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- 저자 : Huang Xiao-Fang (검색결과 33 건)
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5,10-Methylenetetrahydrofolate Reductase Polymorphisms and Colon Cancer Risk: a Meta-analysis
Fang, Xin-Yu,Xu, Wang-Dong,Huang, Qian,Yang, Xiao-Ke,Liu, Yan-Yan,Leng, Rui-Xue,Pan, Hai-Feng,Ye, Dong-Qing Asian Pacific Journal of Cancer Prevention 2014 Asian Pacific journal of cancer prevention Vol.15 No.19
Previous studies investigating the association between 5,10-methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and colon cancer risk have generated conflicting results. The aim of our meta-analysis was to clarify the precise association. A systematic literature search was conducted to identify all relevant studies. Pooled odds ratio (ORs) with 95% confidence interval (CI) were used to estimate the strength of the association. In this meta-analysis, a total of 13 articles, involving 5,386 cases and 8,017 controls met the inclusion criteria. Overall, a significant association was found between colon cancer risk and the MTHFR C667 polymorphism (TT vs CC+CT: OR=0.79; 95%CI=0.65-0.96; p=0.017). Stratification by ethnicity revealed that MTHFRC667 was associated with colon cancer risk in the non-Asian group (TT vs CC+CT:OR=0.77, 95%CI=0.68-0.89, p=0.000; TT vs CC: OR=0.84, 95%CI=0.73-0.97, p=0.016). Stratification by source of control indicated that MTHFR C667 also correlated with colon cancer risk in the population-based subgroup (TT vs CC: OR=0.85, 95%CI=0.74-0.97, p=0.017; TT vs CC+CT: OR=0.78, 95%CI=0.68-0.89, p=0.000) and hospital-based subgroup (TT vs CC+CT: OR=0.65, 95%CI=0.49-0.86, p=0.003). However, risk was significantly increased for MTHFR A1298C polymorphisms and colon cancer risk in hospital-based studies (C vs A: OR=1.52, 95%CI=1.26-1.83, p=0.000; CC+AC vs AA: OR=1.93, 95%CI=1.47-2.49, p=0.000) but reduced in population-based studies (CC vs AA: OR=0.83, 95%CI=0.70-0.99, p=0.042). In conclusion, the results of our meta-analysis suggest that the MTHFR C667 polymorphism is associated with reduced colon cancer risk, especially for non-Asian populations.
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Knockdown of Chloride Channel-3 Inhibits Breast Cancer Growth In Vitro and In Vivo
Fang-Min Zhou,Yun-Ying Huang,Tian Tian,Xiao Yan Liu,Yong-Bo Tang 한국유방암학회 2018 Journal of breast cancer Vol.21 No.2
Purpose: Chloride channel-3 (ClC-3) is a member of the chloride channel family and plays a critical role in a variety of cellular activities. The aim of the present study is to explore the molecular mechanisms underlying the antitumor effect of silencing ClC-3 in breast cancer. Methods: Human breast cancer cell lines MDAMB- 231 and MCF-7 were used in the experiments. Messenger RNA and protein expression were examined by quantitative realtime polymerase chain reaction and western blot analysis. Cell proliferation was measured by the bromodeoxyuridine method, and the cell cycle was evaluated using fluorescence-activated cell sorting. Protein interaction in cells was analyzed by co-immunoprecipitation. Tumor tissues were stained with hematoxylin- eosin and tumor burden was measured using the Metamorph software. Results: Breast cancer tissues collected from patients showed an increase in ClC-3 expression. Knockdown of ClC-3 inhibited the secretion of insulin-like growth factor (IGF)-1, cell proliferation, and G1/S transition in breast cancer cells. In the mouse xenograft model of human breast carcinoma, tumor growth was significantly slower in animals injected with ClC- 3-deficient cells compared with the growth of normal human breast cancer cells. In addition, silencing of ClC-3 attenuated the expression of proliferating cell nuclear antigen, Ki-67, cyclin D1, and cyclin E, as well as the activation of extracellular signalregulated protein kinases (ERK) 1/2, both in vitro and in vivo. Conclusion: Together, our data suggest that upregulation of ClC- 3 by IGF-1 contributes to cell proliferation and tumor growth in breast cancer, and ClC-3 deficiency suppresses cell proliferation and tumor growth via the IGF/IGF receptor/ERK pathway.
