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Clinical importance of PCA3 lncRNA Aberrant expression in chronic myeloid leukemia patients: a comparative method PCA3 lncRNA异常表达在慢性髓性白血病患者中的临床意义:一种比较方法
Pub Date : 2023-08-09 DOI: 10.1515/tjb-2021-0114
Ling He, Jie Zhang, Yang Peng, Hongwei Wu, Zhiqiang Sun
Abstract Objectives Long noncoding RNAs (lncRNAs) plays important role in disease spread and its invasion. Overexpression of prostate cancer antigen 3 gene (PCA3gene) is reported in prostate cancer. To analyze the PCA3 lncRNA expression in chronic myeloid leukemia (CML) patients. Methods The study included clinically confirmed 100 CML patients and 100 healthy subjects. Relative quantification using Sybr Green dye was used to calculate the PCA3 lncRNAs expression. Total RNA was extracted by TRIzol method and quantitative real-time polymerase chain reaction. Results In CML patients, 9.96 ± 4.77-folds increased noncoding PCA3 lncRNA expression was observed compared to healthy subjects. Patients of chronic phase, accelerated phase, and blast crisis phase had 4.46 ± 1.36, 7.31 ± 3.10, and 12.91 ± 4.85-fold PCA3 lncRNA expression compared to healthy subjects (p<0.0001), respectively. CML patients who have a complaint of splenomegaly had higher PCA3 lncRNA expression than those who did not complain splenomegaly compared to healthy subjects (12.04 ± 5.02-fold vs. 6.09 ± 3.39-fold, p<0.0001). Patients who had ≤20,000 TLC showed fewer PCA3 lncRNA expression than those who had >20 thousand of TLC (4.45 ± 1.84 vs. 11.25 ± 5.05, p<0.0001). Receiver operating characteristic showed correlation of PCA3 lncRNA expression with severity of cancer. Conclusions lncRNA PCA3 expression to be linked with different stages of the disease and a prognostic indicator for disease in CML patients.
【摘要】目的长链非编码rna (Long noncoding rna, lncRNAs)在疾病传播和侵袭过程中发挥重要作用。前列腺癌抗原3基因(pca3基因)在前列腺癌中有过表达的报道。目的分析慢性髓性白血病(CML)患者PCA3 lncRNA的表达。方法选取临床确诊的CML患者100例和健康对照者100例。采用Sybr Green染色相对定量法计算PCA3 lncRNAs的表达。采用TRIzol法和实时定量聚合酶链反应提取总RNA。结果在CML患者中,非编码PCA3 lncRNA的表达比健康人群增加了9.96±4.77倍。慢性期、加速期和母细胞危亡期患者PCA3 lncRNA表达量分别为健康者的4.46±1.36、7.31±3.10和12.91±4.85倍(TLC p2万)(4.45±1.84∶11.25±5.05,p<0.0001)。受体工作特征显示PCA3 lncRNA表达与肿瘤严重程度相关。结论lncRNA PCA3的表达可能与CML患者疾病的不同分期有关,是CML患者疾病的预后指标。
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引用次数: 0
Examining the views of student midwives and nurses on biochemistry education 调查学生助产士和护士对生物化学教育的看法
Pub Date : 2023-08-09 DOI: 10.1515/tjb-2022-0137
Veysel Tahiroğlu
Abstract Objectives The aim of this study is to determine the opinions of midwives and nurses about the efficiency and effectiveness of the biochemistry courses they took during their undergraduate education, in the education process and in their fields of study. Methods Two hundred eighty-four students studying in the department of midwifery and nursing (1–4 classes) participated in this research voluntarily. A questionnaire consisting of 10 multiple-choice questions compiled by the authors with the support of the sociodemographic data form, including age, gender, type of lycee school graduated, and the department they studied, and the literature on biochemistry education were applied to the students. Results The mean age of the students was 21.25 ± 0.12. 58.2 % of midwifery department students and 69.1 % of nursing department students reported that biochemistry education is necessary. 64.1 % of midwifery department students and 59.7 % of nursing department students stated that they thought that the biochemistry application course should be absolutely necessary. There was a significant difference between nursing and midwifery students in favor of nursing students in terms of finding the biochemistry course interesting and loving the biochemistry course. A significant difference was found between the two groups in favor of midwifery students in terms of their desire to pursue postgraduate education in biochemistry and to increase biochemistry course hours (p<0.05). Conclusions It is thought that the results of this study, which include students’ opinions, will contribute to the efficiency of biochemistry education and help the lecturer provide a new perspective.
