45 research outputs found

    Acute myelogenous leukemia switch lineage upon relapse to acute lymphoblastic leukemia: a case report

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    Acute leukemia, the most common form of cancer in children, accounts for approximately 30% of all childhood malignancies, with acute lymphoblastic leukemia being five times more frequent than acute myeloid leukemia. Lineage switch is the term that has been used to describe the phenomenon of acute leukemias that meet the standard French-American-British system criteria for a particular lineage (either lymphoid or myeloid) upon initial diagnosis, but meet the criteria for the opposite lineage at relapse. Many reports have documented conversions of acute lymphoblastic leukemia to acute myeloid leukemia

    Multi-Scale Modeling of HIV Infection in vitro and APOBEC3G-Based Anti-Retroviral Therapy

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    The human APOBEC3G is an innate restriction factor that, in the absence of Vif, restricts HIV-1 replication by inducing excessive deamination of cytidine residues in nascent reverse transcripts and inhibiting reverse transcription and integration. To shed light on impact of A3G-Vif interactions on HIV replication, we developed a multi-scale computational system consisting of intracellular (single-cell), cellular and extracellular (multicellular) events by using ordinary differential equations. The single-cell model describes molecular-level events within individual cells (such as production and degradation of host and viral proteins, and assembly and release of new virions), whereas the multicellular model describes the viral dynamics and multiple cycles of infection within a population of cells. We estimated the model parameters either directly from previously published experimental data or by running simulations to find the optimum values. We validated our integrated model by reproducing the results of in vitro T cell culture experiments. Crucially, both downstream effects of A3G (hypermutation and reduction of viral burst size) were necessary to replicate the experimental results in silico. We also used the model to study anti-HIV capability of several possible therapeutic strategies including: an antibody to Vif; upregulation of A3G; and mutated forms of A3G. According to our simulations, A3G with a mutated Vif binding site is predicted to be significantly more effective than other molecules at the same dose. Ultimately, we performed sensitivity analysis to identify important model parameters. The results showed that the timing of particle formation and virus release had the highest impacts on HIV replication. The model also predicted that the degradation of A3G by Vif is not a crucial step in HIV pathogenesis

    Analysis of radiopacity, pH and cytotoxicity of a new bioceramic material

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    AbstractObjective RetroMTA® is a new hydraulic bioceramic indicated for pulp capping, perforations or root resorption repair, apexification and apical surgery. The aim of this study was to compare the radiopacity, pH variation and cytotoxicity of this material to ProRoot® MTA.Material and Methods Mixed cements were exposed to a digital x-ray along with an aluminum stepwedge for the radiopacity assay. pH values were verified after incubation period of 3, 24, 48, 72 and 168 hours. The cytotoxicity of each cement was tested on human periodontal ligament fibroblasts using a multiparametric assay. Data analysis was performed using ANOVA and Tukey’spost hoc in GraphPad Prism.Results ProRoot® MTA had higher radiopacity than RetroMTA®(p0.05) although pH levels of both materials reduced over time. Both ProRoot® MTA and RetroMTA® allowed for significantly higher cell viability when compared with the positive control (p<0.001). No statistical difference was observed between ProRoot® MTA and RetroMTA® cytotoxicity level in all test parameters, except for the ProRoot® MTA 48-hour extract media in the NR assay (p<0.05).Conclusion The current study provides new data about the physicochemical and biological properties of Retro® MTA concerning radiopacity, pH and cytotoxic effects on human periodontal ligaments cells. Based on our findings, RetroMTA® meets the radiopacity requirements standardized by ANSI/ADA number 572, and similar pH values and biocompatibility to ProRoot® MTA. Further studies should be performed to evaluate additional properties of this new material

    Platelet membrane studies in the May-Hegglin anomaly

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    Histopathological Study of Periapical Inflammation Following Preparation of the Root Canal with Conventional and Profile Rotary Instrumentation in Teeth of Cats

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    Statement of Problem: Various factors are involved in causing inflammation following root canal treatment. Controlling these factors may relieve the related pain. One of these factors is extrusion of debris beyond the apex. Although debris extrusion happens in all instrumentation techniques, researchers have declared that in coronal flaring technique,there is minimum debris extrusion.Purpose: The purpose of this study was to evaluate and compare the inflammation of periapical area following root canal therapy, using conventional and profile rotary instrumentation in cats' teeth, from a histopathological point of view.Materials and Methods: This experimental study conducted on thirty Persian one year old cats. Three groups of samples were chosen and treated with different methods. First group were prepared by step-back instrumentation technique using stainless steel Ktypefiles. Second group were prepared by crown down technique using Ni-Ti files.Third group were prepared using profile GT rotary system at 150-rpm speed. Animals were subjected to vital perfusion at 8, 24 & 48 hour intervals after instrumentation. The canine teeth were separated from the jaw along with some of the supporting structures.Then decalcification and laboratory processing were carried out and samples were evaluated histologically. Collected data were analyzed using Kruskal-Wallis test.Results: The results showed that in vital teeth with no evidence of periapical pathosis,the inflammation following various instrumentation methods was not statistically different.Conclusion: In vital teeth, the periapical inflammation following various methods of instrumentation is not statistically different

    Histologic evaluation of repair of mechanical furcal perforations in dog premolars, using gray MTA, white MTA &amp; Portland cement

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    Background and Aim: Furcal perforation has a great impact on prognosis of endodontic treatments, requiring immediate and proper intervention. Gray MTA is applied as material of choice in repairing perforations. The aim of this study was to evaluate the repair of mechanical furcal perforations, histologically using white MTA and Portland cement and compare them with gray MTA. Materials and Methods: In this experimental study, second to fourth mandibular and maxillary premolar teeth of five dogs received endodontic treatment, then the furcation area of the teeth were perforated and repaired as follow: gray MTA in group1, white MTA in group 2, Portland cement in group 3 and cotton pellet in group 4 (control). Animals were controlled for 4 months and sacrificed using an over dosage of sodium thiopental intravenous injection and perfusion of 10% formaldehyde. Chi-square and Fisher exact tests were used to compare hard tissue formation between groups and between each two groups, respectively. Non-parametric Kruskall Wallis and Dunn procedure were also used to compare degree of inflammation among groups and between each two groups, respectively. Results: Gray MTA had more favorable results (90.9% hard tissue formation and only 9.1% severe inflammation) but the difference between gray MTA, white MTA and Portland cement was not statistically significant. Conclusion: The difference between gray MTA, white MTA and Portland cement groups was not statistically significant for degree of inflammation and hard tissue formation. In conclusion both white MTA and Portland cement can be used instead of gray MTA to repair perforations in accordance to esthetic considerations

    COLORECTAL CARCINOMA AND LYMPHOMA

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    Targeting autophagy in prostate cancer: preclinical and clinical evidence for therapeutic response

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    10.1186/s13046-022-02293-6Journal of Experimental and Clinical Cancer Research411105
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