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1.
Article in English | MEDLINE | ID: mdl-38551431

ABSTRACT

Objective: The objective of this study was to evaluate the effects of comfort care on perioperative outcomes and postoperative recovery of breast cancer patients. Evaluating comfort care is important in the context of breast cancer surgery because it can potentially alleviate pain, improve patient comfort, enhance postoperative recovery, and reduce complications, ultimately leading to better patient outcomes. Methods: Between March 2020 and December 2021, 78 patients undergoing breast cancer surgery at our hospital were randomly assigned to receive either routine nursing (routine group) or comfort care (experimental group). The comfort care intervention included various components such as health education, preoperative care, intraoperative care, postoperative care, pain care, and psychological care. The routine group received standard nursing care following medical advice. Results: The patient characteristics between the two groups were comparable. Comfort care resulted in significantly higher visual analog scale (VAS) scores, indicating reduced pain, and better improvement in functional recovery of the upper limb compared to routine nursing. Comfort care was also associated with better postoperative recovery, as evidenced by lower self-rating depression scale (SDS) and self-rating anxiety scale (SAS) scores. The experimental group had a significantly lower incidence of complications compared to the routine group. Additionally, the experimental group reported better 24-hour comfort and higher nursing satisfaction. Conclusion: In conclusion, comfort care effectively reduces postoperative pain, promotes postoperative recovery, improves patient emotions, lowers the incidence of complications, and enhances comfort and care satisfaction in breast cancer patients undergoing radical surgery. These findings highlight the importance of incorporating comfort care interventions in the perioperative management of breast cancer patients. Further research and implementation of comfort care strategies may have implications for improving clinical practice and patient outcomes in the future.

3.
Gastroenterol Rep (Oxf) ; 10: goac023, 2022.
Article in English | MEDLINE | ID: mdl-35686174

ABSTRACT

Background: Many studies have shown the operative feasibility and safety of robotic gastrectomy. Surgeons are pursuing single-port (SP) surgery to leverage the advantages of minimally invasive gastrectomy. The purpose of this study was to describe technical considerations and short-term outcomes from the first reported SP robotic total gastrectomy (RTG) using the da Vinci SP platform. Methods: A 75-year-old patient with a body-mass index of 19.8 kg/m2 and clinical stage III cancer (cT3N+M0) underwent SP RTG on 22 January 2022 at the Department of General Surgery, the Chinese PLA General Hospital. All procedures were performed successfully using the da Vinci SP robotic platform. Results: The SP RTG was successfully performed with D2 lymphadenectomy including No. 10 lymph-nodes dissection and extracorporeal Roux-en-Y anastomosis. Except for subcutaneous emphysema, no severe adverse events occurred during the operation. According to a visual analogue scale (VAS), the subjective feeling of post-operative pain was given a VAS score of 3 of 10 on Post-Operative Day 1 (POD 1), 1 of 10 on POD 3, and 1 of 10 on POD 7. We removed the gastric tube on POD 2 and advised sipping water, a liquid diet, and a soft diet on PODs 2, 4, and 6, respectively. The patient was discharged without any complications on POD 8. Conclusion: RTG is technically feasible and safe using the da Vinci SP robotic platform. To our knowledge, this is the first study using the da Vinci SP platform in RTG for advanced gastric cancer in elderly patients. To verify its superior operative outcomes, further clinical trials are needed.

4.
Pediatr Hematol Oncol ; 39(6): 549-560, 2022 Sep.
Article in English | MEDLINE | ID: mdl-35139734

ABSTRACT

Low expression of CTBP2 and CASP8AP2 correlated with poor outcome and predicted risk of relapse in pediatric B-cell acute lymphoblastic leukemia (B-ALL). This study aimed to investigate the molecular mechanism by which CASP8AP2 regulates LEF1 expression by interacting with CtBP2 and ZEB2 in Acute lymphoblastic lymphoma (ALL). There was an interaction between CASP8AP2, ZEB2, and CtBP2, and then the interaction between CtBP2 and ZEB2 was observed after downregulating the expression of CASP8AP2. The wild type (containing the ZEB2 binding site) or mutant (containing a mutant binding site) LEF1 gene promoter sequence was inserted into the pGL3-basic plasmid, and a dual-luciferase reporter gene detection system was used to observe how CASP8AP2, ZEB2, and CtBP2 regulate the transcription of the LEF1 gene. We conclude that CASP8AP2, CtBP2, and ZEB2 can all bind to the LEF1 gene promoter region and reduce the luciferase activity of the LEF1 promoter. Meanwhile, the interaction of ZEB2 and the LEF1 promoter was significantly weakened after downregulation of CASP8AP2. Knockdown of CASP8AP2 in the 697 cell lines resulted in the significant upregulation of the mRNA expression levels of the stemness-related genes CD44, JAG1, and SALL4. In conclusion, CASP8AP2 is vital for the interaction between CtBP2 and ZEB2, inhibiting LEF1 and stemness-related genes expression ALL.Supplemental data for this article is available online at https://doi.org/10.1080/08880018.2022.2033369 .


