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Statement of Retraction: The abnormal expression of chromosomal region maintenance 1 (CRM1)-survivin axis in ovarian cancer and its related mechanisms regulating proliferation and apoptosis of ovarian cancer cells. 撤回声明:染色体区域维护1(CRM1)-生存素轴在卵巢癌中的异常表达及其调控卵巢癌细胞增殖和凋亡的相关机制
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299572
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引用次数: 0
Enzymatic synthesis of Hydroxytyrosol from Oleuropein for valorization of an agricultural waste. 通过酶法合成油菜素中的羟基酪醇,实现农业废弃物的价值化。
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2024-09-05 DOI: 10.1080/21655979.2024.2396647
Gabriel García-Molina, Eduard Peters, Rosa Palmeri, Yaregal Awoke, Carlos Márquez-Álvarez, Rosa M Blanco

Oleuropein (OP) is an appreciated compound present not only in fruits but also in leaves of olive trees, which can be transformed into hydroxytyrosol (HT), a substance with high antioxidant activity. In this work, the transformation of an agricultural residue containing OP (olive leaves or wastewater from mills) to the high added value compound HT is accomplished through different enzymatic strategies. Different enzymes were used, immobilized on various supports by diverse binding forces: beta-glucosidase encapsulated in siliceous material, esterases and lipases immobilized on hydrophobic supports (octyl-functionalized amorphous silica and periodic mesoporous organosilica), and esterase immobilized on amine-functionalized ordered mesoporous silica. All these biocatalysts were tested for oleuropein hydrolysis through two different reaction approaches: a) split of glucosidic bond catalyzed by beta-glucosidase (β-glu), followed by hydrolysis of the aglycon and further ester hydrolysis. 5 mg·mL-1 of β-glu fully hydrolyzed 5 mM OP at pH 7 and 50°C in 7 days, and further enzymatic hydrolysis of the aglycon yielded near to 0.5 mM HT in the best conditions tested. b) via direct hydrolysis of the ester bond to produce hydroxytyrosol in a one-step reaction using esterases or lipases. The latter reaction pathway catalyzed by lipase from Penicillium camemberti immobilized on octyl-silica (4 mg·mL-1) at 35°C and pH 6 directly produced 6.8 mM HT (1 mg·mL-1), transforming in 12 days near to 30% of the initial 25 mM OP from a commercial olive leaves extract.

橄榄油素(OP)是一种值得赞赏的化合物,不仅存在于橄榄果实中,也存在于橄榄树叶中,它可以转化为羟基酪醇(HT),一种具有高抗氧化活性的物质。在这项工作中,通过不同的酶解策略,将含有 OP 的农业残留物(橄榄叶或工厂废水)转化为高附加值化合物 HT。使用了不同的酶,通过不同的结合力固定在不同的支撑物上:硅质材料中封装的β-葡萄糖苷酶、固定在疏水性支撑物(辛基功能化无定形二氧化硅和周期性介孔有机硅)上的酯酶和脂肪酶,以及固定在胺功能化有序介孔二氧化硅上的酯酶。所有这些生物催化剂都通过两种不同的反应方法进行了油菜素水解测试:a)β-葡萄糖苷酶(β-glu)催化的葡萄糖苷键分裂,然后水解苷元并进一步水解酯。在 pH 值为 7、温度为 50°C 的条件下,5 毫克/毫升-1 的 β-glu 可在 7 天内完全水解 5 毫摩尔的 OP,在测试的最佳条件下,苷元的进一步酶水解可产生接近 0.5 毫摩尔的 HT。 b) 使用酯酶或脂肪酶通过一步反应直接水解酯键产生羟基酪醇。在 35°C 和 pH 值为 6 的条件下,固定在辛基二氧化硅(4 毫克/毫升-1)上的卡门贝青霉菌脂肪酶催化的后一种反应途径可直接产生 6.8 毫摩尔 HT(1 毫克/毫升-1),并在 12 天内将商业橄榄叶提取物中 25 毫摩尔 OP 的 30% 转化为羟基酪醇。
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引用次数: 0
miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2. miR-148-3p 通过靶向 Bcl2 抑制胃癌细胞的恶性表型和化疗耐药性。
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2021-11-16 DOI: 10.1080/21655979.2021.2005742
Hongyan Zhang, Feng Liang, Fei Wang, Qianru Xu, Yuxuan Qiu, Xin Lu, Lin Jiang, Kaiyu Jian

