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1.
Sci Rep ; 13(1): 11372, 2023 07 14.
Article in English | MEDLINE | ID: mdl-37452108

ABSTRACT

Farmers' participation in food safety governance is an important part of food safety social co-governance, and the accurate identification of its influencing factors and their related paths is of guiding significance to the scientific decision-making of food safety governance. The system of influencing factors of farmers' participation in food safety governance was constructed from four dimensions, and the influence network of each dimension was revealed by decision laboratory analysis (DEMATEL). The hierarchical structure and correlation path of influencing factors were determined by interpretive structural model (ISM), and the attributes of influencing factors were further classified by cross influence matrix multiplication (MICMAC). The results show that the influencing factors of farmers' participation in food safety governance can be divided into seven levels, among which the level of education and the status of village cadres are the fundamental characteristic factors. The degree of rural informatization, the intensity of government supervision, the promotion of village committees, the response of the government and the degree of disclosure of government information are the deep core factors, and risk cognition, political trust and family eating habits are special factors. Taking the importance and attribute status of farmers' participation in food safety governance into decision-making considerations is of great significance to improve the efficiency of food safety governance.


Subject(s)
Agriculture , Farmers , Humans , Agriculture/methods , Trust , Food Safety , Cognition , China
2.
Adv Clin Exp Med ; 28(9): 1249-1255, 2019 09.
Article in English | MEDLINE | ID: mdl-31430071

ABSTRACT

BACKGROUND: The single-nucleotide polymorphisms (SNPs) of apurinic/apyrimidinicendonuclease 1 (APE1), which has been implicated in cancers and the DNA base excision repair (BER) process, have not been thoroughly investigated in association with the risks of oxidative stress-related vitiligo. OBJECTIVES: The aim of this study is to investigate associations between APE1 single-nucleotide polymorphisms 141T >G and 1349T >G and risk and prognosis of vitiligo. MATERIAL AND METHODS: From June 2013 to June 2015, a total of 460 vitiligo patients were randomly recruited as a case group; 200 of these patients received narrow bound ultraviolet B (NB-UVB) treatment. Meanwhile, 460 healthy controls were included as a control group. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was performed to explore the distribution frequencies of genotypes. RESULTS: Significant differences were detected between the case group and the control group in the frequencies of the 141T >G and 1349T >G genotypes. At 141T >G, compared with patients carrying the TG + GG genotype, male patients carrying the TT genotype aged more than 20 years with active non-segmental vitiligo, without a family history of vitiligo or other autoimmune diseases, exhibited an increased risk of vitiligo. Binary logistic regression analysis demonstrated that the TT genotype at 141T >G and the non-TT genotype at 1349T >G were independent risk factors for vitiligo development. At 1349T >G, compared with patients carrying the TT genotype, male patients carrying the TG + GG genotype aged more than 20 years with active non-segmental vitiligo, without a family history of vitiligo or other autoimmune diseases, exhibited an increased risk of vitiligo. Moreover, patients carrying 141TG + GG or 1349 TT genotypes had better photochromic effects, lower cumulative radiation doses, shorter treatment times, and earlier first photochromic times.


Subject(s)
Asian People/genetics , DNA-(Apurinic or Apyrimidinic Site) Lyase/metabolism , Polymorphism, Single Nucleotide , Vitiligo , Adult , Case-Control Studies , Female , Genetic Predisposition to Disease , Genotype , Humans , Male , Prognosis , Vitiligo/genetics , Vitiligo/metabolism , Young Adult
3.
J Cell Physiol ; 233(9): 7424-7434, 2018 09.
Article in English | MEDLINE | ID: mdl-29663367

ABSTRACT

Skin squamous cell carcinoma (SCC) is generally considered as nonaggressive lesions and mainly caused by ultraviolet (UV) radiation. Gadd45a is a key component protecting skin against UV-induced tumors. For that, the study aims to investigate the mechanism of Gadd45a gene silencing on cell proliferation, apoptosis, and senescence in nude mice with skin SCC through the p53 signaling pathway. Healthy nude mice was collected as the normal group and 40 nude mouse models of skin SCC were successfully established as the model group, which were sub-divided into five groups. The incidence, size, and weight of SCC tumor of nude mice were observed. The mRNA expression of Gadd45a, Cyclin B1, MMP-2, Bcl-2, and Bax were determined by RT-qPCR. Cell viability, cell cycle and apoptosis, cell senescence were detected by MTT assay, flow cytometry, and ß-galactosidase staining, respectively. The levels of inflammatory factors and vascular endothelial growth factor (VEGF) were detected by using ELISA. The protein expression rate of mutant p53 was detected by immunohistochemistry. Mice transfected with siGadd45a showed increased tumor incidence, size, and weight. Cells transfected with siGadd45a showed decrease in expression of Gadd45a and Bax; and increase in expression of Cyclin B1, MMP-2, and Bcl-2, expression of mutant p53, IL-1α, IL-1ß, IL-6, TNF-α, and VEGF. Cell apoptosis and senescence were inhibited, while cell viability and proliferation were promoted after siGadd45a treatment. The results reveal that Gadd45a silencing increases tumor cell proliferation and reduces apoptosis and senescence through the p53 signaling pathway in skin SCC.