Subject(s)
Apoptosis Regulatory Proteins/metabolism , Calcium-Binding Proteins/metabolism , Co-Repressor Proteins/metabolism , Lymphoid Enhancer-Binding Factor 1/metabolism , Precursor Cell Lymphoblastic Leukemia-Lymphoma , Zinc Finger E-box Binding Homeobox 2/metabolism , Alcohol Oxidoreductases/genetics , Alcohol Oxidoreductases/metabolism , Apoptosis Regulatory Proteins/genetics , Calcium-Binding Proteins/genetics , Cell Line, Tumor , Child , Gene Expression , Humans , Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics , Transcription Factors/genetics
5.
Aging (Albany NY) ; 13(8): 11010-11025, 2021 02 01.
Article in English | MEDLINE | ID: mdl-33535179

ABSTRACT

Ultra-violet (UV) radiation (UVR) causes significant oxidative injury to retinal pigment epithelium (RPE) cells. Obacunone is a highly oxygenated triterpenoid limonoid compound with various pharmacological properties. Its potential effect in RPE cells has not been studied thus far. Here in ARPE-19 cells and primary murine RPE cells, obacunone potently inhibited UVR-induced reactive oxygen species accumulation, mitochondrial depolarization, lipid peroxidation and single strand DNA accumulation. UVR-induced RPE cell death and apoptosis were largely alleviated by obacunone. Obacunone activated Nrf2 signaling cascade in RPE cells, causing Keap1-Nrf2 disassociation, Nrf2 protein stabilization and nuclear translocation. It promoted transcription and expression of antioxidant responsive element-dependent genes. Nrf2 silencing or CRISPR/Cas9-induced Nrf2 knockout almost reversed obacunone-induced RPE cytoprotection against UVR. Forced activation of Nrf2 cascade, by Keap1 knockout, similarly protected RPE cells from UVR. Importantly, obacunone failed to offer further RPE cytoprotection against UVR in Keap1-knockout cells. In vivo, intravitreal injection of obacunone largely inhibited light-induced retinal damage. Collectively, obacunone protects RPE cells from UVR-induced oxidative injury through activation of Nrf2 signaling cascade.


Subject(s)
Benzoxepins/pharmacology , Limonins/pharmacology , Macular Degeneration/drug therapy , Oxidative Stress/drug effects , Retinal Pigment Epithelium/drug effects , Ultraviolet Rays/adverse effects , Animals , Apoptosis/drug effects , Apoptosis/radiation effects , Benzoxepins/therapeutic use , Cell Line , Cell Survival/drug effects , Cell Survival/radiation effects , DNA, Single-Stranded/drug effects , DNA, Single-Stranded/radiation effects , Disease Models, Animal , Drug Evaluation, Preclinical , Gene Expression Regulation/drug effects , Gene Knockout Techniques , Humans , Intravitreal Injections , Kelch-Like ECH-Associated Protein 1/metabolism , Limonins/therapeutic use , Lipid Peroxidation/drug effects , Lipid Peroxidation/radiation effects , Macular Degeneration/etiology , Macular Degeneration/pathology , Mice , Mitochondrial Membranes/drug effects , NF-E2-Related Factor 2/genetics , NF-E2-Related Factor 2/metabolism , Oxidative Stress/genetics , Oxidative Stress/radiation effects , Primary Cell Culture , Reactive Oxygen Species/metabolism , Retinal Pigment Epithelium/cytology , Retinal Pigment Epithelium/pathology , Retinal Pigment Epithelium/radiation effects , Signal Transduction/drug effects , Signal Transduction/genetics , Signal Transduction/radiation effects
6.
Andrologia ; 53(4): e14005, 2021 May.
Article in English | MEDLINE | ID: mdl-33565168