摘要目的本研究旨在了解助产士和护士对本科生物化学课程学习的效率和效果、学习过程和专业的看法。方法284名产护系(1-4班)学生自愿参与本研究。本研究以社会人口学资料表为基础,编制了包括年龄、性别、毕业中学类型、专业等10道选择题的问卷,并参考了生物化学教育方面的文献资料。结果学生平均年龄为21.25±0.12岁。58.2% %的助产系学生和69.1% %的护理系学生认为有必要进行生物化学教育。64.1 %的助产系学生和59.7 %的护理系学生认为生物化学应用课程是绝对必要的。护生对生物化学课程的兴趣程度、对生物化学课程的热爱程度在护生与助产学生之间存在显著差异。助产生对生物化学研究生学习意愿和增加生物化学学时意愿两组差异有统计学意义(p<0.05)。本研究的结果,包括学生的意见,将有助于提高生物化学教学的效率,并帮助讲师提供新的视角。
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引用次数: 0
Gingival status and prophylactic oral hygiene measures modulate salivary amino acids’ profile in children with plaque-induced gingivitis 牙龈状况和预防性口腔卫生措施可调节牙菌斑性牙龈炎儿童唾液氨基酸的分布
Pub Date : 2023-08-09 DOI: 10.1515/tjb-2023-0107
B. Galunska, A. Salim, M. Nikolova, S. Angelova, Y. Kiselova-Kaneva, S. Peev, D. Ivanova
Abstract Objectives Plaque-induced gingivitis is one of the most widely distributed periodontal disorder during childhood. The control of the pathogenic potential of the plaque is associated with oral hygiene status at individual, group, and population levels. We hypothesize that regular application of complex oral hygiene-prophylaxis could beneficially modulate salivary amino acids profile in children with different stage of plaque-induced gingivitis. Therefore, we aimed to study the salivary amino acids’ profile in relation to certain clinical indicators and environmental variables for plaque-induced gingivitis in children. Methods Fifty children (29 girls, 21 boys; mean age 8.18 ± 2.32 years) without anamnestic data for common diseases, no medication, and no data for allergy were selected. Plaque and gingival indexes were determined for assessment oral hygiene and plaque accumulation. Unstimulated whole saliva was collected, centrifuged and supernatants stored at −80 °C. Amino acid analysis was performed by liquid chromatography using analytical grade AccQ·Tag-Ultra-derivatization kit. Results Gingivitis was indicated in most of the examined children over 6 years. More than half (63.6 %) of them revealed moderate stage of the disease and a tendency to satisfactory good oral hygiene and degree of gingival inflammation. Salivary glycine, proline, arginine, serine, lysine, aspartate, glutamate, threonine, methionine, and isoleucine were higher in gingivitis children, while cysteine, tyrosine and phenylalanine decrease. In gingivitis children without regular oral hygiene-prophylaxis, some structural amino acids like glycine and proline were increased, while amino acids with protective antioxidant potential like cysteine were diminished. Conclusions Plaque-induced gingivitis is associated with increased salivary levels of certain amino acids. These may serve as distinguishing markers among children with gingivitis.
摘要目的菌斑性牙龈炎是儿童时期最广泛分布的牙周疾病之一。菌斑潜在致病性的控制与个人、群体和人群的口腔卫生状况有关。我们假设定期应用复杂的口腔卫生预防可以有益地调节不同阶段的牙菌斑性牙龈炎儿童的唾液氨基酸谱。因此,我们旨在研究儿童牙菌斑性牙龈炎的唾液氨基酸谱与某些临床指标和环境变量的关系。方法50例儿童(女孩29例,男孩21例;平均年龄(8.18±2.32 岁),无常见病记忆资料,无用药记录,无过敏记录。测定菌斑和牙龈指标,评估口腔卫生和菌斑积累情况。收集未受刺激的全唾液,离心,上清保存在- 80 °C。采用分析级AccQ·tag - ultra衍生化试剂盒,液相色谱法分析氨基酸。结果6岁以上儿童牙龈炎占绝大多数。超过一半(63.6% %)的患者表现为中等程度的疾病,口腔卫生和牙龈炎症程度较好。牙龈炎患儿唾液甘氨酸、脯氨酸、精氨酸、丝氨酸、赖氨酸、天冬氨酸、谷氨酸、苏氨酸、蛋氨酸、异亮氨酸升高,半胱氨酸、酪氨酸、苯丙氨酸降低。在未进行常规口腔卫生预防的牙龈炎患儿中,部分结构氨基酸如甘氨酸和脯氨酸增加,而具有保护性抗氧化潜力的氨基酸如半胱氨酸减少。结论:牙菌斑性牙龈炎与唾液中某些氨基酸水平升高有关。这些可以作为区分牙龈炎儿童的标志。
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引用次数: 0
Mean platelet volume, neutrophil/lymphocyte ratio, platelet/lymphocyte ratio and early post-operative anesthesia complications 平均血小板体积、中性粒细胞/淋巴细胞比值、血小板/淋巴细胞比值及术后早期麻醉并发症
Pub Date : 2023-08-08 DOI: 10.1515/tjb-2023-0040
A. Altınbaş, Azime Bulut
Abstract Objectives We aimed to establish the relationship between pre-operatively measured mean platelet volume (MPV), neutrophil/lymphocyte ratio (NLR), platelet/lymphocyte ratio (PLR) values and early anesthetic complications like bronchospasm & laryngospasm and hypotension in patients undergoing adenotonsillar surgery and non-adenotonsillar surgeries in both pediatric and adult population. Methods Patients from both sexes aged 1–63 years, and the American Society of Anesthesiology (ASA) physical status I–II were included in the study with elective adenotonsillectomy and non-adenotonsillar surgeries. Results In total, we included 330 patients in our study. The respiratory complications observed significantly more frequent in pediatric adenotonsillar surgery group (p=0.001). When the post-operative complications were compared with the MPV, NLR and PLR values, it was observed that the MPV values were significantly higher in patients who had hypotension (p=0.01) and PLR values were significantly higher in pediatric adenotonsillectomy group who developed bronchospasm and laryngospasm. There was no relationship between other complications and the laboratory values of the groups. Conclusions In the study, we found that PLR values were significantly high in the pediatric patients having hypoxia who underwent adenotonsillectomy. MPV values were significantly high in the patients who had hypotension in the early post-operative period. Based on these findings, it has been suggested that pre-operative PLR value can be a predicting guide for bronchospasm, laryngospasm. On the other hand, MPV values can be used as a guide in terms of predicting hypotension.