Gastric cancer (GC) is the fourth most common cancer in the world. This work was designed to explore the biological effects of miR-148-3p on GC. Quantitative reverse transcription-polymerase chain reaction (RT-qPCR) was utilized to analyze the mRNA expression of miR-148-3p in GC cell lines. The mimics and inhibitors of miR-148-3p were carefully transfected into GC cells to up-regulate or down-regulate miR-148-3p expression. Observe the effect on miR-148-3p expression change to GC cell proliferation, colony formation, tumorigenesis, chemotherapy sensitivity, transwell migration, and invasion. Use online database tool to predict the miR-148-3p promising targets, and can be verified via RT-qPCR, Western blot, and luciferase report. We found that miR-148-3p expression level in GC cells was markedly down-regulated (P < 0.05), as compared with human normal gastric mucosal cells GES-1. Otherwise, miR-148-3p overexpression could effectively inhibit the cell proliferation, cell cycle progress, colony formation, anti-apoptosis, anti-migration and anti-invasion in gastric cancer cells, whereas miR-148-3p inhibition exhibited the opposite phenomenon (P < 0.05). Further research revealed that Bcl2 set as a direct downstream target of miR-148-3p. Our study firstly confirmed that, miR-148-3p might play a crucial role in tumorigenesis, as well as development of gastric cancer by targeting Bcl2, and could become a promising target for gastric cancer treatment.

胃癌(GC)是全球第四大常见癌症。本研究旨在探讨 miR-148-3p 对胃癌的生物学效应。研究利用定量反转录聚合酶链反应(RT-qPCR)分析了 miR-148-3p 在 GC 细胞系中的 mRNA 表达。将 miR-148-3p 的模拟物和抑制剂小心地转染到 GC 细胞中,以上调或下调 miR-148-3p 的表达。观察 miR-148-3p 表达变化对 GC 细胞增殖、集落形成、肿瘤发生、化疗敏感性、跨孔迁移和侵袭的影响。利用在线数据库工具预测 miR-148-3p 有希望的靶点,并通过 RT-qPCR、Western 印迹和荧光素酶报告进行验证。我们发现,miR-148-3p 在 GC 细胞中的表达水平明显下调(P
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引用次数: 0
Exopolysaccharide from marine microalgae belonging to the Glossomastix genus: fragile gel behavior and suspension stability. 来自 Glossomastix 属海洋微藻的外多糖:脆弱凝胶行为和悬浮稳定性。
IF 4.9 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2023-12-28 DOI: 10.1080/21655979.2023.2296257
Virginie Dulong, Christophe Rihouey, Clément Gaignard, Nicolas Bridiau, Priscilla Gourvil, Céline Laroche, Guillaume Pierre, Tony Varacavoudin, Ian Probert, Thierry Maugard, Philippe Michaud, Luc Picton, Didier Le Cerf

With the aim to find new polysaccharides of rheological interest with innovated properties, rhamnofucans produced as exopolysaccharides (EPS) in a photobioreactor (PBR) and an airlift bioreactor (ABR) by the marine microalgae Glossomastix sp. RCC3707 and RCC3688 were fully studied. Chemical characterizations have been conducted (UHPLC - MS HR). Analyses by size-exclusion chromatography (SEC) coupled online with a multiangle light scattering detector (MALS) and a differential refractive index detector showed the presence of large structures with molar masses higher than 106 g.mol-1. The rheological studies of these EPS solutions, conducted at different concentrations and salinities, have evidenced interesting and rare behavior characteristic of weak and fragile hydrogels i.e. gel behavior with very low elastic moduli (between 10-2 and 10 Pa) and yield stresses (between 10-2 and 2 Pa) according to the EPS source, concentration, and salinity. These results were confirmed by diffusing wave spectroscopy. Finally, as one of potential application, solutions of EPS from Glossomastix sp. have evidenced very good properties as anti-settling stabilizers, using microcrystalline cellulose particles as model, studied by multiple light scattering (MLS) with utilization in cosmetic or food industry. Compared to alginate solution with same viscosity for which sedimentation is observed over few hours, microalgae EPS leads to a stable suspension over few days.