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Fang Zheng,Qing Tang,Xiao-hua Zheng,JingJing Wu,HaiDing Huang,Haibo Zhang,Swei Sunny Hann 생화학분자생물학회 2018 Experimental and molecular medicine Vol.50 No.-
β-Elemene, an active component of natural plants, has been shown to exhibit anticancer properties. However, the detailed mechanism underlying these effects has yet to be determined. In this study, we show that β-elemene inhibits the growth of lung cancer cells. Mechanistically, we found that β-elemene decreased the phosphorylation of signal transducer and activator of transcription 3 (Stat3) and miRNA155-5p mRNA but induced the protein expression of human forkhead box class O (FOXO)3a; the latter two were abrogated in cells with overexpressed Stat3. Notably, miRNA155-5p mimics reduced FOXO3a luciferase reporter activity in the 3-UTR region and protein expression, whereas overexpressed FOXO3a countered the reduction of the miRNA155-5p levels by β-elemene. Moreover, β-elemene increased the mRNA and protein expression levels as well as promoter activity of insulin-like growth factor-binding protein 1 (IGFBP1); this finding was not observed in cells with a silenced FOXO3a gene and miRNA155-5p mimics. Finally, silencing of IGFBP1 blocked β-elemene-inhibited cell growth. Similar findings were observed in vivo. In summary, our results indicate that β-elemene increases IGFBP1 gene expression via inactivation of Stat3 followed by a reciprocal interaction between miRNA155-5p and FOXO3a. This effect leads to inhibition of human lung cancer cell growth. These findings reveal a novel molecular mechanism underlying the inhibitory effects of β-elemene on lung cancer cells.
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Optical Properties of Tm-Er Codoped Aluminate Glasses
Zhisong Xiao,Lu Yan,Bo Zhou,Fang Zhu,Anping Huang,Jinliang Wang,Yongchang Zhu 한국물리학회 2008 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.52 No.-
Transparent CaO-Al₂O₃-B₂O₃ glasses codoped with Tm³+ and Er³+ were prepared by melt quenching and subsequent heating. Optical absorption spectra revealed an ultraviolet to visible absorption band corresponding to a relative electronic transition of Tm3+ and Er³+. For Tm-only doped glasses, the 791-nm absorption line is prominent and also has comparable strength in Tm-Er codoped glasses. Both 405-nm and 791-nm wavelengths have been used as excitation sources to comparatively study the photoluminescence characteristics of Tm3+ and Er3+. Only Er3+ emission at 1528 nm has been observed under a pumping wavelength of 405 nm. However, both Tm3+ and Er³+ emission can be found with an excitation wavelength of 791 nm. It implies that 791 nm should be very effective for pumping Tm-Er codoped aluminate glass for application in broadband optical waveguide amplifiers. Transparent CaO-Al₂O₃-B₂O₃ glasses codoped with Tm³+ and Er³+ were prepared by melt quenching and subsequent heating. Optical absorption spectra revealed an ultraviolet to visible absorption band corresponding to a relative electronic transition of Tm3+ and Er³+. For Tm-only doped glasses, the 791-nm absorption line is prominent and also has comparable strength in Tm-Er codoped glasses. Both 405-nm and 791-nm wavelengths have been used as excitation sources to comparatively study the photoluminescence characteristics of Tm3+ and Er3+. Only Er3+ emission at 1528 nm has been observed under a pumping wavelength of 405 nm. However, both Tm3+ and Er³+ emission can be found with an excitation wavelength of 791 nm. It implies that 791 nm should be very effective for pumping Tm-Er codoped aluminate glass for application in broadband optical waveguide amplifiers.
