1. |
- Kristanl, Matej, et al.
(författare)
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The Seventh Visual Object Tracking VOT2019 Challenge Results
- 2019
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Ingår i: 2019 IEEE/CVF INTERNATIONAL CONFERENCE ON COMPUTER VISION WORKSHOPS (ICCVW). - : IEEE COMPUTER SOC. - 9781728150239 ; , s. 2206-2241
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Konferensbidrag (refereegranskat)abstract
- The Visual Object Tracking challenge VOT2019 is the seventh annual tracker benchmarking activity organized by the VOT initiative. Results of 81 trackers are presented; many are state-of-the-art trackers published at major computer vision conferences or in journals in the recent years. The evaluation included the standard VOT and other popular methodologies for short-term tracking analysis as well as the standard VOT methodology for long-term tracking analysis. The VOT2019 challenge was composed of five challenges focusing on different tracking domains: (i) VOT-ST2019 challenge focused on short-term tracking in RGB, (ii) VOT-RT2019 challenge focused on "real-time" short-term tracking in RGB, (iii) VOT-LT2019 focused on long-term tracking namely coping with target disappearance and reappearance. Two new challenges have been introduced: (iv) VOT-RGBT2019 challenge focused on short-term tracking in RGB and thermal imagery and (v) VOT-RGBD2019 challenge focused on long-term tracking in RGB and depth imagery. The VOT-ST2019, VOT-RT2019 and VOT-LT2019 datasets were refreshed while new datasets were introduced for VOT-RGBT2019 and VOT-RGBD2019. The VOT toolkit has been updated to support both standard short-term, long-term tracking and tracking with multi-channel imagery. Performance of the tested trackers typically by far exceeds standard baselines. The source code for most of the trackers is publicly available from the VOT page. The dataset, the evaluation kit and the results are publicly available at the challenge website(1).
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2. |
- Li, Cong, et al.
(författare)
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Targeted therapy with anlotinib for a leptomeningeal spread recurrent glioblastoma patient
- 2021
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Ingår i: NANOMEDICINE AND NEUROPROTECTION IN BRAIN DISEASES. - : ELSEVIER ACADEMIC PRESS INC. - 9780323901628 ; , s. 407-414
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Bokkapitel (refereegranskat)abstract
- Glioblastoma (GBM) is the most common and the most aggressive primary malignant brain tumor in adults. Although tumor recurrence is inevitable, leptomeningeal spread is relatively rare. We describe a case of leptomeningeal spread recurrent GBM treated with anlotinib in this report. When the recurrent GBM patient had leptomeningeal spread was administered anlotinib 10mg p.o. once every day and added oral temozolomide chemotherapy 100mg/m(2) (days 1-7, days 15-21, 28-day cycle) after 3 months. The patient's overall survival time was more than 5 months and developed oral ulcer and acute cerebral infarction during his oral administration of anlotinib. This patient showed a favorable clinic outcome for treatment of leptomeningeal spread recurrent GBM with anlotinib and didn't show serious side effects.
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3. |
- Li, Luhan, et al.
(författare)
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Tailoring charge reconfiguration in dodecahedral Co2P@carbon nanohybrids by triple-doping engineering for promoted reversible oxygen catalysis
- 2022
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 10:40, s. 21659-21671
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Tidskriftsartikel (refereegranskat)abstract
- Simultaneously tuning the electronic structure of active sites and the microenvironment of the carbon matrix in metal phosphide/carbon nanohybrids is the most effective way to design and develop bi-functional electrocatalysts for electrochemically related energy storage devices. Inspired by this, a robust and advanced N/P co-doped carbon-based dodecahedron catalyst with confined Fe-doped Co2P particles was successfully prepared through a multi-doping engineering strategy. Phytic acid molecules, which were used in the synthesis of the catalyst, not only contribute to the formation of the porous structure, but also act as a phosphorus source to form the corresponding metal phosphide and the P dopant in the carbon matrix. Thanks to the unique composition and structure-dependent merits, the microenvironment of the electrocatalyst was significantly modulated, thus promoting the advantageous local charge rearrangement and smooth mass/charge transfer processes during the oxygen-related electrocatalytic reactions. As a result, the resultant catalyst exhibited significantly enhanced reversible oxygen activity, as evidenced by an ultra-small potential gap of 0.655 V (half-wave potential of 0.895 V for the oxygen reduction reaction; η10 of 320 mV for the oxygen evolution reaction), a remarkable specific capacity of 762 mA h gZn−1, and high voltaic efficiency, exceeding most previous reports. This study provides a new synthetic approach for fabricating highly efficient bi-functional oxygen catalysts and can be handily extended to the synthesis of other heterogeneous electrocatalysts for sustainable energy storage.