目的探讨儿童和成人腺扁桃体手术和非腺扁桃体手术患者术前平均血小板体积(MPV)、中性粒细胞/淋巴细胞比值(NLR)、血小板/淋巴细胞比值(PLR)值与支气管痉挛、喉痉挛、低血压等早期麻醉并发症的关系。方法选取年龄1 ~ 63岁 岁,身体状态为美国麻醉学学会(ASA) I-II级的患者,择期行腺扁桃体切除术和非腺扁桃体手术。结果共纳入330例患者。小儿腺扁桃体手术组呼吸系统并发症发生率显著高于对照组(p=0.001)。将术后并发症与MPV、NLR、PLR值进行比较,发现低血压组MPV值明显增高(p=0.01),小儿腺扁桃体切除术组出现支气管痉挛、喉痉挛的患者PLR值明显增高。其他并发症与两组实验值无关系。结论在本研究中,我们发现儿童缺氧患者行腺扁桃体切除术后PLR值明显较高。术后早期低血压患者的MPV值明显偏高。基于这些发现,建议术前PLR值可作为支气管痉挛、喉痉挛的预测指南。另一方面,MPV值可以作为预测低血压的指导。
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引用次数: 1
Predictive value of nesfatin-1 in heart failure mortality nesfatin-1对心力衰竭死亡率的预测价值
Pub Date : 2023-07-31 DOI: 10.1515/tjb-2022-0227
M. Kerkutluoglu, H. Gunes, Ali Eren Onus, M. Dagli, O. Yucel
Abstract Objectives Advanced heart failure is the last stage of heart failure in which the life expectancy of patients is significantly reduced. Many mortality markers have been identified in advanced heart failure. Although the nesfatin-1 molecule is known as a satiety hormone, it has also been shown to be associated with many cardiovascular diseases. This study aims to elucidate the association between in-hospital mortality and nesfatin-1 level in advanced heart failure patients. Methods The research included 74 cases of advanced heart failure. During the coronary intensive care surveillance of these patients, 22 patients had in-hospital mortality. The cases, divided into groups with and without in-hospital mortality, were compared using laboratory data, echocardiography, and demographic properties. Results The age of the cases with in-hospital mortality was older than the cases without mortality [(74 (66–95) vs. 67 (26–90); p=0.019)]. Serum nesfatin-1 level and tricuspid annular plane systolic excursion (TAPSE) were statistically lower in the in-hospital mortality group (43.8 ± 5.5 vs. 40.5 ± 6.1; p=0.027, 13.5 ± 1.9 vs. 16.2 ± 2.6 p=0.001, respectively). Serum nesfatin-1 level and TAPSE were detected as independent predictors for in-hospital mortality in advanced heart failure via multivariate analysis using parameters that were significant in the univariate analysis. Receiver operator characteristic curve analysis showed that the optimum cut-off level for Nesfatin-1 in determining in-hospital mortality was ≤23.57 (pg/mL) with a specificity of 73.1 % and a sensitivity of 77.3 % (AUC=0.763, 95 % CI=0.647–0.879, p<0.001). Conclusions This research revealed that in advanced heart failure patients, serum nesfatin-1 amounts are associated with mortality and seem to be an independent predictor of mortality.
摘要目的晚期心力衰竭是心力衰竭的最后阶段,患者的预期寿命明显降低。在晚期心力衰竭中已经发现了许多死亡标志。虽然nesfatin-1分子被认为是一种饱腹感激素,但它也被证明与许多心血管疾病有关。本研究旨在探讨晚期心力衰竭患者住院死亡率与nesfatin-1水平的关系。方法对74例晚期心力衰竭患者进行回顾性分析。在这些患者的冠状动脉重症监护监测期间,22例患者发生院内死亡。将这些病例分为有住院死亡率和无住院死亡率两组,使用实验室数据、超声心动图和人口统计学特征对其进行比较。结果院内死亡病例年龄大于无死亡病例[74(66 ~ 95)比67 (26 ~ 90)];p = 0.019)。住院死亡组血清nesfatin-1水平和三尖瓣环面收缩偏移(TAPSE)均较低(43.8±5.5∶40.5±6.1;P =0.027, 13.5±1.9 vs. 16.2±2.6 P =0.001)。血清nesfatin-1水平和TAPSE通过多变量分析检测为晚期心力衰竭住院死亡率的独立预测因子,使用单变量分析中显著的参数。受试者特征曲线分析显示,Nesfatin-1测定院内死亡率的最佳临界值≤23.57 (pg/mL),特异性为73.1 %,敏感性为77.3 % (AUC=0.763, 95 % CI= 0.647-0.879, p<0.001)。本研究表明,在晚期心力衰竭患者中,血清nesfatin-1含量与死亡率相关,似乎是死亡率的独立预测因子。
{"title":"Predictive value of nesfatin-1 in heart failure mortality","authors":"M. Kerkutluoglu, H. Gunes, Ali Eren Onus, M. Dagli, O. Yucel","doi":"10.1515/tjb-2022-0227","DOIUrl":"https://doi.org/10.1515/tjb-2022-0227","url":null,"abstract":"Abstract Objectives Advanced heart failure is the last stage of heart failure in which the life expectancy of patients is significantly reduced. Many mortality markers have been identified in advanced heart failure. Although the nesfatin-1 molecule is known as a satiety hormone, it has also been shown to be associated with many cardiovascular diseases. This study aims to elucidate the association between in-hospital mortality and nesfatin-1 level in advanced heart