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( Yan Fang ),( Xiao Jun Huang ),( Peng Cheng Chen ),( Zhi Kang Xu ) 생화학분자생물학회(구 한국생화학분자생물학회) 2011 BMB Reports Vol.44 No.2
Enzymatic catalysis has been pursued extensively in a wide range of important chemical processes for their unparalleled selectivity and mild reaction conditions. However, enzymes are usually costly and easy to inactivate in their free forms. Immobilization is the key to optimizing the in-service performance of an enzyme in industrial processes, particularly in the field of non-aqueous phase catalysis. Since the immobilization process for enzymes will inevitably result in some loss of activity, improving the activity retention of the immobilized enzyme is critical. To some extent, the performance of an immobilized enzyme is mainly governed by the supports used for immobilization, thus it is important to fully understand the properties of supporting materials and immobilization processes. In recent years, there has been growing concern in using polymeric materials as supports for their good mechanical and easily adjustable properties. Furthermore, a great many work has been done in order to improve the activity retention and stabilities of immobilized enzymes. Some introduce a spacer arm onto the support surface to improve the enzyme mobility. The support surface is also modified towards biocompatibility to reduce non-biospecific interactions between the enzyme and support. Besides, natural materials can be used directly as supporting materials owning to their inert and biocompatible properties. This review is focused on recent advances in using polymeric materials as hosts for lipase immobilization by two different methods, surface attachment and encapsulation. Polymeric materials of different forms, such as particles, membranes and nanofibers, are discussed in detail. The prospective applications of immobilized enzymes, especially the enzyme-immobilized membrane bioreactors (EMBR) are also discussed. [BMB reports 2011; 44(2): 87-95]
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Youmei Xiao,Zhanxue Xu,Yuan Cheng,Rufan Huang,Yuan Xie,Hsiang‑i Tsai,Hualian Zha,Lifang Xi,Kai Wang,Xiaoli Cheng,Yanfeng Gao,Changhua Zhang,Fang Cheng,Hongbo Chen 한국생체재료학회 2023 생체재료학회지 Vol.27 No.00
Background Ferroptosis, iron-dependent cell death, is an established mechanism for cancer suppression, particularly in hepatocellular carcinoma (HCC). Sorafenib (SOR), a frontline drug for the treatment of HCC, induces ferroptosis by inhibiting the Solute Carrier family 7 member 11 (SLC7A11), with inadequate ferroptosis notably contributing to SOR resistance in tumor cells. Methods To further verify the biological targets associated with ferroptosis in HCC, an analysis of the Cancer Genome Atlas (TCGA) database was performed to find a significant co-upregulation of SLC7A11 and transferrin receptor (TFRC), Herein, cell membrane-derived transferrin nanovesicles (TF NVs) coupled with Fe3+ and encapsulated SOR (SOR@TF-Fe3+ NVs) were established to synergistically promote ferroptosis, which promoted the iron transport metabolism by TFRC/TF-Fe3+ and enhanced SOR efficacy by inhibiting the SLC7A11. Results In vivo and in vitro experiments revealed that SOR@TF-Fe3+ NVs predominantly accumulate in the liver, and specifically targeted HCC cells overexpressing TFRC. Various tests demonstrated SOR@TF-Fe3+ NVs accelerated Fe3+ absorption and transformation in HCC cells. Importantly, SOR@TF-Fe3+ NVs were more effective in promoting the accumulation of lipid peroxides (LPO), inhibiting tumor proliferation, and prolonging survival rates in HCC mouse model than SOR and TF- Fe3+ NVs alone. Conclusions The present work provides a promising therapeutic strategy for the targeted treatment of HCC.
