Diagnostic and prognostic value of circular RNA CDR1as/ciRS‐7 for solid tumours: A systematic review and meta‐analysis

The circular RNA, CDR1as/ciRS‐7, functions as a vital regulator in various cancers; however, the predictive value of CDR1as remains controversial. Therefore, a comprehensive analysis for clarifying the precise diagnostic and prognostic value of CDR1as in solid tumours is needed. A literature review of several databases was conducted for identifying potential studies. Pooled odds ratios (ORs) and hazard ratios (HRs) were used for evaluating the diagnostic accuracy variables and survival. Overall, 15 studies (1787 patients) and 11 studies (1578 patients) were included for diagnostic and prognostic outcome syntheses, respectively. Up‐regulated CDR1as expression was found to be correlated with worse clinicopathological characteristics, including the T status, N status, histological grade, TNM stage and distant metastasis. The synthesized sensitivity was 0.72 (95% confidence interval [CI], 0.65‐0.79), and the specificity was 0.80 (95% CI, 0.74‐0.86). The positive likelihood ratio (LR), negative LR and diagnostic odds ratio (DOR) were 3.70, 0.34 and 10.80, respectively. The area under the receiver operator characteristic curve was 0.84 (95% CI, 0.80‐0.87). In the pooled prognostic analysis, patients with high CDR1as expression had worse overall survival (HR = 2.40, P < 0.001) and disease‐free survival (HR = 1.74, P < 0.001). These results suggest that CDR1as is a reliable diagnostic and prognostic biomarker with high accuracy and efficiency, which may potentially facilitate clinical decisions on solid tumours in the future.     

用染料修饰吐温80液—固萃取体系从猪心肌匀浆液中分离纯化心肌黄酶

用三嗪类染料 Ｃｉｂａｃｒｏｎ Ｂｌｕｅ Ｆ３Ｇ－Ａ修饰的吐温８０,与吐温８０、硫酸被构成液－固萃取体系,从猪心肌匀浆液中分离纯化心肌黄酶。研究了吐温８０染料修饰物在吐温８０相中所占的比例、分相盐浓度、溶液的酸度、匀浆液的加入量等对匀浆液中酶及杂蛋白在两相中分配的影响。在室温条件下,酶选择性地进入吐温８０固相,杂蛋白主要留在盐水相。匀浆液中心肌黄酶的酶活力平均收得率为８１．４％,一步纯化倍数为６．６。降低盐浓度,提高盐水相酸度,能使酶从吐温８０固相反萃到盐水相。     

Serum Macroelement and Microelement Concentrations in Patients with Polycystic Ovary Syndrome: a Cross-Sectional Study

Polycystic ovarian syndrome (PCOS) is one of the most common endocrine diseases. However, its pathogenesis is unclear. We aim to explore the potential relationships between serum macroelements/microelements and PCOS. A total of 1137 women were involved in the current study. PCOS was defined according to ESHRE/ASRM, and complete blood samples were collected. Serum macroelements (calcium and magnesium) and microelements (copper, zinc, and iron) were assayed through atomic absorption spectrophotometry. PCOS patients had significantly higher copper concentrations than patients without PCOS (P < 0.001). By contrast, PCOS patients had lower serum calcium levels than patients without PCOS (P < 0.001). No significant differences were observed in the levels of serum zinc, magnesium, and iron between PCOS and non-PCOS patients. PCOS patients with acne had higher magnesium levels than those without acne (P = 0.020), and PCOS patients with hirsutism had lower magnesium levels than those without hirsutism (P = 0.037). High serum copper and low calcium levels may be correlated with PCOS. Magnesium concentrations are correlated with acne and hirsutism in PCOS patients. These results provide clues to explore the mechanism of PCOS and guidance for element treatments in PCOS patients.     

阿霉素铁(Ⅲ)配合物与DNA结合作用的研究

应用吸收光谱法研究了阿霉素铁（Ⅲ）［ＡＤＭ·Ｆｅ（Ⅲ）］与ＤＮＡ的结合作用,结果表明ＡＤＭ·Ｆｅ（Ⅲ）作为一个整体嵌入ＤＮＡ碱基之间形成ＡＤＭ·Ｆｅ（Ⅲ）·ＤＮＡ三元复合物。应用荧光淬灭法得到了不同Ｎａ＋浓度下ＡＤＭ及ＡＤＭ·Ｆｅ（Ⅲ）与ＤＮＡ结合作用的结合常数（Ｋ）、结合位点距离（ｎ）及标准自由能（ΔＧ）,并根据多聚电解质理论将ΔＧ分解为电荷作用部分（ΔＧｐｅ）及非电荷作用部分（ΔＧｔ）。结果表明ＡＤＭ·Ｆｅ（Ⅲ）中铁离子直接参与了与ＤＮＡ的作用,ＡＤＭ·Ｆｅ（Ⅲ）较ＡＤＭ更易与ＤＮＡ结合,且结合更为紧密     