failure patients. Methods The research included 74 cases of advanced heart failure. During the coronary intensive care surveillance of these patients, 22 patients had in-hospital mortality. The cases, divided into groups with and without in-hospital mortality, were compared using laboratory data, echocardiography, and demographic properties. Results The age of the cases with in-hospital mortality was older than the cases without mortality [(74 (66–95) vs. 67 (26–90); p=0.019)]. Serum nesfatin-1 level and tricuspid annular plane systolic excursion (TAPSE) were statistically lower in the in-hospital mortality group (43.8 ± 5.5 vs. 40.5 ± 6.1; p=0.027, 13.5 ± 1.9 vs. 16.2 ± 2.6 p=0.001, respectively). Serum nesfatin-1 level and TAPSE were detected as independent predictors for in-hospital mortality in advanced heart failure via multivariate analysis using parameters that were significant in the univariate analysis. Receiver operator characteristic curve analysis showed that the optimum cut-off level for Nesfatin-1 in determining in-hospital mortality was ≤23.57 (pg/mL) with a specificity of 73.1 % and a sensitivity of 77.3 % (AUC=0.763, 95 % CI=0.647–0.879, p<0.001). Conclusions This research revealed that in advanced heart failure patients, serum nesfatin-1 amounts are associated with mortality and seem to be an independent predictor of mortality.","PeriodicalId":23344,"journal":{"name":"Turkish Journal of Biochemistry","volume":"7 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91334593","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of the monocyte-to-lymphocyte ratio (MLR) and c-reactive protein (CRP) as diagnostic biomarkers in different lung diseases, especially for SCLC 单核细胞与淋巴细胞比值(MLR)和c反应蛋白(CRP)作为不同肺部疾病,特别是SCLC的诊断生物标志物的评价
Pub Date : 2023-07-27 DOI: 10.1515/tjb-2022-0282
Yue Zhang, Zhigang Xin, Qun Zhang, Zhijun Zhang, Xiao-yuan Feng
Abstract Objectives This study aims to assess the capability of monocyte-to-lymphocyte ratio (MLR) and C-reactive protein (CRP) to diagnose and differentiate diagnosis various types of lung diseases, including non-small-cell lung cancer (NSCLC), small-cell lung cancer (SCLC) and benign pulmonary diseases (BPD). Methods Patients diagnosed with lung cancer and BPD by pathology and healthy volunteers were enrolled. Laboratory test data and clinical pathologic characteristics were recorded, including complete blood counts, CRP, NSE, CYFRA21-1 levels, age, gender, and histological type. The differences between the groups were calculated and compared. Receiver operating characteristic (ROC) analysis was performed to specify the diagnostic value of MLR and CRP in NSCLC, SCLC, and BPD. Results 2042 patients and 996 healthy volunteers were involved (NSCLC, SCLC, and BPD patients were 1,245, 302, and 495, respectively). Compared to healthy volunteers, MLR and CRP in patients with NSCLC, SCLC, and BPD were significantly higher (p<0.0001). The areas under the curve (AUC) were 0.703, 0.828, 0.784, 0.703, 0.813, and 0.798, respectively. Through the combined analysis of MLR and CRP, the AUC could be improved to 0.765, 0.882, and 0.843, respectively. Additionally, an evaluation of the diagnostic value of MLR+CRP+ NSE+CYFRA21-1 gave the AUC of 0.898 (95 % CI:0.882–0.914), 0.986 (95 % CI:0.975–0.996) and 0.925 (95 % CI:0.906–0.945), respectively. Moreover, MLR and CRP could differentiate early-stage patients (0 and I stages) from late-stage (IV stage) for NSCLC and SCLC patients, with p-values of less than 0.0001, respectively. Conclusions MLR and CRP could be good diagnostic indicators of lung diseases, especially for SCLC and BPD. Both could improve the diagnostic efficiency of traditional lung cancer biomarkers, demonstrating excellent diagnostic value, particularly in SCLC. This may supply early treatment and survival advantages for patients.