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4. |
- Li, Shuijie, et al.
(författare)
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Impaired oxygen-sensitive regulation of mitochondrial biogenesis within the von Hippel–Lindau syndrome
- 2022
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Ingår i: Nature Metabolism. - : Nature Publishing Group. - 2522-5812. ; 4:6, s. 739-758
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Tidskriftsartikel (refereegranskat)abstract
- Mitochondria are the main consumers of oxygen within the cell. How mitochondria sense oxygen levels remains unknown. Here we show an oxygen-sensitive regulation of TFAM, an activator of mitochondrial transcription and replication, whose alteration is linked to tumours arising in the von Hippel–Lindau syndrome. TFAM is hydroxylated by EGLN3 and subsequently bound by the von Hippel–Lindau tumour-suppressor protein, which stabilizes TFAM by preventing mitochondrial proteolysis. Cells lacking wild-type VHL or in which EGLN3 is inactivated have reduced mitochondrial mass. Tumorigenic VHL variants leading to different clinical manifestations fail to bind hydroxylated TFAM. In contrast, cells harbouring the Chuvash polycythaemia VHLR200W mutation, involved in hypoxia-sensing disorders without tumour development, are capable of binding hydroxylated TFAM. Accordingly, VHL-related tumours, such as pheochromocytoma and renal cell carcinoma cells, display low mitochondrial content, suggesting that impaired mitochondrial biogenesis is linked to VHL tumorigenesis. Finally, inhibiting proteolysis by targeting LONP1 increases mitochondrial content in VHL-deficient cells and sensitizes therapy-resistant tumours to sorafenib treatment. Our results offer pharmacological avenues to sensitize therapy-resistant VHL tumours by focusing on the mitochondria.
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5. |
- Zarkada, Georgia, et al.
(författare)
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Chylomicrons Regulate Lacteal Permeability and Intestinal Lipid Absorption
- 2023
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Ingår i: Circulation Research. - : Lippincott Williams & Wilkins. - 0009-7330 .- 1524-4571. ; 133:4, s. 333-349
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Tidskriftsartikel (refereegranskat)abstract
- Background: Lymphatic vessels are responsible for tissue drainage, and their malfunction is associated with chronic diseases. Lymph uptake occurs via specialized open cell-cell junctions between capillary lymphatic endothelial cells (LECs), whereas closed junctions in collecting LECs prevent lymph leakage. LEC junctions are known to dynamically remodel in development and disease, but how lymphatic permeability is regulated remains poorly understood.Methods: We used various genetically engineered mouse models in combination with cellular, biochemical, and molecular biology approaches to elucidate the signaling pathways regulating junction morphology and function in lymphatic capillaries.Results: By studying the permeability of intestinal lacteal capillaries to lipoprotein particles known as chylomicrons, we show that ROCK (Rho-associated kinase)-dependent cytoskeletal contractility is a fundamental mechanism of LEC permeability regulation. We show that chylomicron-derived lipids trigger neonatal lacteal junction opening via ROCK-dependent contraction of junction-anchored stress fibers. LEC-specific ROCK deletion abolished junction opening and plasma lipid uptake. Chylomicrons additionally inhibited VEGF (vascular endothelial growth factor)-A signaling. We show that VEGF-A antagonizes LEC junction opening via VEGFR (VEGF receptor) 2 and VEGFR3-dependent PI3K (phosphatidylinositol 3-kinase)/AKT (protein kinase B) activation of the small GTPase RAC1 (Rac family small GTPase 1), thereby restricting RhoA (Ras homolog family member A)/ROCK-mediated cytoskeleton contraction.Conclusions: Our results reveal that antagonistic inputs into ROCK-dependent cytoskeleton contractions regulate the interconversion of lymphatic junctions in the intestine and in other tissues, providing a tunable mechanism to control the lymphatic barrier.
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6. |
- Arif, Muhammad, et al.
