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  • 1
    In: Frontiers in Oncology, Frontiers Media SA, Vol. 11 ( 2021-11-16)
    Abstract: Most randomized trials for acute promyelocytic leukemia (APL) have investigated highly selected patients under idealized conditions, and the findings need to be validated in the real world. We conducted a population-based study of all APL patients in Zhejiang Province, China, with a total population of 82 million people, to assess the generalization of all-trans retinoic acid (ATRA) and arsenic as front-line treatment. The outcomes of APL patients were also analyzed. Between January 2015 and December 2019, 1,233 eligible patients were included in the final analysis. The rate of ATRA and arsenic as front-line treatment increased steadily from 66.2% in 2015 to 83.3% in 2019, with no difference among the size of the center (≥5 or & lt;5 patients per year, p = 0.12) or age (≥60 or & lt;60 years, p = 0.35). The early death (ED) rate, defined as death within 30 days after diagnosis, was 8.2%, and the 3-year overall survival (OS) was 87.9% in the whole patient population. Age (≥60 years) and white blood cell count ( & gt;10 × 10 9 /L) were independent risk factors for ED and OS in the multivariate analysis. This population-based study showed that ATRA and arsenic as front-line treatment are widely used under real-world conditions and yield a low ED rate and a high survival rate, which mimic the results from clinical trials, thereby supporting the wider application of APL guidelines in the future.
    Type of Medium: Online Resource
    ISSN: 2234-943X
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2021
    detail.hit.zdb_id: 2649216-7
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  • 2
    Online Resource
    Online Resource
    Frontiers Media SA ; 2021
    In:  Frontiers in Cell and Developmental Biology Vol. 9 ( 2021-11-5)
    In: Frontiers in Cell and Developmental Biology, Frontiers Media SA, Vol. 9 ( 2021-11-5)
    Abstract: Background: Diffuse large B-cell lymphoma (DLBCL) is a common aggressive B-cell non-Hodgkin lymphoma (B-NHL). While combined chemotherapy has improved the outcomes of DLBCL, it remains a highly detrimental disease. Pyroptosis, an inflammatory programmed cell death, is considered to have both tumor-promoting and tumor-suppressing effects. The role of pyroptosis in DLBCL has been gradually appreciated, but its value needs further investigation. Methods: We analyzed mutations and copy number variation (CNV) alterations of pyroptosis-related genes (PRGs) from The Cancer Genome Atlas (TCGA) cohort and evaluated the differences in expression in normal B cells and DLBCL patients in two Gene Expression Omnibus (GEO) datasets (GSE12195 and GSE56315). Based on the expression of 52 PRGs, we divided 421 DLBCL patients from the GSE31312 dataset into distinct clusters using consensus clustering. The Kaplan-Meier method was used to prognosis among the three clusters, and GSVA was used to explore differences in the biological functions. ESTIMATE and single-sample gene-set enrichment analysis (ssGSEA) were used to analyze the tumor immune microenvironment (TME) in different clusters. A risk score signature was developed using a univariate survival analysis and multivariate regression analysis, and the reliability and validity of the signature were verified. By combining the signature with clinical factors, a nomogram was established to predict the prognosis of DLBCL patients. The alluvial diagram and correlation matrix were used to explore the relationship between pyroptosis risk score, clinical features and TME. Results: A large proportion of PRGs are dysregulated in DLBCL and associated with the prognosis. We found three distinct pyroptosis-related clusters (cluster A, B, and C) that differed significantly with regard to the prognosis, biological process, clinical characteristics, chemotherapeutic drug sensitivity, and TME. Furthermore, we developed a risk score signature that effectively differentiates high and low-risk patients. The nomogram combining this signature with several clinical indicators showed an excellent ability to predict the prognosis of DCBCL patients. Conclusions: This work demonstrates that pyroptosis plays an important role in the diversity and complexity of the TME in DLBCL. The risk signature of pyroptosis is a promising predictive tool. A correct and comprehensive assessment of the mode of action of pyroptosis in individuals will help guide more effective treatment.