为了找到具有创新特性的新型流变多糖,我们对海洋微藻 Glossomastix sp. RCC3707 和 RCC3688 在光生物反应器(PBR)和气提生物反应器(ABR)中生产的鼠李糖外多糖(EPS)进行了全面研究。进行了化学特性分析(超高效液相色谱-质谱 HR)。通过尺寸排阻色谱法(SEC)与多角度光散射检测器(MALS)和微分折射率检测器联机进行的分析表明,存在摩尔质量高于 106 g.mol-1 的大型结构。在不同浓度和盐度下对这些 EPS 溶液进行的流变学研究表明,这些溶液具有有趣且罕见的弱脆性水凝胶特征,即根据 EPS 来源、浓度和盐度的不同,凝胶行为具有极低的弹性模量(介于 10-2 和 10 Pa 之间)和屈服应力(介于 10-2 和 2 Pa 之间)。扩散波光谱法证实了这些结果。最后,作为潜在的应用之一,以微晶纤维素颗粒为模型,通过多重光散射(MLS)研究发现 Glossomastix sp.的 EPS 溶液具有很好的防沉降稳定剂特性,可用于化妆品或食品工业。与相同粘度的海藻酸溶液相比,海藻发泡聚苯乙烯可在数小时内形成沉淀,而微藻发泡聚苯乙烯则可在数天内形成稳定的悬浮液。
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引用次数: 0
Statement of Retraction: microRNA-10a-5p from gastric cancer cell-derived exosomes enhances viability and migration of human umbilical vein endothelial cells by targeting zinc finger MYND-type containing 11. 撤回声明:胃癌细胞衍生外泌体中的microRNA-10a-5p通过靶向含锌手指MYND型11增强人脐静脉内皮细胞的活力和迁移。
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299590
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引用次数: 0
Statement of Retraction: miR-188-3p abolishes germacrone-mediated podocyte protection in a mouse model of diabetic nephropathy in type I diabetes through triggering mitochondrial injury. 撤稿声明:在 I 型糖尿病肾病小鼠模型中,miR-188-3p 通过引发线粒体损伤取消了胚芽鞘介导的荚膜细胞保护作用。
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299558
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引用次数: 0
Statement of Retraction: The myocardial infarction-associated transcript 2 inhibits lipid accumulation and promotes cholesterol efflux in oxidized low-density lipoprotein-induced THP-1-derived macrophages via inhibiting mitogen-activated protein kinase signaling and activating the nuclear factor erythroid-related factor 2 signaling pathway. 撤回声明:心肌梗死相关转录本 2 通过抑制丝裂原活化蛋白激酶信号传导和激活核因子红细胞相关因子 2 信号传导途径,抑制氧化低密度脂蛋白诱导的 THP-1 衍生巨噬细胞中的脂质积累并促进胆固醇外流。
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299617
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引用次数: 0
Statement of Retraction: Long non-coding RNA HOXA11 antisense RNA upregulates spermatogenesis-associated serine-rich 2-like to enhance cisplatin resistance in laryngeal squamous cell carcinoma by suppressing microRNA-518a. 撤回声明:长非编码RNA HOXA11反义RNA通过抑制microRNA-518a上调精子发生相关的富丝氨酸2样来增强喉鳞状细胞癌的顺铂耐药性。
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299591
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引用次数: 0
Statement of Retraction: Long non-coding RNA muscleblind like splicing regulator 1 antisense RNA 1 (LncRNA MBNL1-AS1) promotes the progression of acute myocardial infarction by regulating the microRNA-132-3p/SRY-related high-mobility-group box 4 (SOX4) axis. 撤回声明:长非编码RNA肌盲样剪接调节因子1反义RNA 1(LncRNA MBNL1-AS1)通过调节microRNA-132-3p/SRY相关的高迁移率组框4(SOX4)轴促进急性心肌梗死的进展。
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299561
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引用次数: 0
Statement of Retraction: Long non-coding RNA placentaspecific protein 2 regulates micorRNA-19a/tumor necrosis factor α to participate in polycystic ovary syndrome. 撤回声明:长非编码RNA胎盘特异性蛋白2调控micorRNA-19a/肿瘤坏死因子α参与多囊卵巢综合征的研究
IF 4.2 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299562
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引用次数: 0
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Bioengineered
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