SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Chen Zhihui) "

Sökning: WFRF:(Chen Zhihui)

  • Resultat 1-10 av 15
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Du, Mulong, et al. (författare)
  • Cyp2a6 activity and cigarette consumption interact in smoking-related lung cancer susceptibility
  • 2024
  • Ingår i: Cancer Research. - : American Association For Cancer Research (AACR). - 0008-5472 .- 1538-7445. ; 84:4, s. 616-625
  • Tidskriftsartikel (refereegranskat)abstract
    • Cigarette smoke, containing both nicotine and carcinogens, causes lung cancer. However, not all smokers develop lung cancer, highlighting the importance of the interaction between host susceptibility and environmental exposure in tumorigenesis. Here, we aimed to delineate the interaction between metabolizing ability of tobacco carcinogens and smoking intensity in mediating genetic susceptibility to smoking-related lung tumorigenesis. Single-variant and gene-based associations of 43 tobacco carcinogen–metabolizing genes with lung cancer were analyzed using summary statistics and individual-level genetic data, followed by causal inference of Mendelian randomization, mediation analysis, and structural equation modeling. Cigarette smoke–exposed cell models were used to detect gene expression patterns in relation to specific alleles. Data from the International Lung Cancer Consortium (29,266 cases and 56,450 controls) and UK Biobank (2,155 cases and 376,329 controls) indicated that the genetic variant rs56113850 C>T located in intron 4 of CYP2A6 was significantly associated with decreased lung cancer risk among smokers (OR = 0.88, 95% confidence interval = 0.85–0.91, P = 2.18 X 10-16), which might interact (Pinteraction = 0.028) with and partially be mediated (ORindirect = 0.987) by smoking status. Smoking intensity accounted for 82.3% of the effect of CYP2A6 activity on lung cancer risk but entirely mediated the genetic effect of rs56113850. Mechanistically, the rs56113850 T allele rescued the downregulation of CYP2A6 caused by cigarette smoke exposure, potentially through preferential recruitment of transcription factor helicase-like transcription factor. Together, this study provides additional insights into the interplay between host susceptibility and carcinogen exposure in smoking-related lung tumorigenesis.
  •  
2.
  • Kristan, Matej, et al. (författare)
  • The Sixth Visual Object Tracking VOT2018 Challenge Results
  • 2019
  • Ingår i: Computer Vision – ECCV 2018 Workshops. - Cham : Springer Publishing Company. - 9783030110086 - 9783030110093 ; , s. 3-53
  • Konferensbidrag (refereegranskat)abstract
    • The Visual Object Tracking challenge VOT2018 is the sixth annual tracker benchmarking activity organized by the VOT initiative. Results of over eighty 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 and a “real-time” experiment simulating a situation where a tracker processes images as if provided by a continuously running sensor. A long-term tracking subchallenge has been introduced to the set of standard VOT sub-challenges. The new subchallenge focuses on long-term tracking properties, namely coping with target disappearance and reappearance. A new dataset has been compiled and a performance evaluation methodology that focuses on long-term tracking capabilities has been adopted. The VOT toolkit has been updated to support both standard short-term and the new long-term tracking subchallenges. 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 (http://votchallenge.net).
  •  
3.
  • Chen, Hang, et al. (författare)
  • GRP75 upregulates clathrin-independent endocytosis through actin cytoskeleton reorganization mediated by the concurrent activation of Cdc42 and RhoA
  • 2016
  • Ingår i: Experimental Cell Research. - : Elsevier BV. - 0014-4827. ; 343:2, s. 223-236
  • Tidskriftsartikel (refereegranskat)abstract
    • Therapeutic macromolecules are internalized into the cell by either clathrin-mediated endocytosis (CME) or clathrin-independent endocytosis (CIE). Although some chaperone proteins play an essential role in CME (e.g. Hsc70 in clathrin uncoating), relatively few of these proteins are functionally involved in CIE. We previously revealed a role for the mitochondrial chaperone protein GRP75 in heparan sulfate proteoglycan (HSPG)-mediated, membrane raft-associated macromolecule endocytosis. However, the mechanism underlying this process remains unclear. In this study, using a mitochondrial signal peptide-directed protein trafficking expression strategy, we demonstrate that wild-type GRP75 expression enhanced the uptakes of HSPG and CIE marker cholera toxin B subunit but impaired the uptake of CME marker transferrin. The endocytosis regulation function of GRP75 is largely mediated by its subcellular location in mitochondria and is essentially determined by its ATPase domain. Interestingly, the mitochondrial expression of GRP75 or its ATPase domain significantly stimulates increases in both RhoA and Cdc42 activation, remarkably induces stress fibers and enhances filopodia formation, which collectively results in the promotion of CIE, but the inhibition of CME. Furthermore, silencing of Cdc42 or RhoA impaired the ability of GRP75 overexpression to increase CIE. Therefore, these results suggest that endocytosis vesicle enrichment of GRP75 by mitochondria trafficking upregulates CIE through an actin cytoskeleton reorganization mechanism mediated by the concurrent activation of Cdc42 and RhoA. This finding provides novel insight into organelle-derived chaperone signaling and the regulation of different endocytosis pathways in cells.