Subject(s)
Apoptosis , Carcinoma, Squamous Cell/pathology , Cell Cycle Proteins/metabolism , Cellular Senescence , Nuclear Proteins/metabolism , RNA Interference , Signal Transduction , Skin Neoplasms/pathology , Tumor Suppressor Protein p53/metabolism , Animals , Carcinoma, Squamous Cell/genetics , Cell Line, Tumor , Cell Proliferation , Cell Survival , Cytokines/metabolism , Disease Progression , Humans , Lymphocytes/metabolism , Matrix Metalloproteinase 2/metabolism , Mice, Nude , Mutation/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Small Interfering/metabolism , S Phase , Skin Neoplasms/genetics , Tumor Burden , bcl-2-Associated X Protein/metabolism
4.
Biomed Pharmacother ; 90: 446-454, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28391166

ABSTRACT

The prostate cancer prognosis is still not fully understood. Chikusetsu saponin Iva (CHI), isolated from Aralia taibaiensis, shows anti-cancer and anti-inflammatory properties. Here, in our study, we attempted to explore the efficiency and the possible molecular mechanism by which CHI may suppress prostate cancer. CHI was found to inhibit prostate cancer cell proliferation and induce cell death without cytotoxicity in prostate normal cells. CHI resulted in intracellular reactive oxygen species (ROS) production, and induced apoptosis regulated by mitochondria in vitro studies. CHI-caused apoptosis was shown in both caspase-dependent and -independent manner, which released cyto-c, enhancing caspases expression and promoting apoptosis-inducing factors (AIF) as well as endonuclease G (Endo G) nuclear transfer, respectively. Moreover, in vivo study showed that prostate tumor was inhibited by CHI administration through apoptosis induction. Thus, the results illustrated that CHI might be an effective therapeutic strategy for prostate cancer treatment in future.


Subject(s)
Apoptosis/drug effects , Mitochondria/drug effects , Oleanolic Acid/analogs & derivatives , Prostatic Neoplasms/drug therapy , Saponins/pharmacology , Apoptosis Inducing Factor/metabolism , Caspases/metabolism , Cell Line, Tumor , Cell Proliferation/drug effects , Endodeoxyribonucleases/metabolism , Humans , Male , Mitochondria/metabolism , Oleanolic Acid/pharmacology , Prostatic Neoplasms/metabolism , Reactive Oxygen Species/metabolism , Signal Transduction/drug effects
5.
Mol Med Rep ; 14(4): 3735-42, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27571879

ABSTRACT

The present study aimed to explore the association between haptoglobin protein and mRNA expression and psoriasis. A total of 138 patients with psoriasis that were undergoing therapy at Linyi People's Hospital (Linyi, China) between January 2011 and January 2015 were enrolled in the present study. The mRNA expression levels of haptoglobin were detected by in situ hybridization; immunohistochemistry was used to detect haptoglobin protein expression; and double­labeling immunofluorescence was used to count Langerhans cells; western blotting was also conducted to determine protein expression. A receiver operating characteristic (ROC) curve was generated to assess the diagnostic value of haptoglobin for psoriasis. Compared with the normal and negative control (NC) groups, the mRNA expression levels of haptoglobin were markedly increased in the experimental group (P<0.05). Haptoglobin protein expression was also markedly increased in the experimental group compared with in the normal and NC groups (P<0.05). Conversely, there was no significant difference in haptoglobin expression between the NC group and the normal group (P>0.05). The critical value of haptoglobin mRNA in the diagnosis of psoriasis was 2.93, and sensitivity and specificity were 91.3 and 73.6%, respectively. The area under the ROC curve was 0.883 [95% confidence interval (CI)=0.837­0.929]. The critical value of haptoglobin protein in the diagnosis of psoriasis was 0.995, and sensitivity and specificity were 76.1 and 99.9%, respectively. The area under the ROC curve was 0.926 (95% CI=0.837­0.929). The present study demonstrated that the mRNA and protein expression levels of haptoglobin were increased in patients with psoriasis. Haptoglobin mRNA and protein expression were closely associated with the occurrence of psoriasis; therefore, haptoglobin may be considered a promising novel clinical indicator for the diagnosis of psoriasis.


Subject(s)
Haptoglobins/analysis , Haptoglobins/genetics , Psoriasis/genetics , RNA, Messenger/genetics , Skin/pathology , Adolescent , Adult , Aged , Female , Gene Expression , Humans , Male , Middle Aged , Psoriasis/diagnosis , Psoriasis/pathology , RNA, Messenger/analysis , ROC Curve , Young Adult
6.
Environ Sci Technol ; 41(15): 5505-9, 2007 Aug 01.
Article in English | MEDLINE | ID: mdl-17822124

ABSTRACT

This study was conducted to investigate the formation and destruction of NH3 during the gasification of coal in atmospheres containing O2 and steam. A Victorian brown coal was gasified in a novel bench-scale fluidized-bed/ fixed-bed reactor at 800 degrees C in atmospheres containing 2000 ppm O2, 15% H2O, or 2000 ppm O2 + 15% H2O. A NH3 standard gas was also used to study the destruction of NH3 in the gas phase and through gas-solid interactions. Sand, char, and coal ash were all found to enhance the destruction of NH3. An atmosphere containing O2 alone does not favor the conversion of char-N into NH3 but favors the destruction of NH3 through various mechanisms. The introduction of H2O into the gasification system greatly favors the conversion of char-N into NH3 and inhibits the destruction of NH3. The formation and destruction of NH3 in an atmosphere containing 15% H20 was similar to that in an atmosphere containing 15% H20 and 2000 ppm 02, indicating the dominant effects of steam in the formation and destruction of NH3 in a gasifier.


Subject(s)
Ammonia/chemistry , Coal , Oxygen/chemistry , Steam , Carbon/chemistry , Charcoal/chemistry , Coal Ash , Nitric Oxide/analysis , Particulate Matter/chemistry , Temperature , Time Factors
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