ABSTRACT

This study evaluates the protective role of oyster peptide (OP) on the occurrence of Exercise-Hypogonadal Male Condition. Male rats were given heavy-load swimming training and / or OP was supplemented for 6 consecutive weeks. After heavy-load training, sperm count, sperm viability and sperm motility in epididymis, testosterone in serum and testis, glutathione peroxidase (GSH-px) and androgen receptor (AR) in testis and mating times were remarkably decreased, malondialdehyde (MDA), capture latency and mating latency were significantly increased, mRNA expression of steroidogenic acute regulatory (StAR) and P450 cholesterol side-chain cleavage enzyme (P450scc) were obviously down-regulated, but serum follicle-stimulating hormone (FSH) and luteinising hormone (LH) were not statistically changed. Conversely, when OP was supplemented at heavy-load training, sperm count, sperm viability and sperm motility in epididymis, serum FSH, LH, testosterone, GSH-px, superoxide dismutase (SOD), testosterone, AR in testis and mating times were dramatically increased, while testicular MDA, capture latency and mating latency were significantly decreased, and mRNA expression of StAR, StARD7, P450scc and 3ß-hydroxysteroid dehydrogenase (3ß-HSD) were significantly up-regulated. In conclusion, heavy-load training causes testicular spermatogenic and steroidogenic disorders by enhancing the generation of reactive oxygen species (ROS), which can be protected by the co-administration of OP by enhancing the function of pituitary gonad axis and lowering ROS generation.


Subject(s)
Ostreidae , Sperm Motility , Animals , Carrier Proteins , Luteinizing Hormone , Male , Rats , Sperm Count , Testis , Testosterone
7.
Am J Med Sci ; 360(6): 701-710, 2020 12.
Article in English | MEDLINE | ID: mdl-33012486

ABSTRACT

BACKGROUND: Lung squamous cell carcinoma (LUSC) accounts up for approximately 30% of all lung cancers with a high mortality. The study was aimed at finding genes critical in the diagnosis and prognosis of LUSC. MATERIALS AND METHODS: The differentially expressed (DE) genes (DEGs) and DE lncRNAs (DELs) from 501 LUSC and 49 normal lung tissues, and DE miRNAs (DEMs) from 478 LUSC and 45 normal lung tissues were respectively obtained via the TCGA database. Gene ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway, and co-expression network analyses were performed. Survival analysis and receiver operating characteristic curve of hub mRNAs were also analyzed. Competitive endogenous RNA networks of lncRNAs, miRNAs and mRNAs were constructed. RESULTS: A total of 5747 DEGs, 378 DEMs and 3141 DELs in LUSC were identified in LUSC. The DEGs including AUARK, CDK1, KIF11 and EXO1 were proven to be significant metastatic indicators in LUSC, and 2 DEGs were significantly associated with the survival in LUSC patients. Some genes might have connections with many other gene nodes through a co-expression network. Four lncRNAs, 2 mRNAs and 2 miRNAs were identified as the candidates for the competitive miRNA-mRNA-lncRNA network and might serve as prognostic markers in LUSC. CONCLUSIONS: We identified the differentially expressed lncRNAs, miRNAs and mRNAs in LUSC, providing further insights into the molecular mechanism of LUSC tumorigenesis and the potential prognostic biomarkers or therapeutic targets for LUSC.


Subject(s)
Carcinoma, Squamous Cell/genetics , Gene Expression Regulation, Neoplastic , Lung Neoplasms/genetics , MicroRNAs/metabolism , RNA, Long Noncoding/metabolism , RNA, Messenger/metabolism , Carcinoma, Squamous Cell/diagnosis , Gene Ontology , Gene Regulatory Networks , Humans , Lung , Lung Neoplasms/diagnosis , Prognosis , ROC Curve , Survival Analysis
8.
Curr Top Med Chem ; 20(10): 835-846, 2020.
Article in English | MEDLINE | ID: mdl-32141418

ABSTRACT

BACKGROUND: Although the involvement of individual microRNA and lncRNA in the regulation of p21 expression has largely been evidenced, less is known about the roles of functional interactions between miRNAs and lncRNAs in p21 expression. Our previous work demonstrated that miR-509- 3-5p could block cancer cell growth. METHODS: To gain an insight into the role of miR-509-3-5p in the regulation of p21 expression, we performed in silico prediction and showed that miR-509-3-5p might target the NONHSAT112228.2, a sense-overlapping lncRNA transcribed by a non-code gene overlapping with p21 gene. Mutation and luciferase report analysis suggested that miR-509-3-5p could target NONHSAT112228.2, thereby blocking its expression. Consistently, NONHSAT112228.2 expression was inversely correlated with both miR-509-3-5p and p21 expression in cancer cells. Ectopic expression of miR-509-3-5p and knockdown of NONHSAT112228.2 both promoted proliferation and migration of cancer cells. RESULTS: Interestingly, high-expression of NONHSAT112228.2 accompanied by low-expression of p21 was observed in lung cancer tissues and associated with lower overall survival. CONCLUSION: Taken together, our study found a new regulatory pathway of p21, in which MiR-509-3-5p functionally interacts with NONHSAT112228.2 to release p21 expression. MiR-509-3-5p- NONHSAT112228.2 regulatory axis can inhibit the proliferation and migration of lung cancer cells.