  •  
4.
  • Chen, W., et al. (författare)
  • Revealing the Position Effect of an Alkylthio Side Chain in Phenyl-Substituted Benzodithiophene-Based Donor Polymers on the Photovoltaic Performance of Non-Fullerene Organic Solar Cells
  • 2019
  • Ingår i: ACS Applied Materials & Interfaces. - : American Chemical Society (ACS). - 1944-8252 .- 1944-8244. ; 11:36, s. 33173-33178
  • Tidskriftsartikel (refereegranskat)abstract
    • In this work, position effects of an alkylthio side chain were investigated by designing and synthesizing two copolymers based on a phenyl-substituted benzo[1,2-b:4,5-b′]dithiophene (BDTP) and difluorobenzotriazole (FTAZ). The polymer based on the meta-position-alkylthiolated BDTP, named m-PBDTPS-FTAZ, showed a relatively broader bandgap (2.00 vs 1.96 eV) and lower highest occupied molecular orbital (HOMO) energy level (-5.40 vs-5.32 eV) than its para-positioned structural isomeric analogue polymer (named p-PBDTPS-FTAZ), that is, m- A nd p-PBDTPS-FTAZ with the side chain structured as ethylhexyl-in the phenyl unit and hexyldecyl-in the FTAZ moiety. When blended with ITIC, m-PBDTPS-FTAZ showed a comparable crystallinity but more uniform morphology compared to that of p-PBDTPS-FTAZ. A high power conversion efficiency of 13.16% was achieved for m-PBDTPS-FTAZ:ITIC devices with a high open circuit voltage (VOC) of 0.95 V, which is higher than that of p-PBDTPS-FTAZ:ITIC devices (10.86%) with a VOC of 0.89 V. Therefore, m-BDTPS could be an effective donor unit to construct high-efficiency polymers due to its effectively decreased HOMO energy level of polymers while still maintaining good molecular stacking.
  •  
5.
  • Chen, Zhihui, et al. (författare)
  • Exciton Polariton Contribution to the Stokes Shift in Colloidal Quantum Dots
  • 2011
  • Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 115:13, s. 5286-5293
  • Tidskriftsartikel (refereegranskat)abstract
    • We study the exciton polariton contribution to the Stokes shift in colloidal quantum dots (QDs). By detailed quantum mechanical description of light-matter interaction and temporal analysis of incident electromagnetic field across the QD using the finite-difference time-domain method, we have shown that the optical excitation of an exciton in the QD and its coupling with the excitation radiation (i.e., exciton polariton) induce strong variations in the dielectric constant of the QD which contribute significantly to the Stokes shift and cause modifications 50 in the absorption spectrum that agrees well with experiments.
  •  
6.
  •  
7.
  • Chen, Zhihui, 1984- (författare)
  • Light manipulation in micro and nano photonic materials and structures
  • 2012
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Light manipulation is an important method to enhance the light-matter interactions in micro and nano photonic materials and structures by generating usefulelectric field components and increasing time and pathways of light propagationthrough the micro and nano materials and structures. For example, quantum wellinfrared photodetector (QWIP) cannot absorb normal incident radiation so thatthe generation of an electric field component which is parallel to the original incident direction is a necessity for the function of QWIP. Furthermore, the increaseof time and pathways of light propagation in the light-absorbing quantum wellregion will increase the chance of absorbing the photons.The thesis presents the theoretical studies of light manipulation and light-matter interaction in micro and nano photonic materials and structures, aiming atimproving the performance of optical communication devices, photonic integrateddevices and photovoltaic devices.To design efficient micro and nano photonic devices, it is essential to knowthe time evolution of the electromagnetic (EM) field. Two-dimensional and three-dimensional finite-difference time-domain (FDTD) methods have been adopted inthe thesis to numerically solve the Maxwell equations in micro and nano photonicmaterials and structures.Light manipulation in micro and nano material and structures studied in thisthesis includes: (1) light transport in the photonic crystal (PhC) waveguide, (2)light diffraction by the micro-scale dielectric PhC and metallic PhC structures(gratings); and (3) exciton-polaritons of semiconductor quantum dots, (4) surfaceplasmon polaritons at semiconductor-metallic material interface for subwavelengthlight control. All these aspects are found to be useful in optical devices of multiplebeam splitter, quantum well/dot infrared photodetectors, and solar cells.
  •  
8.
  • Chen, Zhihui, et al. (författare)
  • Multiple beam splitting to free space from a V groove in a photonic crystal waveguide
  • 2011
  • Ingår i: Applied physics. B, Lasers and optics (Print). - : Springer Science and Business Media LLC. - 0946-2171 .- 1432-0649. ; 102:4, s. 857-861
  • Tidskriftsartikel (refereegranskat)abstract
    • We present multiple-beam splitting to free space from a V groove in a two-dimensional photonic crystal waveguide (PCW) with a few additional dielectric rods at the exit of the PCW. Numerical study shows that 'one-beam-in to two-beams-out' (one-to-two, also denoted as Y-shaped), one-to-three, and one-to-five beam splittings can be easily realized over a wide bandwidth, and the split beams have remarkable properties such as symmetric energy distributions and high directional transmissions. Off-axis directional emission can also be achieved by simple displacements of the additional rods at the exit of the PCW.