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Visible Luminescence of Tm3+, Er3+ and Yb3+ in Calcium-Aluminoborate Glasses
Zhisong Xiao,Lu Yan,Fang Zhu,Anping Huang 한국물리학회 2009 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.55 No.6
Tm, Er, and Yb codoped calcium-aluminoborate glasses were prepared. Intense visible luminescence was observed under excitation at a 325-nm wavelength. It was demonstrated that violet and blue luminescences (392, 454 and 478 nm) were mainly contributed by Tm3+, and green (514, 528 and 559 nm) and red (652 nm) luminescences were mainly contributed by Er3+. Energy transfer processes among Tm3+, Er3+, and Yb3+ were evidenced, in which various colors of the luminescence could be easily tuned by adjusting the concentration and the kind of the rare earth ions in glasses. Tm, Er, and Yb codoped calcium-aluminoborate glasses were prepared. Intense visible luminescence was observed under excitation at a 325-nm wavelength. It was demonstrated that violet and blue luminescences (392, 454 and 478 nm) were mainly contributed by Tm3+, and green (514, 528 and 559 nm) and red (652 nm) luminescences were mainly contributed by Er3+. Energy transfer processes among Tm3+, Er3+, and Yb3+ were evidenced, in which various colors of the luminescence could be easily tuned by adjusting the concentration and the kind of the rare earth ions in glasses.
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Wang, Xiao-Xi,Wu, Zheng,Huang, Hui-Fang,Han, Chao,Zou, Wei,Liu, Jing Asian Pacific Journal of Cancer Prevention 2013 Asian Pacific journal of cancer prevention Vol.14 No.4
Background: To explore the role of caveolin-1(CAV-1) gene silencing on MAPK activation in lipopolysaccharide (LPS)-challenged human mammary epithelial cells. Methods: We established a MCF-10ACE of CAV-1 gene silencing from human mammary epithelial cell line MCF-10A by RNAi technology. DNA Microarray were used to detect the expression of inflammation-associated genes in MCF10ACE. Western blotting was used to examine the activation of MAPK in lipopolysaccharide(LPS)-challenged MCF-10A and MCF-10ACE. Moreover, immunofluorescence and Western bloting were performed to detect the co-localization of CAV-1 and toll-like receptor 4 (TLR4) in human mammary epithelial cells. Results: MCF-10ACE exhibited significant increases in inflammation-associated gene expression, especially IL-6 (~7-fold) and IL6R (~17-fold). In addition, LPS-induced p38 MAPK and JNK MAPK activation was significantly increased in MCF-10ACE. Furthermore, CAV-1 co-localized with TLR4 and appeared a negative correlation trend. Conclusion: CAV-1 gene silencing promotes MAPK activation via TLR4 signaling in human mammary epithelial cells response to LPS.
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Li Yue,Xiao Xiao-Bing,He Xiao-Meng,Huang Bo-Yang,Fang Yang,He Xin-Yi 대한전기학회 2024 Journal of Electrical Engineering & Technology Vol.19 No.2
This paper describes a technique for improving distribution network dispatch by using the four-quadrant power output of distributed energy storage systems to address voltage deviation and grid loss problems resulting from the large integration of distributed generation into the distribution network. The approach creates an optimization dispatch model for an active distribution network. The objective function aims to minimize power purchase costs, network loss costs, and voltage deviation penalties. In addition, the method employs an interval robust optimization technique to handle uncertainties related to solar turbine output and load demand. To solve the optimal power fow problem for AC in the distribution network, this paper implements the second-order cone relaxation technique to convert it into a solvable second-order cone programming problem. Moreover, the Big-M method is used to handle the nonlinear terms in the objective function. Finally, simulation experiments are conducted on the IEEE33 node system to verify the efectiveness and superiority of the proposed method. The simulation results indicate that the system's operating cost can be signifcantly reduced. Additionally, it has a positive impact on reducing voltage deviation and system loss, ultimately improving the operation of the distribution network system.
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