短序与阔叶十大功劳化学组分及小檗碱含量的FTIR比较研究

为快速评价短序与阔叶十大功劳不同部位化学成分差异,本研究运用FTIR采集短序和阔叶十大功劳不同部位的红外光谱并比较短序与阔叶十大功劳不同部位盐酸小檗碱含量差异.研究结果显示,生物碱、黄酮和丁香酯等化学成分,短序十大功劳根、茎及叶片中均较阔叶十大功劳丰富,但是,多糖和苷类含量在两种十大功劳根中相当,在茎和叶片中均以阔叶十大功劳含量高,尤其是叶片中这种差异更明显.最后,与盐酸小檗碱标准品比较发现,2种十大功劳中盐酸小檗碱含量均以茎中最高,叶片中含量最低;2种十大功劳比较各部位盐酸小檗碱含量均以短序十大功劳中高.故运用FTIR技术可以快速找出2种十大功劳化学成分的差异,本研究结果将为十大功劳属植物资源合理开发利用及良种选育提供参考.     

Discovery of 5-(arenethynyl) hetero-monocyclic derivatives as potent inhibitors of BCR-ABL including the T315I gatekeeper mutant

Ponatinib (AP24534) was previously identified as a pan-BCR-ABL inhibitor that potently inhibits the T315I gatekeeper mutant, and has advanced into clinical development for the treatment of refractory or resistant CML. In this study, we explored a novel series of five and six membered monocycles as alternate hinge-binding templates to replace the 6,5-fused imidazopyridazine core of ponatinib. Like ponatinib, these monocycles are tethered to pendant toluanilides via an ethynyl linker. Several compounds in this series displayed excellent in vitro potency against both native BCR-ABL and the T315I mutant. Notably, a subset of inhibitors exhibited desirable PK and were orally active in a mouse model of T315I-driven CML.     

A systematic review of metabolomics biomarkers for Bisphenol A exposure

Introduction

Bisphenol A (BPA), 2,2-bis(4-hydroxyphenyl) propane, a common industrial chemical which has extremely huge production worldwide, is ubiquitous in the environment. Human have high risk of exposing to BPA and the health problems caused by BPA exposure have aroused public concern. However, the biomarkers for BPA exposure are lacking. As a rapidly developing subject, metabolomics has accumulated a large amount of valuable data in various fields. The secondary application of published metabolomics data could be a very promising field for generating novel biomarkers whilst further understanding of toxicity mechanisms.

Objectives

To summarize the published literature on the use of metabolomics as a tool to study BPA exposure and provide a systematic perspectives of current research on biomarkers screening of BPA exposure.

Methods

We conducted a systematic search of MEDLINE (PubMed) up to the end of June 25, 2017 with the key term combinations of ‘metabolomics’, ‘metabonomics’, ‘mass spectrometry’, ‘nuclear magnetic spectroscopy’, ‘metabolic profiling’ and ‘amino acid profile’ combined with ‘BPA exposure’. Additional articles were identified through searching the reference lists from included studies.

Results

This systematic review included 15 articles. Intermediates of glycolysis, Krebs cycle, β oxidation of long chain fatty acids, pentose phosphate pathway, nucleoside metabolism, branched chain amino acid metabolism, aromatic amino acids metabolism, sulfur-containing amino acids metabolism were significantly changed after BPA exposure, suggesting BPA had a highly complex toxic effects on organism which was consistent with existing studies. The biomarkers most consistently associated with BPA exposure were lactate and choline.

Conclusion

Existing metabolomics studies of BPA exposure present heterogeneous findings regarding metabolite profile characteristics. We need more evidence from target metabolomics and epidemiological studies to further examine the reliability of these biomarkers which link to low, environmentally relevant, exposure of BPA in human body.

     

Role of Complement 3 in TNF-α-Induced Mesenchymal Transition of Renal Tubular Epithelial Cells In Vitro

Injured renal tubular epithelial cells (RTECs) have been recently thought to directly contribute to the accumulation of myofibroblasts in renal tubulointerstitial fibrosis through a process of epithelial to mesenchymal transition (EMT). However, the factors inducing RTECs to undergo EMT and the underlying mechanisms need to be further elucidated. This study aimed to determine the EMT-inducing activity of proinflammatory cytokine TNF-α and the role for complement 3 (C3) in this activity in an in vitro model of human RTECs (HK-2 cells). Wild type HK-2 cells were treated with TNF-α, IFN-γ or C3a; C3 siRNA- or control siRNA-carrying HK-2 cells were treated with TNF-α. Changes in the cell morphology and phenotype were assessed by microscopy, RT-PCR, western blotting, and immunostaining. TNF-α effectively induced HK-2 cells to express C3 and to transform into morphologically myofibroblast-like cells that lost E-cadherin (a classical epithelial cell marker) expression but acquired alpha-smooth muscle actin (α-SMA, a classical myofibroblast differentiation marker) expression. C3 siRNA robustly attenuated all the morphologic and phenotypic changes induced by TNF-α but the control siRNA showed no effect. Our preliminary observations suggest that TNF-α may induce EMT in RTECs through inducing C3 expression.