morbidity and mortality weekly report》2014,63(49):1163-1167
68.
TBR1 is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion 下载免费PDF全文
69.
Cognitive‐motor profile,clinical characteristics and diagnosis of CHARGE syndrome: An Italian experience 下载免费PDF全文
70.
Alexander A. Boucher Leah Rosenfeldt Duaa Mureb Jessica Shafer Bal Krishan Sharma Adam Lane Rebecca R. Crowther Melanie C. McKell Jordan Whitt Theresa Alenghat Joseph Qualls Silvio Antoniak Nigel Mackman Matthew J. Flick Kris A. Steinbrecher Joseph S. Palumbo 《Journal of thrombosis and haemostasis》2020,18(1):91-103