    Type of Medium: Online Resource
    ISSN: 2296-634X
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2021
    detail.hit.zdb_id: 2737824-X
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  • 3
    Online Resource
    Online Resource
    Elsevier BV ; 2017
    In:  Leukemia Research Vol. 56 ( 2017-05), p. 1-6
    In: Leukemia Research, Elsevier BV, Vol. 56 ( 2017-05), p. 1-6
    Type of Medium: Online Resource
    ISSN: 0145-2126
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2017
    detail.hit.zdb_id: 2008028-1
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  • 4
    Online Resource
    Online Resource
    Frontiers Media SA ; 2021
    In:  Frontiers in Genetics Vol. 12 ( 2021-4-26)
    In: Frontiers in Genetics, Frontiers Media SA, Vol. 12 ( 2021-4-26)
    Abstract: Multiple myeloma (MM) is a malignant hematopoietic disease that is usually incurable. RNA-binding proteins (RBPs) are involved in the development of many tumors, but their prognostic significance has not been systematically described in MM. Here, we developed a prognostic signature based on eight RBP-related genes to distinguish MM cohorts with different prognoses. Method After screening the differentially expressed RBPs, univariate Cox regression was performed to evaluate the prognostic relevance of each gene using The Cancer Genome Atlas (TCGA)-Multiple Myeloma Research Foundation (MMRF) dataset. Lasso and stepwise Cox regressions were used to establish a risk prediction model through the training set, and they were validated in three Gene Expression Omnibus (GEO) datasets. We developed a signature based on eight RBP-related genes, which could classify MM patients into high- and low-score groups. The predictive ability was evaluated using bioinformatics methods. Gene ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment, and gene set enrichment analyses were performed to identify potentially significant biological processes (BPs) in MM. Result The prognostic signature performed well in the TCGA-MMRF dataset. The signature includes eight hub genes: HNRNPC , RPLP2 , SNRPB , EXOSC8 , RARS2 , MRPS31 , ZC3H6 , and DROSHA . Kaplan–Meier survival curves showed that the prognosis of the risk status showed significant differences. A nomogram was constructed with age; B2M , LDH , and ALB levels; and risk status as prognostic parameters. Receiver operating characteristic (ROC) curve, C-index, calibration analysis, and decision curve analysis (DCA) showed that the risk module and nomogram performed well in 1, 3, 5, and 7-year overall survival (OS). Functional analysis suggested that the spliceosome pathway may be a major pathway by which RBPs are involved in myeloma development. Moreover, our signature can improve on the R-International Staging System (ISS)/ISS scoring system (especially for stage II), which may have guiding significance for the future. Conclusion We constructed and verified the 8-RBP signature, which can effectively predict the prognosis of myeloma patients, and suggested that RBPs are promising biomarkers for MM.
    Type of Medium: Online Resource
    ISSN: 1664-8021
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2021
    detail.hit.zdb_id: 2606823-0
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  • 5
    In: Japanese Journal of Infectious Diseases, Editorial Committee of Japanese Journal of Infectious Diseases, National Institute of Infectious Dis, Vol. 65, No. 3 ( 2012), p. 208-214
    Type of Medium: Online Resource
    ISSN: 1344-6304
    Language: English
    Publisher: Editorial Committee of Japanese Journal of Infectious Diseases, National Institute of Infectious Dis
    Publication Date: 2012
    detail.hit.zdb_id: 2128836-7
    SSG: 12
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  • 6
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2016-02, No. 31 ( 2016-09-01), p. 2059-2059
    Abstract: With continuous increase in transistor count and clock frequency, the power density of current Si integrated circuits has reached a level that calls for a revolutionary change in transistor technology. High hole mobility Ge and high electron mobility InGaAs have been considered to be the most promising channel materials for p-channel and n-channel MOSFETs, respectively. Selective-area growth (SAG) on nano-trenches has been quite popular in integrating III-V materials with Si substrates. Since there exists a high lattice mismatch between III-V materials and Si, obtaining defect-free epilayer is still a great challenge. In this work, we demonstrate selective area growth of InGaAs on Ge trenches aiming at integrating n-channel InGaAs FinFETs and p-channel Ge FinFETs side by side on a Si substrate for CMOS applications. The Ge templates, which were grown on Si by chemical vapor deposition, were prepared by etching through an oxide mask using a dilute H 2 O 2 solution to create Ge linear trench structures with embedded {111} facets at the bottom of the trenches for facilitating the regrowth of III-V materials. The III-V materials were selectively grown on the patterned Ge templates by metal-organic vapor phase epitaxy. An InGaP buffer layer, which has a wide bandgap and is beneficial for electrical isolation