摘要目的探讨单核细胞与淋巴细胞比值(MLR)和c反应蛋白(CRP)对非小细胞肺癌(NSCLC)、小细胞肺癌(SCLC)和良性肺疾病(BPD)等多种肺部疾病的诊断和鉴别诊断能力。方法选择经病理诊断为肺癌和BPD的患者和健康志愿者。记录实验室检查资料和临床病理特征,包括全血细胞计数、CRP、NSE、CYFRA21-1水平、年龄、性别、组织学类型。计算并比较两组间的差异。采用受试者工作特征(ROC)分析,明确MLR和CRP在NSCLC、SCLC和BPD中的诊断价值。结果共纳入2042例患者和996名健康志愿者(NSCLC、SCLC和BPD患者分别为1245例、302例和495例)。与健康志愿者相比,NSCLC、SCLC和BPD患者的MLR和CRP显著升高(p<0.0001)。曲线下面积(AUC)分别为0.703、0.828、0.784、0.703、0.813和0.798。通过MLR和CRP的联合分析,AUC分别提高到0.765、0.882和0.843。此外,评估MLR+CRP+ NSE+CYFRA21-1的诊断价值,AUC分别为0.898(95 % CI: 0.882-0.914)、0.986(95 % CI: 0.975-0.996)和0.925(95 % CI: 0.906-0.945)。此外,MLR和CRP可以区分NSCLC和SCLC患者的早期(0期和I期)和晚期(IV期),p值分别小于0.0001。结论MLR和CRP可作为肺部疾病的良好诊断指标,尤其对SCLC和BPD有较好的诊断价值。两者均能提高传统肺癌生物标志物的诊断效率,表现出优异的诊断价值,尤其是对SCLC的诊断价值。这可能为患者提供早期治疗和生存优势。
{"title":"Evaluation of the monocyte-to-lymphocyte ratio (MLR) and c-reactive protein (CRP) as diagnostic biomarkers in different lung diseases, especially for SCLC","authors":"Yue Zhang, Zhigang Xin, Qun Zhang, Zhijun Zhang, Xiao-yuan Feng","doi":"10.1515/tjb-2022-0282","DOIUrl":"https://doi.org/10.1515/tjb-2022-0282","url":null,"abstract":"Abstract Objectives This study aims to assess the capability of monocyte-to-lymphocyte ratio (MLR) and C-reactive protein (CRP) to diagnose and differentiate diagnosis various types of lung diseases, including non-small-cell lung cancer (NSCLC), small-cell lung cancer (SCLC) and benign pulmonary diseases (BPD). Methods Patients diagnosed with lung cancer and BPD by pathology and healthy volunteers were enrolled. Laboratory test data and clinical pathologic characteristics were recorded, including complete blood counts, CRP, NSE, CYFRA21-1 levels, age, gender, and histological type. The differences between the groups were calculated and compared. Receiver operating characteristic (ROC) analysis was performed to specify the diagnostic value of MLR and CRP in NSCLC, SCLC, and BPD. Results 2042 patients and 996 healthy volunteers were involved (NSCLC, SCLC, and BPD patients were 1,245, 302, and 495, respectively). Compared to healthy volunteers, MLR and CRP in patients with NSCLC, SCLC, and BPD were significantly higher (p<0.0001). The areas under the curve (AUC) were 0.703, 0.828, 0.784, 0.703, 0.813, and 0.798, respectively. Through the combined analysis of MLR and CRP, the AUC could be improved to 0.765, 0.882, and 0.843, respectively. Additionally, an evaluation of the diagnostic value of MLR+CRP+ NSE+CYFRA21-1 gave the AUC of 0.898 (95 % CI:0.882–0.914), 0.986 (95 % CI:0.975–0.996) and 0.925 (95 % CI:0.906–0.945), respectively. Moreover, MLR and CRP could differentiate early-stage patients (0 and I stages) from late-stage (IV stage) for NSCLC and SCLC patients, with p-values of less than 0.0001, respectively. Conclusions MLR and CRP could be good diagnostic indicators of lung diseases, especially for SCLC and BPD. Both could improve the diagnostic efficiency of traditional lung cancer biomarkers, demonstrating excellent diagnostic value, particularly in SCLC. This may supply early treatment and survival advantages for patients.","PeriodicalId":23344,"journal":{"name":"Turkish Journal of Biochemistry","volume":"48 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84082037","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of concomitant leukemoid reaction and mucormycosis in a patient with severe COVID-19 infection 重症COVID-19感染伴白血病反应和毛霉菌病1例
Pub Date : 2023-07-27 DOI: 10.1515/tjb-2023-0016
Rand Sayed Issa, Gohar Mushtaq, A. Unnisa, A. Mahli
Abstract Objectives Leukemoid Reaction (LR) signifies leukocytosis characterized by mature neutrophils. The incidence of LR is about 1 % among hospitalized patients. Mucormycosis is a rare, aggressive, fatal fungal infection that afflicts immune-compromised patients. This study discusses the case of concomitant leukemoid reaction and mucormycosis in a patient with severe COVID-19 infection. Case presentation A 45-year-old female patient was presented to the hospital with confirmed SARS-CoV-2 and was given supplemental oxygen and placed on mechanical ventilation. Her skin biopsy revealed non-septate hyphae with wide-angle branching. Her blood tests also revealed the presence of LR. Conclusions Severe COVID-19 infection causes new-onset hyperglycemia, which can lead to metabolic acidosis, toxic metabolite accumulation in the body due to renal failure, the release of stress hormones and inflammatory cytokines, and the occurrence of secondary bacterial and opportunistic fungal infections. The study has shown that LR in severe COVID-19 may be associated with severe infections (bacterial or fungal) and other pathophysiological changes in the body.