(författare)
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INetModels 2.0: An interactive visualization and database of multi-omics data
- 2021
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Ingår i: Nucleic Acids Research. - : Oxford University Press (OUP). - 0305-1048 .- 1362-4962. ; 49:W1, s. W271-W276
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Tidskriftsartikel (refereegranskat)abstract
- It is essential to reveal the associations between various omics data for a comprehensive understanding of the altered biological process in human wellness and disease. To date, very few studies have focused on collecting and exhibiting multi-omics associations in a single database. Here, we present iNetModels, an interactive database and visualization platform of Multi-Omics Biological Networks (MOBNs). This platform describes the associations between the clinical chemistry, anthropometric parameters, plasma proteomics, plasma metabolomics, as well as metagenomics for oral and gut microbiome obtained from the same individuals. Moreover, iNetModels includes tissue- and cancer-specific Gene Co-expression Networks (GCNs) for exploring the connections between the specific genes. This platform allows the user to interactively explore a single feature's association with other omics data and customize its particular context (e.g. male/female specific). The users can also register their data for sharing and visualization of the MOBNs and GCNs. Moreover, iNetModels allows users who do not have a bioinformatics background to facilitate human wellness and disease research. iNetModels can be accessed freely at https://inetmodels.com without any limitation.
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7. |
- Jiang, Ruijie, et al.
(författare)
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Substantial increase in future fluvial flood risk projected in China’s major urban agglomerations
- 2023
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Ingår i: Communications Earth and Environment. - 2662-4435. ; 4
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Tidskriftsartikel (refereegranskat)abstract
- Urban land will face high fluvial flood risk against the background of climate change and urban expansion. The effect of urban spatial expansion, instead of densification of assets within existing urban cells, on flood risk has rarely been reported. Here, we project the future flood risk of seven urban agglomerations in China, home to over 750 million people. The inundated urban land areas in the future are projected to be 4 to 19 times that at present. Without considering the urban spatial expansion, the inundated urban land areas will be underestimated by 10-50%. Urban land is more likely to be inundated than non-urban land, and the newly-developed urban land will be inundated more easily than the historical urban land. The results demonstrate the urgency of integrating climate change mitigation, reasonable urban land expansion, and increased flood protection levels to minimize the flood risk in urban land.
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8. |
- Li, Wenyu
(författare)
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Exploring inter- and intra-heterogeneity in childhood neuroblastoma and pheochromocytoma
- 2022
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Neuroblastoma is the most common extra-cranial solid tumor of the sympathoadrenal cell lineage, which is a unique pediatric malignancy with remarkable inter- and intra-tumoral heterogeneity. In infants, neuroblastoma can regress spontaneously without treatment, while in older patients, neuroblastoma can develop with lethal progression with less than a 50% survival rate. Age at diagnosis is a clinically relevant prognosis factor. Chemoresistance in neuroblastoma patients has been associated with tumor cell plasticity and intratumoral heterogeneity. However, the causes of tumor cell plasticity and intratumoral heterogeneity are not well understood. In Paper I, we aim to investigate the in vivo function of KIF1Bβ in the sympathoadrenal system. KIF1Bβ locates on chromosome 1p36. Loss of heterozygosity at 1p36 strongly correlates with a poor prognosis of neuroblastoma. KIF1Bβ has been suggested to be a 1p36 tumor suppressor gene and demonstrated to be required for neuroblast developmental apoptosis. We showed that the loss of KIF1Bβ impairs neuroblast differentiation during development and causes misexpression of genes required for sympathoadrenal differentiation. We demonstrated that KIF1Bβ mediates neuroblast differentiation by transporting the NGF receptor TRKA. Transcriptomic analysis revealed that KIF1Bβ deficient sympathetic neuroblasts is similar to the profile in non-MYCN amplified high-risk neuroblastoma, independent of the loss of KIF1Bβ neighboring genes on 1p36. In Paper II, we found that loss of NF1 alone or in combination NF1 with KIF1Bβ in mouse sympathoadrenal lineage leads to neuroblastoma, pheochromocytoma, and composite tumors. In addition, mice with NF1 and KIF1Bβ loss have earlier tumor death onset and lower survival probability compared to NF1 loss alone. The single-cell sequencing of tumors and embryonic(E17) adrenal medulla showed a remarkable heterogeneity of chromaffin cells and neuroblasts. Importantly, we observed abundant neuroblasts born in the adrenal medulla in the E17 embryo. Furthermore, computational analysis reveals a cell state transition from chromaffin cells to neuroblasts in embryonic and pre-malignant stages. The chromaffin neuroblasts transition has also been observed in a three-segment structure in which chromaffin cells break through the cortex, suggesting that chromaffin cells acquire neuroblast signature and continue to form neuroblastoma, pheochromocytoma and composite tumors. In Paper III, we explored the inter- and intra-tumoral heterogeneity in human neuroblastoma and why age at diagnosis is one of the important prognostic factors. We analyzed the singlenuclei transcriptomes of human healthy fetal and postnatal adrenal glands and primary neuroblastomas from different stages and risk groups. We found two disease entities with varying signatures of cells in low and high-risk neuroblastoma. Notably, the transcriptome of high-risk neuroblastoma resembles a TRKB+ cholinergic progenitor cell population characterized specifically in the human postnatal adrenal glands. Thus, our study reveals two cellular identities reflecting the clinical heterogeneity of neuroblastoma tumors.