Subject(s)
Carcinoma, Non-Small-Cell Lung/metabolism , Cyclin-Dependent Kinase Inhibitor p21/genetics , Lung Neoplasms/metabolism , MicroRNAs/metabolism , Mutant Proteins/genetics , Amino Acid Sequence , Cell Line, Tumor , Cell Movement , Cell Proliferation , Computational Biology , Computer Simulation , Cyclin-Dependent Kinase Inhibitor p21/metabolism , Gene Expression Regulation, Neoplastic , Gene Knockdown Techniques , Humans , Luciferases/genetics , Luciferases/metabolism , Mutant Proteins/chemistry , Mutant Proteins/metabolism , Mutation , RNA, Long Noncoding/metabolism , Transfection , Wound Healing/drug effects
9.
Insect Sci ; 27(4): 675-686, 2020 Aug.
Article in English | MEDLINE | ID: mdl-30912872

ABSTRACT

During insect larval-pupal metamorphosis, proteins in the hemolymph are absorbed by the fat body for the maintenance of intracellular homeostasis; however, the type of proteins and how these proteins are internalized into the fat body are unclear. In Bombyx mori, the developmental profiles of total proteins in the hemolymph and fat body showed that hemolymph-decreased protein bands (55-100 kDa) were in accordance with those protein bands that increased in the fat body. Inhibition of clathrin-dependent endocytosis predominantly blocked the transportation of 55-100 kDa proteins from the hemolymph into the fat body, which was further verified by RNA interference treatment of Bmclathrin. Six hexamerins were shown to comprise ∼90% of the total identified proteins in both the hemolymph and fat body by mass spectrum (MS) analysis. In addition, hemolymph-specific proteins were mainly involved in material transportation, while fat body-specific proteins particularly participated in metabolism. In this paper, four hexamerins were found for the first time, and potential proteins absorbed by the fat body from the hemolymph through clathrin-dependent endocytosis were identified. This study sheds light on the protein absorption mechanism during insect metamorphosis.


Subject(s)
Bombyx/physiology , Clathrin/metabolism , Endocytosis , Fat Body/physiology , Hemolymph/physiology , Insect Proteins/metabolism , Absorption, Physiological , Animals , Bombyx/growth & development , Larva/growth & development , Larva/physiology
10.
J Dig Dis ; 21(1): 46-51, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31794121

ABSTRACT

OBJECTIVE: The prevalence of inflammatory bowel disease (IBD) has been increasing worldwide, and the risk of infection has increased due to the use of immunosuppressive and biologic medications. Some of these infections can be prevented with vaccinations. The aim of this study was to evaluate the vaccination practices of Chinese gastroenterologists for patients with IBD. METHODS: Questionnaires based on quick response codes were sent using email and the WeChat platform to gastroenterologists at 20 hospitals in China. The vaccination practices of the gastroenterologists, including vaccinating for hepatitis B, hepatitis A, and varicella, were assessed. RESULTS: Of the 468 gastroenterologists who received the questionnaire, 307 (65.6%) completed it. Of the gastroenterologists who were most concerned about hepatitis B; 83.4% always or frequently asked about an infection history, 53.7% took an immunization history, and 73.6% tested patients for hepatitis B infection. However, few gastroenterologists did so for hepatitis A or varicella. The proportion of patients who were asked about an infection and immunization history and tested for varicella infection was 16.0%, 15.0%, and 9.4%, respectively. Only a few gastroenterologists recommended vaccination for patients without an infection before IBD medical treatment (26.7% for hepatitis A, 45.6% for hepatitis B, and 28% for varicella vaccination). CONCLUSION: Vaccination practices for patients with IBD used by Chinese gastroenterologists vary greatly, suggesting that education about immunization is needed.


Subject(s)
Gastrointestinal Agents/adverse effects , Hepatitis, Viral, Human/prevention & control , Inflammatory Bowel Diseases/therapy , Vaccination , Varicella Zoster Virus Infection/prevention & control , Viral Vaccines/therapeutic use , Biological Products/adverse effects , Biological Products/therapeutic use , Chickenpox Vaccine/therapeutic use , China/epidemiology , Female , Gastroenterology/statistics & numerical data , Gastrointestinal Agents/therapeutic use , Health Care Surveys , Health Knowledge, Attitudes, Practice , Hepatitis A Vaccines/therapeutic use , Hepatitis B Vaccines/therapeutic use , Hepatitis, Viral, Human/etiology , Humans , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/therapeutic use , Inflammatory Bowel Diseases/complications , Inflammatory Bowel Diseases/epidemiology , Male , Professional Practice/statistics & numerical data , Vaccination/statistics & numerical data , Varicella Zoster Virus Infection/etiology , Viral Hepatitis Vaccines/therapeutic use
11.
Clin Hemorheol Microcirc ; 71(1): 3-8, 2019.
Article in English | MEDLINE | ID: mdl-29660902