目的白血病样反应(Leukemoid Reaction, LR)是指以成熟中性粒细胞为特征的白细胞增生。住院患者中LR的发生率约为1 %。毛霉病是一种罕见的,侵袭性的,致命的真菌感染,折磨免疫功能低下的患者。本研究讨论了一例重症COVID-19感染患者合并白血病反应和毛霉菌病的病例。一名确诊为SARS-CoV-2的45岁女性患者被送往医院,给予补充氧气并给予机械通气。她的皮肤活检显示无分隔菌丝和广角分支。她的血液检查也显示了LR的存在。结论重症COVID-19感染可引起新发高血糖,导致代谢性酸中毒,肾功能衰竭导致体内有毒代谢物积累,应激激素和炎症细胞因子释放,继发细菌和机会真菌感染。研究表明,严重COVID-19中的LR可能与严重感染(细菌或真菌)和体内其他病理生理变化有关。
{"title":"A case of concomitant leukemoid reaction and mucormycosis in a patient with severe COVID-19 infection","authors":"Rand Sayed Issa, Gohar Mushtaq, A. Unnisa, A. Mahli","doi":"10.1515/tjb-2023-0016","DOIUrl":"https://doi.org/10.1515/tjb-2023-0016","url":null,"abstract":"Abstract Objectives Leukemoid Reaction (LR) signifies leukocytosis characterized by mature neutrophils. The incidence of LR is about 1 % among hospitalized patients. Mucormycosis is a rare, aggressive, fatal fungal infection that afflicts immune-compromised patients. This study discusses the case of concomitant leukemoid reaction and mucormycosis in a patient with severe COVID-19 infection. Case presentation A 45-year-old female patient was presented to the hospital with confirmed SARS-CoV-2 and was given supplemental oxygen and placed on mechanical ventilation. Her skin biopsy revealed non-septate hyphae with wide-angle branching. Her blood tests also revealed the presence of LR. Conclusions Severe COVID-19 infection causes new-onset hyperglycemia, which can lead to metabolic acidosis, toxic metabolite accumulation in the body due to renal failure, the release of stress hormones and inflammatory cytokines, and the occurrence of secondary bacterial and opportunistic fungal infections. The study has shown that LR in severe COVID-19 may be associated with severe infections (bacterial or fungal) and other pathophysiological changes in the body.","PeriodicalId":23344,"journal":{"name":"Turkish Journal of Biochemistry","volume":"214 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75588254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Inhibitory effect of organic acids on human neutrophil Myeloperoxidase’s peroxidation, chlorination, and nitration activities 有机酸对人中性粒细胞髓过氧化物酶过氧化、氯化和硝化活性的抑制作用
Pub Date : 2023-07-21 DOI: 10.1515/tjb-2022-0260
B. Sarkarati
Abstract Objectives Myeloperoxidase from polymorphonuclear leukocytes is an important enzyme in oxidative metabolism and has a key role in tissue injuries in oxidative stress and inflammatory conditions. Therefore, its inhibitors have become the focus of studies on new drug development in recent years. The aim of the study was to determine the inhibitory effect of organic acids on the peroxidation, chlorination, and nitration activities of myeloperoxidase. Methods Seven organic acids naturally abundant in plants were tested. Different activities of myeloperoxidase were measured in the presence of various amounts of organic acids, and inhibition rates and kinetic parameters were determined for each organic acid separately. Results All the organic acids examined had inhibitory effects on the different activities of myeloperoxidase. Comparison of the IC50 values obtained for peroxidation, chlorination, and nitration activities showed that oxalic acid was the strongest inhibitor of myeloperoxidase activity, while citric acid and succinic acid were the weakest. Conclusions The results suggested that all the organic acids examined are inhibitors of myeloperoxidase. In particular, oxalic acid and fumaric acid are popular candidates for drug development research. More studies are needed to determine the in vivo effects of organic acids and their effects in the treatment of disease.
多形核白细胞髓过氧化物酶是一种重要的氧化代谢酶,在氧化应激和炎症条件下的组织损伤中起关键作用。因此,其抑制剂成为近年来新药开发的研究热点。本研究的目的是确定有机酸对髓过氧化物酶的过氧化、氯化和硝化活性的抑制作用。方法对植物中富含的7种天然有机酸进行测定。测定了不同有机酸对骨髓过氧化物酶活性的影响,并测定了不同有机酸对骨髓过氧化物酶的抑制率和动力学参数。结果所有有机酸均对脊髓过氧化物酶的不同活性有抑制作用。过氧化、氯化和硝化活性的IC50值比较表明,草酸是髓过氧化物酶活性最强的抑制剂,而柠檬酸和琥珀酸是最弱的抑制剂。结论所检测的有机酸均为髓过氧化物酶抑制剂。特别是草酸和富马酸是药物开发研究的热门候选物质。需要更多的研究来确定有机酸在体内的作用及其在疾病治疗中的作用。
{"title":"Inhibitory effect of organic acids on human neutrophil Myeloperoxidase’s peroxidation, chlorination, and nitration activities","authors":"B. Sarkarati","doi":"10.1515/tjb-2022-0260","DOIUrl":"https://doi.org/10.1515/tjb-2022-0260","url":null,"abstract":"Abstract Objectives Myeloperoxidase from polymorphonuclear leukocytes is an important enzyme in oxidative metabolism and has a key role in tissue injuries in oxidative stress and inflammatory conditions. Therefore, its inhibitors have become the focus of studies on new drug development in recent years. The aim of the study was to determine the inhibitory effect of organic acids on the peroxidation, chlorination, and nitration activities of myeloperoxidase. Methods Seven organic acids naturally abundant in plants were tested. Different activities of myeloperoxidase were measured in the presence of various amounts of organic acids, and inhibition rates and kinetic parameters were determined for each organic acid separately. Results All the organic acids examined had inhibitory effects on the different activities of myeloperoxidase. Comparison of the IC50 values obtained for peroxidation, chlorination, and nitration activities showed that oxalic acid was the strongest inhibitor of myeloperoxidase activity, while citric acid and succinic acid were the weakest. Conclusions The results suggested that all the organic acids examined are inhibitors of myeloperoxidase. In particular, oxalic acid and fumaric acid are popular candidates for drug development research. More studies are needed to determine the in vivo effects of organic acids and their effects in the treatment of disease.","PeriodicalId":23344,"journal":{"name":"Turkish Journal of Biochemistry","volume":"21 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84254450","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Quercetin induces cytotoxicity and apoptosis, reduces metastasis and drug resistance in oral cancer cells 槲皮素诱导口腔癌细胞毒性和凋亡,降低转移和耐药
Pub Date : 2023-07-20 DOI: 10.1515/tjb-2023-0003
Nan Li, Jun Wang
