Publications by authors named "Feng Cai"

p-Nitrobenzenesulfenyl chloride is a stable commercially available sulfenyl chloride that, in conjunction with silver triflate, cleanly activates a wide range of thioglycosides for glycosylation at -78 degrees C in CH(2)Cl(2).

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Objective: To investigate the expression of calcyclin in pancreatic carcinoma and its relation to the patients' prognosis.

Methods: Human pancreatic carcinoma tissue microarray was constructed, which contained 63 cores of 3 normal adult pancreas tissues, 6 chronic pancreatitis tissues, 51 pancreatic carcinoma tissues and 3 islet cell carcinoma tissues. Immunohistochemistry was performed to detect the expression of calcyclin in these tissues, and the relationship between calcyclin and the clinicopatholoical features of pancreatic carcinoma was analyzed.

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Objective: To study the technical method and clinical value of stent implantation through the rendezvous technique of percutaneous transhepatic biliary drainage (PTBD) and endoscopic retrograde cholangiopancreatography (ERCP) in patients with obstructive jaundice.

Methods: Thirty-six patients with obstructive jaundice underwent the rendezvous technique of PTBD and ERCP after initially unsuccessful ERCP.

Results: The procedure of 36 cases were all successful.

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Article Synopsis
  • Human PNAS-4 is a new protein that promotes cell death (apoptosis) in mammals, and researchers have now cloned and studied its counterpart (xPNAS-4) in a frog species, Xenopus laevis.
  • The xPNAS-4 protein was produced in E. coli, purified from insoluble forms, and refolded, yielding a highly pure protein suitable for further research.
  • This work also involved creating specific antibodies for xPNAS-4, enabling scientists to investigate its role and expression during embryonic development in frogs, marking the first discovery of this protein in this model organism.
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Purpose: With a widening arsenal of cancer therapies available, it is important to develop therapy-specific predictive markers and methods to rapidly assess treatment efficacy. We here evaluated the use of cytokeratin-18 (CK18) as a serum biomarker for monitoring chemotherapy-induced cell death in breast cancer.

Experimental Design: Different molecular forms of CK18 (caspase cleaved and total) were assessed by specific ELISA assays.

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[reaction: see text] The 2-O-[3-(2'-benzyloxyphenyl)-3,3-dimethylpropanoate] and 2-O-[3-(2'-benzyloxy-4',6'-dimethylphenyl)-3,3-dimethylpropanoate] esters enable the synthesis of a range of beta-glucosides and alpha-mannosides through neighboring participation in excellent yield, and are removed by hydrogenolysis in concert with the cleavage of benzyl esters in the presence of other esters making them particularly well suited to the stereocontrolled synthesis of glycosyl esters.

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Monoclonal antibodies have begun to show great clinical promise for the treatment of cancer. Antibodies that can directly affect a tumor cell's growth and/or survival are of particular interest for immunotherapy. Previously, we described monoclonal antibody DMF10.

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Background: Prostein is a recently described molecule expressed at the mRNA level in a prostate-specific manner. A murine monoclonal antibody was developed, characterized, and used to evaluate the expression of prostein protein in prostatic, other normal tissue and tumor samples.

Methods: The murine anti-prostein monoclonal antibody 10E3-G4-D3 was generated using recombinant prostein.

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Objective: To evaluate the clinical values of spiral CT imaging postprocessing techniques.

Methods: Totally 167 patients with known or suspected abnormalities of thorax (including small pulmonary emboli, primary and metastatic tumours, diffuse lung diseases, bronchiectasis and emphysema) underwent spiral CT of their thorax. We reconstructed images by using different postprocessing techniques (MPR, MIP, SSD, VR, STS and VE).

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Studies on the distribution and germination of Alexandrium sp. (A. tamarense + A.

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[reaction: see text] A short and highly stereoselective synthesis of the novel steroid squalamine (1) was accomplished in nine steps from easily available methyl chenodeoxylcholanate 2. Our synthesis featured improved dehydrogenation of 4 followed by conjugate reduction to construct the trans AB-ring system and efficient asymmetric isopropylation of aldehyde 6 to introduce the C-24R-hydroxyl group.

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A series of novel spermine dimer analogues was synthesized and assessed for their ability to inhibit spermidine transport into MDA-MB-231 breast carcinoma cells. Two spermine molecules were tethered via their N(1) primary amines with naphthalenedisulfonic acid, adamantanedicarboxylic acid and a series of aliphatic dicarboxylic acids. The linked spermine analogues were potent polyamine transport inhibitors and inhibited cell growth cytostatically in combination with a polyamine synthesis inhibitor.

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