ABSTRACT

OBJECTIVE: This study aims to study the effect of Rho kinase inhibitor fasudil on the expression endothelin-1 (ET-1) and nitric oxide (NO) in rats with hypoxic pulmonary hypertension (HPH). METHODS: Twenty-four male SD rats were randomly divided into three groups: control group, model group (HPH group) and HPH+fasudil group. The rat HPH model was established by intermittent hypoxia (IH) at atmospheric pressure. Mean pulmonary artery pressure (mPAP), right ventricular hypertrophy index (RVHI), ET-1 and NO levels, and pulmonary vascular structural changes were observed in all groups. RESULTS: MPAP, RVHI and ET-1 levels were significantly higher in HPH group than in control group, while NO was significantly lower than in control group. In addition, mPAP, RVHI and ET-1 were significantly lower in the HPH+fasudil group than in the HPH group. In the HPH group, ET-1 level was significantly and positively correlated with mPAP and RVHI, NO was negatively correlated with mPAP and RVHI levels, and ET-1 level was significantly and negatively correlated with NO level. In the HPH group, pulmonary arteriolar walls were generally thickened, and lumen stenosis was obvious; while after fasudil treatment, pulmonary arteriolar wall thickening and stenosis degree were significantly reduced. CONCLUSION: Fasudil can significantly reduce ET-l level and increase NO level in HPH rats, suppressing the development of pulmonary arterial hypertension.


Subject(s)
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/analogs & derivatives , Endothelin-1/metabolism , Hypertension, Pulmonary/drug therapy , Nitric Oxide/metabolism , Protein Kinase Inhibitors/therapeutic use , 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/pharmacology , 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/therapeutic use , Animals , Disease Models, Animal , Hypertension, Pulmonary/pathology , Male , Protein Kinase Inhibitors/pharmacology , Rats , Rats, Sprague-Dawley
12.
Biochem Biophys Res Commun ; 506(1): 73-80, 2018 11 17.
Article in English | MEDLINE | ID: mdl-30340831

ABSTRACT

AMP-activated protein kinase (AMPK) signaling activation can inhibit Ultra-violet (UV) radiation (UVR)-induced retinal pigment epithelium (RPE) cell injuries. LB-100 is a novel inhibitor of protein phosphatase 2A (PP2A), the AMPKα1 phosphatase. Here, our results demonstrated that LB-100 significantly inhibited UVR-induced viability reduction, cell death and apoptosis in established ARPE-19 cells and primary murine RPE cells. LB-100 activated AMPK, nicotinamide adenine dinucleotide phosphate (NADPH) and Nrf2 (NF-E2-related factor 2) signalings, inhibiting UVR-induced oxidative injuries and DNA damage in RPE cells. Conversely, AMPK inhibition, by AMPKα1-shRNA, -CRISPR/Cas9 knockout or -T172A mutation, almost blocked LB-100-induced RPE cytoprotection against UVR. Importantly, CRISPR/Cas9-mediated PP2A knockout mimicked and nullified LB-100-induced anti-UVR activity in RPE cells. Collectively, these results show that PP2A inhibition by LB-100 protects RPE cells from UVR via activation of AMPK signaling.


Subject(s)
AMP-Activated Protein Kinases/genetics , Bridged Bicyclo Compounds, Heterocyclic/pharmacology , Enzyme Inhibitors/pharmacology , Epithelial Cells/drug effects , Piperazines/pharmacology , Protein Phosphatase 2/genetics , Sunscreening Agents/pharmacology , AMP-Activated Protein Kinases/metabolism , Animals , CRISPR-Cas Systems , Cell Line , Cell Survival/drug effects , Cell Survival/radiation effects , Enzyme Activation , Epithelial Cells/cytology , Epithelial Cells/metabolism , Epithelial Cells/radiation effects , Gene Editing , Gene Expression Regulation , Humans , Mice , NADP/metabolism , Primary Cell Culture , Protein Phosphatase 2/antagonists & inhibitors , Protein Phosphatase 2/metabolism , RNA, Small Interfering/genetics , RNA, Small Interfering/metabolism , Reactive Oxygen Species/metabolism , Retinal Pigment Epithelium/cytology , Retinal Pigment Epithelium/drug effects , Retinal Pigment Epithelium/metabolism , Retinal Pigment Epithelium/radiation effects , Signal Transduction , Ultraviolet Rays/adverse effects
13.
Int J Mol Sci ; 19(6)2018 May 28.
Article in English | MEDLINE | ID: mdl-29843366