between the channel and substrate, was grown onto the Ge trenches. Undoped InGaAs was grown on InGaP as the n-channel material. High resolution transmission microscopy investigations show that very few dislocations are present near the Ge/InGaP interface in the trenches. It is found that In content of InGaP increases from 50 % to about 70 % with growth as evidenced by energy-dispersive x-ray spectroscopy (EDX). Interestingly, composition grading is also observed on the subsequently grown InGaAs. It begins from an In 0.21 Ga 0.79 As layer, which has good lattice match to the In 0.7 Ga 0.3 P layer beneath, then changes to the nominal In 0.71 Ga 0.29 As layer near the top of the fin. The strain in InGaAs is partially released through the generation of dislocations near the InGaAs/InGaP interface, leading to a nearly defect-free region at the top of the fin. A growth mechanism is proposed to account for the correlation between strain accommodation, composition grading, and defects generation.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2016
    detail.hit.zdb_id: 2438749-6
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  • 7
    Online Resource
    Online Resource
    Elsevier BV ; 2009
    In:  Acta Materialia Vol. 57, No. 11 ( 2009-06), p. 3182-3191
    In: Acta Materialia, Elsevier BV, Vol. 57, No. 11 ( 2009-06), p. 3182-3191
    Type of Medium: Online Resource
    ISSN: 1359-6454
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2009
    detail.hit.zdb_id: 1293999-7
    detail.hit.zdb_id: 2014621-8
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  • 8
    In: Biomaterials, Elsevier BV, Vol. 102 ( 2016-09), p. 249-258
    Type of Medium: Online Resource
    ISSN: 0142-9612
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
    detail.hit.zdb_id: 2004010-6
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    Museum and Institute of Zoology at the Polish Academy of Sciences ; 2019
    In:  Polish Journal of Ecology Vol. 67, No. 3 ( 2019-12-9), p. 175-
    In: Polish Journal of Ecology, Museum and Institute of Zoology at the Polish Academy of Sciences, Vol. 67, No. 3 ( 2019-12-9), p. 175-
    Type of Medium: Online Resource
    ISSN: 1505-2249
    Language: Unknown
    Publisher: Museum and Institute of Zoology at the Polish Academy of Sciences
    Publication Date: 2019
    detail.hit.zdb_id: 2322813-1
    detail.hit.zdb_id: 1439083-8
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Frontiers Media SA ; 2022
    In:  Frontiers in Genetics Vol. 13 ( 2022-8-11)
    In: Frontiers in Genetics, Frontiers Media SA, Vol. 13 ( 2022-8-11)
    Abstract: Background: Diffuse large B-cell lymphoma (DLBCL), which is considered to be the most common subtype of lymphoma, is an aggressive tumor. Necroptosis, a novel type of programmed cell death, plays a bidirectional role in tumors and participates in the tumor microenvironment to influence tumor development. Targeting necroptosis is an intriguing direction, whereas its role in DLBCL needs to be further discussed. Methods: We obtained 17 DLBCL-associated necroptosis-related genes by univariate cox regression screening. We clustered in GSE31312 depending on their expressions of these 17 genes and analyzed the differences in clinical characteristics between different clusters. To investigate the differences in prognosis across distinct clusters, the Kaplan-Meier method was utilized. The variations in the tumor immune microenvironment (TME) between distinct necroptosis-related clusters were investigated via “ESTIMATE”, “Cibersort” and single-sample geneset enrichment analysis (ssGSEA). Finally, we constructed a 6-gene prognostic model by lasso-cox regression and subsequently integrated clinical features to construct a prognostic nomogram. Results: Our analysis indicated stable but distinct mechanism of action of necroptosis in DLBCL. Based on necroptosis-related genes and cluster-associated genes, we identified three groups of patients with significant differences in prognosis, TME, and chemotherapy drug sensitivity. Analysis of immune infiltration in the TME showed that cluster 1, which displayed the best prognosis, was significantly infiltrated by natural killer T cells, dendritic cells, CD8 + T cells, and M1 macrophages. Cluster 3 presented M2 macrophage infiltration and the worst prognosis. Importantly, the prognostic model successfully differentiated high-risk from low-risk patients, and could forecast the survival of DLBCL patients. And the constructed nomogram demonstrated a remarkable capacity to forecast the survival time of DLBCL patients after incorporating predictive clinical characteristics. Conclusion: The different patterns of necroptosis explain its role in regulating the immune microenvironment of DLBCL and the response to R-CHOP treatment. Systematic assessment of necroptosis patterns in patients with DLBCL will help us understand the characteristics of tumor microenvironment cell infiltration and aid in the development of tailored therapy regimens.
    Type of Medium: Online Resource
    ISSN: 1664-8021
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2022
    detail.hit.zdb_id: 2606823-0
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