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9. |
- Lin, Qing, et al.
(författare)
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Exosome-like nanoplatform modified with targeting ligand improves anti-cancer and anti-inflammation effects of imperialine
- 2019
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Ingår i: Journal of Controlled Release. - : ELSEVIER. - 0168-3659 .- 1873-4995. ; 311, s. 104-116
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Tidskriftsartikel (refereegranskat)abstract
- Currently, most anti-cancer therapies are still haunted by serious and deleterious adverse effects. Here, we report a highly biocompatible tumor cell-targeting delivery systems utilizing exosome-like vesicles (ELVs) that delivers a low-toxicity anti-cancer agent imperialine against non-small cell lung cancer (NSCLC). First, we introduced a novel micelle-aided method to efficiently load imperialine into intact ELVs. Then, integrin alpha 3 beta 1-binding octapeptide cNGQGEQc was modified onto ELV platform for tumor targeting as integrin alpha 3 beta 1 is overexpressed on NSCLC cells. This system not only significantly improved imperialine tumor accumulation and retention, but also had extremely low systemic toxicity both in vitro and in vivo. Our discoveries offer new ways to utilize ELV more efficiently for both drug loading and targeting. The solid pharmacokinetics improvement and extraordinary safety of this system also highlight possibilities of alternative long course cancer therapies using similar strategies.
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10. |
- Maslyk, Marcel, et al.
(författare)
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Understanding the Stability and Recrystallization Behavior of Amorphous Zinc Phosphate
- 2021
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 125:4, s. 2636-2647
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Tidskriftsartikel (refereegranskat)abstract
- Zinc phosphate, an important pigment in phosphate conversion coatings, forms protective films on rubbing surfaces. We have simulated the underlying reactions under shear by ball-milling zinc phosphate and monitored the reaction of hopeite (Zn3(PO4)2·4H2O) and the retarded recrystallization of the amorphous reaction product by powder X-ray diffraction (PXRD) and quantitative infrared (IR) spectroscopy. Abrasion of stainless steel was simulated by addition of pure 57Fe. The results provide insight into the chemistry of phosphate conversion coatings or during battery cycling of metal phosphates and give theoretical guidance for the preparation of amorphous phosphates. Thermal analysis revealed that the release of structural water is a key step during the reaction of hopeite under shear to ball-milled amorphous zinc phosphate. The back-reaction and associated recrystallization kinetics of amorphous zinc phosphate show a classical Langmuir behavior. Fe impurities inhibit the recrystallization of ball-milled amorphous zinc phosphate strongly. 57Fe Mössbauer spectroscopy and PXRD revealed that Fe is oxidized to Fe2+ and Fe3+ during ball-milling and incorporated locally at the tetrahedral and octahedral sites of the structure. Ball-milled amorphous zinc phosphate is metastable as γ-Zn3–xFex(PO4)2. EPR studies showed the incorporation of Fe3+ to be coupled with the formation of Zn2+ vacancies. The Fe3+ defect sites bind water because of their higher Pearson hardness (compared to Fe2+ and Zn2+), thereby reducing water mobility and inhibiting further reactions like the recrystallization to hopeite. Our findings reveal the amorphization mechanism of Zn3(PO4)2·4H2O in stainless steel ball mills at the atomic scale and highlight how the reactivity of amorphous products is affected by impurities associated with the processing method.
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