Abstract Quercetin is a plant flavonol from the flavonoid group of polyphenols or can also be formulated as a synthetic supplement chemically. Approximately 80 % of people in Africa and other developing nations still depend on traditional herbal remedies to treat ailments. Quercetin has been demonstrated to have a variety of anticancer effects. However, the effect of quercetin on oral cancer cells remains rare. According to our systematic review, quercetin includes anti-cell viability, anti-cell survival and anti-cell proliferation. Quercetin also possesses an anti-metastatic effect by regulating the expression of epithelial-to-mesenchymal transition-related genes in oral cancer cells. The apoptotic effect of quercetin in oral cancer cells is probably via inducing cell surface death receptors, endoplasmic reticulum stress and mitochondria-mediated signaling pathways. Additionally, quercetin reduces drug resistance in KB/vincristine oral cancer cells and enhances cell sensitivity to vincristine treatment. Quercetin induces apoptosis of human oral cancer SAS cells through the endoplasmic reticulum and mitochondria-mediated signaling pathways. Quercetin inhibits cell survival and metastatic ability via the epithelial-to-mesenchymal transition-mediated signaling pathways in oral squamous cell carcinoma. Quercetin is an anti-tumour agent candidate and can also inhibit oral tumour metastasis. Indeed, the efficacy of quercetin against chemically induced oral squamous cell carcinoma remains to be elucidated.
槲皮素是植物多酚类黄酮类化合物中的一种黄酮醇,也可以通过化学合成的方式进行补充。在非洲和其他发展中国家,大约80%的人仍然依靠传统的草药治疗疾病。槲皮素已被证明具有多种抗癌作用。然而,槲皮素对口腔癌细胞的作用仍然很少。根据系统综述,槲皮素包括抗细胞活力、抗细胞存活和抗细胞增殖。槲皮素还通过调节口腔癌细胞上皮向间质过渡相关基因的表达而具有抗转移作用。槲皮素对口腔癌细胞的凋亡作用可能是通过诱导细胞表面死亡受体、内质网应激和线粒体介导的信号通路实现的。此外,槲皮素可以降低KB/长春新碱口腔癌细胞的耐药性,并增强细胞对长春新碱治疗的敏感性。槲皮素通过内质网和线粒体介导的信号通路诱导人口腔癌SAS细胞凋亡。槲皮素通过上皮-间质过渡介导的信号通路抑制口腔鳞状细胞癌的细胞存活和转移能力。槲皮素是一种抗肿瘤的候选药物,也可以抑制口腔肿瘤的转移。事实上,槲皮素对化学诱导的口腔鳞状细胞癌的疗效仍有待阐明。
{"title":"Quercetin induces cytotoxicity and apoptosis, reduces metastasis and drug resistance in oral cancer cells","authors":"Nan Li, Jun Wang","doi":"10.1515/tjb-2023-0003","DOIUrl":"https://doi.org/10.1515/tjb-2023-0003","url":null,"abstract":"Abstract Quercetin is a plant flavonol from the flavonoid group of polyphenols or can also be formulated as a synthetic supplement chemically. Approximately 80 % of people in Africa and other developing nations still depend on traditional herbal remedies to treat ailments. Quercetin has been demonstrated to have a variety of anticancer effects. However, the effect of quercetin on oral cancer cells remains rare. According to our systematic review, quercetin includes anti-cell viability, anti-cell survival and anti-cell proliferation. Quercetin also possesses an anti-metastatic effect by regulating the expression of epithelial-to-mesenchymal transition-related genes in oral cancer cells. The apoptotic effect of quercetin in oral cancer cells is probably via inducing cell surface death receptors, endoplasmic reticulum stress and mitochondria-mediated signaling pathways. Additionally, quercetin reduces drug resistance in KB/vincristine oral cancer cells and enhances cell sensitivity to vincristine treatment. Quercetin induces apoptosis of human oral cancer SAS cells through the endoplasmic reticulum and mitochondria-mediated signaling pathways. Quercetin inhibits cell survival and metastatic ability via the epithelial-to-mesenchymal transition-mediated signaling pathways in oral squamous cell carcinoma. Quercetin is an anti-tumour agent candidate and can also inhibit oral tumour metastasis. Indeed, the efficacy of quercetin against chemically induced oral squamous cell carcinoma remains to be elucidated.","PeriodicalId":23344,"journal":{"name":"Turkish Journal of Biochemistry","volume":"3 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89261767","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Histone proteomics implicates H3K36me2 and its regulators in mouse embryonic stem cell pluripotency exit and lineage choice 组蛋白组学揭示了H3K36me2及其调控因子在小鼠胚胎干细胞多能性退出和谱系选择中的作用
Pub Date : 2023-07-19 DOI: 10.1515/tjb-2023-0030
Dersu Sezginmert, Nihal Terzİ ÇİzmecİoĞlu
Abstract Objectives Gene expression changes during embryonic stem cell (ESC) differentiation is regulated by epigenetic mechanisms. Understanding these can help uncover how cell fate decisions are made during early embryonic development. Comparison of chromatin of ESCs with lineage-committed cells can implicate chromatin factors functional in exit from pluripotency and the choice of proper lineages. Therefore, we quantitatively analyzed histone modifications in mouse ESC differentiation towards neuroectoderm and endoderm. Methods We cultured mouse ESCs (mESCs) and differentiated them towards neuroectoderm or endoderm lineages and performed mass spectrometry on total histones. Subsequent Western blots verified significantly altered H3K36me2. RT-qPCR analyses showed changes in H3K36-specific methyltransferases, demethylases and readers at mESC stage or during neuroectoderm/endoderm commitment. Results We presented quantitative histone modification levels in mESCs and lineage-committed cells. H3K36me2 increased specifically in neuroectoderm compared to mESCs or endoderm-committed cells. Regulation of H3K36 methylation might have a role in pluripotency exit and/or differentiation. Nsd2, Dnmt3b and Zmynd11 increased during differentiation regardless of lineage. Conversely, mESCs had higher Kdm4c and Msh6 expression than differentiated cells. Comparing neuroectoderm and endoderm-committed cells, we revealed Nsd1, Setd5 and Dnmt3a had lineage specific expression pattern. Conclusions Our results show quantitative changes in histone modifications during mESC lineage commitment and implicate H3K36me2 regulation for not only pluripotency exit but also lineage choice. Its regulatory proteins show stage (mESC vs. committed) or lineage (neuroectoderm vs. endoderm) dependent expression changes. Further work will be needed to discover their possible involvement in cell fate decisions and target genes.