  •  
9.
  • Chen, Zhihui, et al. (författare)
  • Time-resolved photocurrents in quantum well/dot infrared photodetectors with different optical coupling structures
  • 2012
  • Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 100:4, s. 043502-
  • Tidskriftsartikel (refereegranskat)abstract
    • Temporal developments of photocurrents excited by an infrared radiation pulse in quantum well/dot infrared photodetectors with different optical coupling structures have been theoretically studied. It is shown that the light diffraction in a conventional reflective grating structure is a near-field effect containing severe crosstalk from neighboring pixels. A concave reflector not only eliminates the crosstalk but also strongly diffracts and focuses the incident electric field into deep active layers, which significantly increases the photocurrents in the photodetectors.
  •  
10.
  • Gao, Zhihui, et al. (författare)
  • Mitochondria chaperone GRP75 moonlighting as a cell cycle controller to derail endocytosis provides an opportunity for nanomicrosphere intracellular delivery
  • 2017
  • Ingår i: Oncotarget. - : Impact Journals, LLC. - 1949-2553. ; 8:35, s. 58536-58552
  • Tidskriftsartikel (refereegranskat)abstract
    • Understanding how cancer cells regulate endocytosis during the cell cycle could lead us to capitalize this event pharmacologically. Although certain endocytosis pathways are attenuated during mitosis, the endocytosis shift and regulation during the cell cycle have not been well clarified. The conventional concept of glucose-regulated proteins (GRPs) as protein folding chaperones was updated by discoveries that translocated GRPs assume moonlighting functions that modify the immune response, regulate viral release, and control intracellular trafficking. In this study, GRP75, a mitochondria matrix chaperone, was discovered to be highly expressed in mitotic cancer cells. Using synchronized cell models and the GRP75 gene knockdown and ectopic overexpression strategy, we showed that: (1) clathrin-mediated endocytosis (CME) was inhibited whereas clathrinindependent endocytosis (CIE) was unchanged or even up-regulated in the cell cycle M-phase; (2) GRP75 inhibited CME but promoted CIE in the M-phase, which is largely due to its high expression in cancer cell mitochondria; (3) GRP75 targeting by its small molecular inhibitor MKT-077 enhanced cell cycle G1 phase-privileged CME, which provides an opportunity for intracellular delivery of nanomicrospheres sized from 40 nm to 100 nm. Together, our results revealed that GRP75 moonlights as a cell cycle controller and endocytosis regulator in cancer cells, and thus has potential as a novel interference target for nanoparticle drugs delivery into dormant cancer cells.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 15
Typ av publikation
tidskriftsartikel (12)
konferensbidrag (2)
doktorsavhandling (1)
Typ av innehåll
refereegranskat (14)
övrigt vetenskapligt/konstnärligt (1)
Författare/redaktör
Wang, Qiang (2)
Qiu, Min (2)
Belting, Mattias (2)
Chen, W. (1)
Yang, R. (1)
Wang, Q. (1)
visa fler...
Wang, Dong (1)
Chen, Deliang, 1961 (1)
Albanes, Demetrius (1)
Li, Yan (1)
Grankvist, Kjell (1)
Rennert, Gad (1)
Li, Jing (1)
Johansson, Mattias (1)
Cao, Yang, Associate ... (1)
Bojesen, Stig E. (1)
Cox, Angela (1)
Le Marchand, Loïc (1)
Mishra, Deepak (1)
Wichmann, H. Erich (1)
Brennan, Paul (1)
Johansson, Mikael (1)
Wang, Ergang, 1981 (1)
Li, Xiaoming (1)
Kiemeney, Lambertus ... (1)
He, Jia (1)
van de Weijer, Joost (1)
Amos, Christopher I. (1)
Wei, Qingyi (1)
Yang, Fan (1)
Andersson, J. Y. (1)
He, Sailing (1)
Risch, Angela (1)
Aldrich, Melinda C (1)
Li, Zhen (1)
Li, Bo (1)
Zhang, Yichi (1)
Wang, Huan (1)
Bai, Shuai (1)
Landi, Maria Teresa (1)
van Kuppevelt, Toin ... (1)
Ning, Zhijun (1)
Wu, Yi (1)
Felsberg, Michael, 1 ... (1)
Johnander, Joakim (1)
Caporaso, Neil E. (1)
Bhat, Goutam (1)
Danelljan, Martin, 1 ... (1)
Khan, Fahad Shahbaz, ... (1)
Wu, Xiaohe (1)
visa färre...
Lärosäte
Kungliga Tekniska Högskolan (7)
Lunds universitet (2)
Göteborgs universitet (1)
Umeå universitet (1)
Stockholms universitet (1)
Örebro universitet (1)
visa fler...
Linköpings universitet (1)
Chalmers tekniska högskola (1)
visa färre...
Språk
Engelska (15)
Forskningsämne (UKÄ/SCB)
Naturvetenskap (8)
Medicin och hälsovetenskap (5)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy