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121.
Lee CH 《Applied microbiology and biotechnology》2012,93(2):517-523
One of the primary limitations of cancer therapy is lack of selectivity of therapeutic agents to tumor cells. Current efforts
are focused on discovering and developing anticancer agents that selectively target only tumor cells and spare normal cells
to improve the therapeutic index. The use of preferentially replicating bacteria as an oncolytic agent is one of the innovative
approaches for the treatment of cancer. This is based on the observation that some obligate or facultative anaerobic bacteria
are capable of multiplying selectively in tumors and inhibiting their growth. Meanwhile, bacteria have been demonstrated to
colonize and destroy tumor, and have emerged as biological gene vectors to tumor microenvironment. To improve the efficacy
and safety of the bacterial therapy, a further understanding of bacteria between with immune system is required. Furthermore,
we want to evaluate how bacterial infection facilitates the “bystander effect” of chemotherapeutic agent and assess if it
can be used for additional antitumor effect when combined with chemotherapy. This study may not only evaluate therapeutic
efficacy of bacteria for the treatment of cancer but also elucidate the mechanisms underlying antitumor activities mediated
by bacteria, which involve host immune responses and the cellular molecular responses. 相似文献
122.
Immune suppression remains a consistent obstacle to successful anti-tumor immune responses. As tumors develop, they create
a microenvironment that not only supports tumor growth and metastasis but also reduces potential adaptive immunity to tumor
antigens. Among the many components of this tumor microenvironment is a population of dendritic cells which exert profound
immune suppressive effects on T cells. In this review, we discuss our recent findings related to these tumor-associated dendritic
cells and how targeting them may serve to generate more durable anti-tumor immune responses. 相似文献
123.
Jay G. Forsythe Sloane L. English Rachel E. Simoneaux Arthur L. Weber 《Origins of life and evolution of the biosphere》2018,48(2):201-211
A one-pot method was developed for the preparation of a series of β-alanine standards of moderate size (2 to ≥12 residues) for studies concerning the prebiotic origins of peptides. The one-pot synthesis involved two sequential reactions: (1) dry-down self-condensation of β-alanine methyl ester, yielding β-alanine peptide methyl ester oligomers, and (2) subsequent hydrolysis of β-alanine peptide methyl ester oligomers, producing a series of β-alanine peptide standards. These standards were then spiked into a model prebiotic product mixture to confirm by HPLC the formation of β-alanine peptides under plausible reaction conditions. The simplicity of this approach suggests it can be used to prepare a variety of β-peptide standards for investigating differences between α- and β-peptides in the context of prebiotic chemistry. 相似文献
124.
Differential expression analysis for sequence count data 总被引:22,自引:0,他引:22
High-throughput sequencing assays such as RNA-Seq, ChIP-Seq or barcode counting provide quantitative readouts in the form
of count data. To infer differential signal in such data correctly and with good statistical power, estimation of data variability
throughout the dynamic range and a suitable error model are required. We propose a method based on the negative binomial distribution,
with variance and mean linked by local regression and present an implementation, DESeq, as an R/Bioconductor package. 相似文献
125.
Corti A 《Cellular and molecular neurobiology》2010,30(8):1163-1170
Chromogranin A (CgA) is an acidic glycoprotein belonging to a family of regulated secretory proteins stored in the dense core
granules of the adrenal medulla and of many other neuroendocrine cells and neurons. This protein is frequently used as a diagnostic
and prognostic serum marker for a range of neuroendocrine tumors. Circulating CgA is also increased in patients with other
diseases, including subpopulations of patients with non-neuroendocrine tumors, with important prognostic implications. A growing
body of evidence suggests that CgA is more than a diagnostic/prognostic marker for cancer patients. Indeed, results of in
vitro experiments and in vivo studies in animal models suggest that this protein and its fragments can affect several elements
of the tumor microenvironment, including fibroblasts and endothelial cells. In this article, recent findings implicating CgA
as a modulator of the tumor microenvironment and suggesting that abnormal secretion of CgA could play important roles in tumor
progression and response to therapy in cancer patients are reviewed and discussed. 相似文献
126.
Jang do S Lee HJ Lee B Hong BH Cha HJ Yoon J Lim K Yoon YJ Kim J Ree M Lee HC Choi KY 《FEBS letters》2006,580(17):4166-4171
Failure to detect the intermediate in spite of its existence often leads to the conclusion that two-state transition in the unfolding process of the protein can be justified. In contrast to the previous equilibrium unfolding experiment fitted to a two-state model by circular dichroism and fluorescence spectroscopies, an equilibrium unfolding intermediate of a dimeric ketosteroid isomerase (KSI) could be detected by small angle X-ray scattering (SAXS) and analytical ultracentrifugation. The sizes of KSI were determined to be 18.7A in 0M urea, 17.3A in 5.2M urea, and 25.1A in 7M urea by SAXS. The size of KSI in 5.2M urea was significantly decreased compared with those in 0M and 7M urea, suggesting the existence of a compact intermediate. Sedimentation velocity as obtained by ultracentrifugation confirmed that KSI in 5.2M urea is distinctly different from native and fully-unfolded forms. The sizes measured by pulse field gradient nuclear magnetic resonance (NMR) spectroscopy were consistent with those obtained by SAXS. Discrepancy of equilibrium unfolding studies between size measurement methods and optical spectroscopies might be due to the failure in detecting the intermediate by optical spectroscopic methods. Further characterization of the intermediate using (1)H NMR spectroscopy and Kratky plot supported the existence of a partially-folded form of KSI which is distinct from those of native and fully-unfolded KSIs. Taken together, our results suggest that the formation of a compact intermediate should precede the association of monomers prior to the dimerization process during the folding of KSI. 相似文献
127.
Rhamnolipids, produced by Pseudomonas aeruginosa, represent an important group of biosurfactants having various industrial, environmental, and medical applications. Current
methods for rhamnolipid quantification involve the use of strong hazardous acids/chemicals, indirect measurement of the concentration
of sugar moiety, or require the availability of expensive equipment (HPLC-MS). A safer, easier method that measures the whole
rhamnolipid molecules would significantly enhance strain selection, metabolic engineering, and process development for economical
rhamnolipid production. A semi-quantitative method was reported earlier to differentiate between the rhamnolipid-producing
and non-producing strains using agar plates containing methylene blue and cetyl trimethylammonium bromide (CTAB). In this
study, a rapid and simple method for rhamnolipid analysis was developed by systematically investigating the complexation of
rhamnolipids and methylene blue, with and without the presence of CTAB. The method relies on measuring the absorbance (at
638 nm) of the rhamnolipid−methylene blue complex that partitions into the chloroform phase. With P. aeruginosa fermentation samples, the applicability of this method was verified by comparison of the analysis results with those obtained
from the commonly used anthrone reaction technique. 相似文献
128.
利用一株分离自传统发酵酸马奶中的益生干酪乳杆菌(Lactobacillus casei Zhang)进行固态发酵(Solid State Fermentation,SSF)。以发酵物中的活菌数为主要指标,采用九因素四水平(L32(4^9))的正交试验优化固态发酵培养基,并在优化的培养基基础上研究不同的初始含水量及培养时间对Lactobacillus casei Zhang活菌数的影响。实验结果表明,在固态发酵培养基组成为4g豆粕、5g麸皮、0.6g乳清粉、0.3g葡萄糖、0.3g碳酸钙、0.02g硫酸铵、0.01g硫酸镁,初始含水量为55%的优化条件下,37℃发酵60h,发酵物中Lactobacillus casei Zhang活菌数可达到4.08×10^10CFU/g。 相似文献
129.
130.
Li W Tian H Li L Li S Yue W Chen Z Qi L Hu W Zhu Y Hao B Gao C Si L Gao F 《生物化学与生物物理学报(英文版)》2012,44(7):577-583
Lung cancer is the leading cause of cancer-related mortality all over the world. In recent years, pulmonary adenocarcinoma has surpassed squamous cell carcinoma in frequency and is the predominant form of lung cancer in many countries. Epidemiological investigations have shown an inverse relationship between garlic (Allium sativum) consumption and death rate from many cancers. Diallyl trisulfide (DATS) is one of the garlic-derived compounds (also known as: organosulfer compounds, OSC). DATS can induce apoptosis and inhibit the growth of many cancer cell lines. Our study demonstrated that the apoptotic incidents induced by DATS were a mitochondria-dependent caspase cascade through a significant decrease of the anti-apoptotic Bcl-2 that resulted in up-regulation of the ratio of Bax/Bcl-2 and the activity of caspase-3, -8, and -9. Eventually, DATS induced the apoptosis and inhibited the proliferation in a concentration- and time-dependent manner. Furthermore, by establishing an animal model of female BALB/c nude mice with A549 xenografts, we found that oral gavage of DATS significantly retarded growth of A549 xenografts in nude mice without causing weight loss or any other side effects compared with the control group. All the evidence both in vitro and in vivo suggested that DATS could be an ideal anti-cancer drug. 相似文献