1.Role of copper metabolism in tumor development and tumor immunity
Liyan FU ; Qingxuan XIN ; Baohong YUE
Chinese Journal of Comparative Medicine 2025;35(5):131-138
Copper is an indispensable trace element that participates in numerous metabolic and signaling processes in both its oxidized and reduced states.It is intimately associated with several facets of tumor development,and alterations in copper homeostasis can substantially influence processes such as tumor cell growth,metastasis,modulation of the tumor microenvironment,oxidative stress,cell signaling,and the evasion of tumor cells from immune surveillance.Copper metabolism in tumor cells predominantly promotes immune escape by regulating the expression of programmed death ligand 1.In view of its crucial role in tumor immunity,modulating copper metabolism has emerged as a prospective therapeutic approach.This paper reviews the regulatory mechanisms of copper within the human body and investigates how disruptions to copper metabolism impact tumorigenesis and progression,along with the immune and tumor microenvironments.We also discuss the research value of copper as a target for tumor immunotherapy,thus providing a theoretical basis for future research and clinical applications.
2.Role of copper metabolism in tumor development and tumor immunity
Liyan FU ; Qingxuan XIN ; Baohong YUE
Chinese Journal of Comparative Medicine 2025;35(5):131-138
Copper is an indispensable trace element that participates in numerous metabolic and signaling processes in both its oxidized and reduced states.It is intimately associated with several facets of tumor development,and alterations in copper homeostasis can substantially influence processes such as tumor cell growth,metastasis,modulation of the tumor microenvironment,oxidative stress,cell signaling,and the evasion of tumor cells from immune surveillance.Copper metabolism in tumor cells predominantly promotes immune escape by regulating the expression of programmed death ligand 1.In view of its crucial role in tumor immunity,modulating copper metabolism has emerged as a prospective therapeutic approach.This paper reviews the regulatory mechanisms of copper within the human body and investigates how disruptions to copper metabolism impact tumorigenesis and progression,along with the immune and tumor microenvironments.We also discuss the research value of copper as a target for tumor immunotherapy,thus providing a theoretical basis for future research and clinical applications.
3.Expression of the hemagglutinin and neuramidinase gene of influenza A virus H1N1 in Pichia methanolica.
Ye ZHANG ; Zaijiang YU ; Li XIN ; Yongkun CHEN ; Qihui TANG ; Yubao CHEN ; Qingxuan CHEN ; Yuelong SHU
Chinese Journal of Biotechnology 2010;26(8):1068-1073
On the basis of successful cloning the full length hemagglulinin (HA) and neuramidinase (NA) gene and sequence analysis of influenza virus H1N1, part of the gene was ligated into pMETA. Expression vectors pMETA/HA (52-1 557 bp) and pMETA/NA (121-1 263 bp) were constructed and expressed in pMAD16 induced by methanol. Recombinant protein was purified through Ni2+ affinity chromatography. Western blotting and ELISA were used to determine the antigenic activity of the recombinant protein. SDS-PAGE showed that the recombinant capsid gene could be overexpressed in Pichia methanolica. ELISA and Western blotting showed that the recombinant protein had antigenicity.
Cloning, Molecular
;
Genetic Vectors
;
genetics
;
Hemagglutinins
;
biosynthesis
;
genetics
;
Influenza A Virus, H1N1 Subtype
;
genetics
;
Neuraminidase
;
biosynthesis
;
genetics
;
Pichia
;
genetics
;
metabolism
;
Recombinant Proteins
;
biosynthesis
;
genetics
;
immunology
4.A Novel Method to Transfer Gene In vivo System
Xin HE ; Bing QI ; Guisheng LIU ; Weidong YU ; Qingxuan CHEN
Progress in Biochemistry and Biophysics 2006;33(7):685-690
A new and effective method to produce transgenic animals was established. Without a surgical incision, the recombinant plasmid containing green fluorescence protein (GFP) cDNA was repeatedly injected into male mouse testis at multi-sites. After few weeks of the final injection, the injected male was mated with normal oestrus female to produce transgenic mice. The presence of the GFP cDNA in F1 transgenic individuals were detected by polymerase chain reaction and Southern blot hybridization, which showed that the transgenic rate of mouse F1 offspring was 41%. The transferred gene was integrated into the host genome and could be transmitted to its offspring. When the positive F1 individuals were mated with the wild type ICR mice, the F2 individuals had a transgenic rate of 37%. The results indicate that the high efficiency of gene transfer and the limited number of manipulations make the method suitable for creating a large number of transgenic animals, especially, for producing domestic animals.

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