ABSTRACT

Human lung cancer H1299 (p53-null) cells often display enhanced susceptibility to chemotherapeutics comparing to A549 (p53-wt) cells. However, little is known regarding to the association of DNA damage-response (DDR) pathway heterogeneity with drug sensitivity in these two cells. We investigated the DDR pathway differences between A549 and H1299 cells exposed to 8-chloro-adenosine (8-Cl-Ado), a potential anticancer drug that can induce DNA double-strand breaks (DSBs), and found that the hypersensitivity of H1299 cells to 8-Cl-Ado is associated with its DSB overaccumulation. The major causes of excessive DSBs in H1299 cells are as follows: First, defect of p53-p21 signal and phosphorylation of SMC1 increase S phase cells, where replication of DNA containing single-strand DNA break (SSB) produces more DSBs in H1299 cells. Second, p53 defect and no available induction of DNA repair protein p53R2 impair DNA repair activity in H1299 cells more severely than A549 cells. Third, cleavage of PARP-1 inhibits topoisomerase I and/or topoisomerase I-like activity of PARP-1, aggravates DNA DSBs and DNA repair mechanism impairment in H1299 cells. Together, DDR pathway heterogeneity of cancer cells is linked to cancer susceptibility to DNA damage-based chemotherapeutics, which may provide aid in design of chemotherapy strategy to improve treatment outcomes.


Subject(s)
2-Chloroadenosine/analogs & derivatives , Antineoplastic Agents/pharmacology , DNA Breaks, Double-Stranded/drug effects , DNA Repair/drug effects , DNA, Neoplasm/genetics , Gene Expression Regulation, Neoplastic/drug effects , 2-Chloroadenosine/pharmacology , A549 Cells , Cell Cycle Proteins/genetics , Cell Cycle Proteins/metabolism , Cell Line, Tumor , Chromosomal Proteins, Non-Histone/genetics , Chromosomal Proteins, Non-Histone/metabolism , Cyclin-Dependent Kinase Inhibitor p21/genetics , Cyclin-Dependent Kinase Inhibitor p21/metabolism , DNA Replication , DNA Topoisomerases, Type I/genetics , DNA Topoisomerases, Type I/metabolism , DNA, Neoplasm/metabolism , Humans , Organ Specificity , Phosphorylation , Poly (ADP-Ribose) Polymerase-1/genetics , Poly (ADP-Ribose) Polymerase-1/metabolism , Signal Transduction , Tumor Suppressor Protein p53/genetics , Tumor Suppressor Protein p53/metabolism
14.
Proteins ; 85(12): 2231-2238, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28921635

ABSTRACT

Protein phosphorylation is one of the most pervasive post-translational modifications and regulates diverse cellular processes in organisms. Under the catalysis of protein kinases, protein phosphorylation usually occurred in the residues serine (S), threonine (T), or tyrosine (Y). In this contribution, we proposed a novel scheme (named KMPhos) for the theoretical prediction of protein phosphorylation sites. First, the numerical matrix was obtained from a protein sequence fragment by replacing the characters of the residues with the chemical descriptors of amino acid molecules to approximately describe the chemical environment of the protein fragment, which was turned to the grayscale image. Then the Krawtchouk image moments were calculated and used to establish the support vector machine models. The accuracies of 10-fold cross validation for the obtained models on the training set are up to 89.7%, 88.6%, and 90.1% for the residues S, Y, and T, respectively. For the independent test set, the prediction accuracies are up to 90.7% (S), 87.8% (T), and 89.3% (Y). The results of ROC and other evaluations are also satisfactory. Compared with several specialized prediction tools, KMPhos provided the higher accuracy and reliability. An available KMPhos package is provided and can be used directly for phosphorylation sites prediction.


Subject(s)
Arabidopsis Proteins/metabolism , Arabidopsis/metabolism , Protein Processing, Post-Translational , Serine/metabolism , Threonine/metabolism , Tyrosine/metabolism , Amino Acid Sequence , Arabidopsis/genetics , Arabidopsis Proteins/genetics , Area Under Curve , Computational Biology/methods , Phosphorylation , Protein Kinases/genetics , Protein Kinases/metabolism , ROC Curve , Support Vector Machine
15.
Ying Yong Sheng Tai Xue Bao ; 28(3): 911-917, 2017 Mar 18.
Article in Chinese | MEDLINE | ID: mdl-29741019