【摘要】目的胚胎干细胞(ESC)分化过程中基因表达变化受表观遗传机制调控。了解这些可以帮助揭示细胞命运是如何在早期胚胎发育过程中决定的。比较ESCs与谱系承诺细胞的染色质可以暗示染色质因子在多能性退出和适当谱系选择中的功能。因此,我们定量分析了小鼠ESC向神经外胚层和内胚层分化过程中的组蛋白修饰。方法培养小鼠ESCs,将其分化为神经外胚层和内胚层谱系,并对总组蛋白进行质谱分析。随后的Western blots证实H3K36me2显著改变。RT-qPCR分析显示,在mESC阶段或神经外胚层/内胚层发育期间,h3k36特异性甲基转移酶、去甲基化酶和读取器发生了变化。结果我们在mESCs和谱系承诺细胞中获得了定量的组蛋白修饰水平。与mESCs或内胚层细胞相比,H3K36me2在神经外胚层中特异性增加。H3K36甲基化的调控可能在多能性退出和/或分化中起作用。无论谱系如何,Nsd2、Dnmt3b和Zmynd11在分化过程中均有所增加。相反,mESCs的Kdm4c和Msh6表达高于分化后的细胞。比较神经外胚层细胞和内胚层细胞,我们发现Nsd1、Setd5和Dnmt3a具有谱系特异性表达模式。我们的研究结果表明,组蛋白修饰在mESC谱系承诺过程中发生了定量变化,并暗示H3K36me2调控不仅影响多能性退出,还影响谱系选择。其调节蛋白表现出阶段(mESC vs. committed)或谱系(神经外胚层vs.内胚层)依赖性表达变化。需要进一步的工作来发现它们可能参与细胞命运决定和靶基因。
{"title":"Histone proteomics implicates H3K36me2 and its regulators in mouse embryonic stem cell pluripotency exit and lineage choice","authors":"Dersu Sezginmert, Nihal Terzİ ÇİzmecİoĞlu","doi":"10.1515/tjb-2023-0030","DOIUrl":"https://doi.org/10.1515/tjb-2023-0030","url":null,"abstract":"Abstract Objectives Gene expression changes during embryonic stem cell (ESC) differentiation is regulated by epigenetic mechanisms. Understanding these can help uncover how cell fate decisions are made during early embryonic development. Comparison of chromatin of ESCs with lineage-committed cells can implicate chromatin factors functional in exit from pluripotency and the choice of proper lineages. Therefore, we quantitatively analyzed histone modifications in mouse ESC differentiation towards neuroectoderm and endoderm. Methods We cultured mouse ESCs (mESCs) and differentiated them towards neuroectoderm or endoderm lineages and performed mass spectrometry on total histones. Subsequent Western blots verified significantly altered H3K36me2. RT-qPCR analyses showed changes in H3K36-specific methyltransferases, demethylases and readers at mESC stage or during neuroectoderm/endoderm commitment. Results We presented quantitative histone modification levels in mESCs and lineage-committed cells. H3K36me2 increased specifically in neuroectoderm compared to mESCs or endoderm-committed cells. Regulation of H3K36 methylation might have a role in pluripotency exit and/or differentiation. Nsd2, Dnmt3b and Zmynd11 increased during differentiation regardless of lineage. Conversely, mESCs had higher Kdm4c and Msh6 expression than differentiated cells. Comparing neuroectoderm and endoderm-committed cells, we revealed Nsd1, Setd5 and Dnmt3a had lineage specific expression pattern. Conclusions Our results show quantitative changes in histone modifications during mESC lineage commitment and implicate H3K36me2 regulation for not only pluripotency exit but also lineage choice. Its regulatory proteins show stage (mESC vs. committed) or lineage (neuroectoderm vs. endoderm) dependent expression changes. Further work will be needed to discover their possible involvement in cell fate decisions and target genes.","PeriodicalId":23344,"journal":{"name":"Turkish Journal of Biochemistry","volume":"37 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86611379","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Turkish Journal of Biochemistry
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