ABSTRACT

The main wheat production area in Henan Province was classified into five regions based on observed wheat production data, historical meteorological data and soil data from thirty sites du-ring 1981 to 2014. The changes in the risk of yield loss of winter wheat under water stress condition in each region were calculated with WOFOST model. From 1981 to 2014, the yield reduction rate of winter wheat showed an increasing trend at all the sites with the increase rate of 2.8%-5.0% per 10 years. The yield reduction rate decreased from north to south in Henan Province. The event of yield reduction rate over 20% occurred about once every 10 years in southern Henan Province, and once every 2 years at Xinxiang, Fengqiu and Puyang in northern Henan Province. The event of yield reduction rate over 50% occurred about once every 3 years at Xinxiang and Zhengzhou but was rare in southern Henan Province. The highest hazard areas were mainly distributed in north and middle parts of Henan Province, the lowest hazard areas were distributed at Lushi in western Henan Pro-vince, Nanyang in southwestern Henan Province, Xinyang in southern Henan Province and south part of Zhumadian, the medium hazard areas were distributed in the other regions of Henan Province.


Subject(s)
Dehydration , Triticum , China , Seasons , Water
16.
Biochem Biophys Res Commun ; 478(2): 676-82, 2016 09 16.
Article in English | MEDLINE | ID: mdl-27498003

ABSTRACT

MicroRNAs (miRNAs) are potent post-transcriptional regulators of gene expression and play roles in DNA damage response (DDR). PLK1 is identified as a modulator of DNA damage checkpoint. Although down-regulation of PLK1 by certain microRNAs has been reported, little is known about the interplay between PLK1 and miR-509-3-5p in DDR. Here we have demonstrated that miR-509-3-5p repressed PLK1 expression by targeting PLK1 3'-UTR, thereby causing mitotic aberration and growth arrest of human lung cancer A549 cells. Repression of PLK1 by miR-509-3-5p was further evidenced by over-expression of miR-509-3-5p in A549, HepG2 and HCT116p53(-/-) cancer cells, in which PLK1 protein was suppressed. Consistently, miR-509-3-5p was stimulated, while PLK1 protein was down-regulated in A549 cells exposed to CIS and ADR, suggesting that suppression of PLK1 by miR-509-3-5p is a component of CIS/ADR-induced DDR pathway. Flow cytometry and immunofluorescence labeling showed that over-expression of miR-509-3-5p in A549 induced G2/M arrest and aberrant mitosis characterized by abnormal bipolar mitotic spindles, condensed chromosomes, lagging DNA and chromosome bridges. In addition, over-expression of miR-509-3-5p markedly blocked A549 cell proliferation and sensitized the cells to CIS and ADR treatment. Taken together, miR-509-3-5p is a feasible suppressor for cancer by targeting PLK1. Our data may provide aid in potential design of combined chemotherapy and in our better understanding of the roles of microRNAs in response to DNA damage.


Subject(s)
Cell Cycle Proteins/genetics , Gene Expression Regulation, Neoplastic , MicroRNAs/genetics , Protein Serine-Threonine Kinases/genetics , Proto-Oncogene Proteins/genetics , 3' Untranslated Regions , A549 Cells , Antibiotics, Antineoplastic/pharmacology , Apoptosis/drug effects , Base Sequence , Cell Cycle Proteins/antagonists & inhibitors , Cell Cycle Proteins/metabolism , Cell Proliferation/drug effects , Cisplatin/pharmacology , Doxorubicin/pharmacology , G2 Phase Cell Cycle Checkpoints/drug effects , HCT116 Cells , Hep G2 Cells , Humans , MicroRNAs/metabolism , Mitosis/drug effects , Protein Serine-Threonine Kinases/antagonists & inhibitors , Protein Serine-Threonine Kinases/metabolism , Proto-Oncogene Proteins/antagonists & inhibitors , Proto-Oncogene Proteins/metabolism , Signal Transduction , Polo-Like Kinase 1
17.
Sensors (Basel) ; 16(6)2016 Jun 21.
Article in English | MEDLINE | ID: mdl-27338401

ABSTRACT

To balance energy consumption and reduce latency on data transmission in Wireless Sensor Networks (WSNs), a type of low-latency data gathering method with multi-Sink (LDGM for short) is proposed in this paper. The network is divided into several virtual regions consisting of three or less data gathering units and the leader of each region is selected according to its residual energy as well as distance to all of the other nodes. Only the leaders in each region need to communicate with the mobile Sinks which have effectively reduced energy consumption and the end-to-end delay. Moreover, with the help of the sleep scheduling and the sensing radius adjustment strategies, redundancy in network coverage could also be effectively reduced. Simulation results show that LDGM is energy efficient in comparison with MST as well as MWST and its time efficiency on data collection is higher than one Sink based data gathering methods.

18.
Ying Yong Sheng Tai Xue Bao ; 26(8): 2405-13, 2015 Aug.
Article in Chinese | MEDLINE | ID: mdl-26685604

ABSTRACT

Surveying data for wind lodging disaster happening in Nanyang of Henan Province in August 1, 2013, were used to analyze the effects of strong wind lodging at pre- and post-tasseling stages on growth and yield of summer maize, and to determine the differences in lodging resistance among varieties and the suitable sowing time for summer maize. The survey included two varieties of summer maize, Xundan 20 and Zhengdan 958, with five and three sowing dates, respectively. The lodging was divided into four types, i.e., root slope ( RS) , root lodging ( RL) , stem bending (SB) and stem broken (SBK). The results showed that wind lodging occurring at pre- and post-tasseling stages resulted in high lodging percentages for both varieties and all sowing dates. The lodging percentage of Xundan 20 variety ranged between 86.0% and 98.5% for five sowing dates. For Zhengdan 958 variety, it ranged between 60.0% and 76.4% for three sowing dates. After tasseling, the earlier the sowing date, the lower the lodging rate occurred. The main lodging types happening around the tasseling stage were RL with the lodging rate of 53.0%-84.3% for sowing dates II-V of Xundan 20. The main lodging type for sowing date I was SB with the lodging rate of 37.5%. Lodging reduced the aboveground dry matter with the greatest reduction rate occurring in SB, followed by RS and RL. Lodging increased the allocation of dry matter to leaves and stems, but decreased the allocation to spikes. RL and SB shortened the length and diameter of spike, and reduced the grain number per spike. The lodging occurring after the tasseling stage also reduced 100-grain mass. RS had no significant effects on spike characters and yield components. The lodging had serious effects on the yield of summer maize. The yield loss was highest for SB with the reduction percentages of 74.2% and 68.7% for Xundan 20 and Zhengdan 958, respectively. SB occurring before the tasseling stage would lead to a complete crop failure. RL decreased the average yield by 46.3% and 46.5% for Xundan 20 and Zhengdan 958, respectively. RS decreased the averaged yield by 8.4% and 13.2% for Xundan 20 and Zhengdan 958, respectively. The mean yields of Xundan 20 and Zhengdan 958 were 4959.9 and 6026.1 kg · hm(-2) after the wind lodging, respectively. The later the sowing date, the higher the yield loss rate was observed for Xundan 20, however, there were no significant difference in yield loss among different sowing dates of Zhengdan 958. In general, Zhengdan 958 had stronger lodging resistance than Xundan 20.


Subject(s)
Wind , Zea mays/growth & development , Plant Leaves/growth & development , Plant Stems/growth & development
19.
Int J Clin Exp Pathol ; 8(8): 9517-21, 2015.
Article in English | MEDLINE | ID: mdl-26464714

ABSTRACT

OBJECTIVE: To investigate whether right ventricular hypertrophy in hypoxic pulmonary hypertension (HPH) rats could be prevented by treatment with Rho kinase inhibitor fasudil. METHODS: The rat model of pulmonary hypertension was established by exposing rats to normobaric intermitent hypoxia [(10 ± 0.5)% O2]. Twenty-four Spraque-Dawley male rats were randomly divided into control group, hypoxic model group and hypoxia with fasudil groups (n=8 each). The mean pulmonary arterial pressure (mPAP), and right ventricle hypertrophy index (RVHI) were measured. Ultrastructure of the right ventricular myocardial cells was observed under transmission electron microscope (TEM). - RESULTS: The level of mPAP (31.38 ± 1.98) mmHg and RVHI (0.47 ± 0.03) were significantly higher in the hypoxic model group than (15.25 ± 0.91) mmHg and (0.25 ± 0.02) in control group respectively (P<0.01). Transmission electron microscope (TEM) revealed the model group right ventricular mitochondria increased significantly, swelling, cristae blurred, lost, heart muscle Siming dark band was not clear. The level of mPAP (16.63 ± 1.53) mmHg and RVHI (0.27 ± 0.02) were significantly lower in fasudil treatment group than in model group respectively (P<0.01). After the intervention of fasudil right ventricular myocardial injury was significantly reduced. CONCLUSIONS: Fasudil may partly prevent and reverse the development of pulmonary hypertension and right ventricular hypertrophy and myocardial cell injury.


Subject(s)
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/analogs & derivatives , Hypertension, Pulmonary/pathology , Hypertrophy, Right Ventricular/pathology , Protein Kinase Inhibitors/pharmacology , 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/pharmacology , Animals , Disease Models, Animal , Heart/drug effects , Hypoxia/complications , Male , Microscopy, Electron, Transmission , Myocardium/ultrastructure , Rats , Rats, Sprague-Dawley
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