2007
DOI: 10.1021/pr060644r
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Proteome Analysis and Tissue Microarray for Profiling Protein Markers Associated with Lymph Node Metastasis in Colorectal Cancer

Abstract: The techniques of proteomic analysis combined with tissue microarray provide us a dramatic tool for screening of LNM-associated proteins in cancer research. The increased expression of HSP-27, GST, and Annexin II, but decreased expression of L-FABP, suggests a significantly elevated incidence of LNM in CRC.

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Cited by 90 publications
(96 citation statements)
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“…To some extent, this result is consistent with the data reported by other groups, who listed several proteins involved in protein synthesis and folding (heat shock proteins), cellular reorganization and cytoskeleton (actin, tubulin), intracellular calciumbinding protein (calgranulin), and cell communication and signal transduction (annexin) in the proteomic profiles of colorectal cancer cell line and tissue. [27][28][29][30] However, there are still some different proteins between our data and other researchers' reports. 31,32 First, we consider that two-dimensional electrophoresis and MALDI-TOF MS-based PMF analysis for human tissue is more complex than that for cell line.…”
Section: Discussionmentioning
confidence: 56%
“…To some extent, this result is consistent with the data reported by other groups, who listed several proteins involved in protein synthesis and folding (heat shock proteins), cellular reorganization and cytoskeleton (actin, tubulin), intracellular calciumbinding protein (calgranulin), and cell communication and signal transduction (annexin) in the proteomic profiles of colorectal cancer cell line and tissue. [27][28][29][30] However, there are still some different proteins between our data and other researchers' reports. 31,32 First, we consider that two-dimensional electrophoresis and MALDI-TOF MS-based PMF analysis for human tissue is more complex than that for cell line.…”
Section: Discussionmentioning
confidence: 56%
“…To further analyze the degree of interstitial collagen deposition, Masson's trichrome-stained sections were graded as that in a previous report (9). Following an antigen retrieval by 6.5 mM citrate buffer (pH 6.0) pressure cooking and endogenous peroxidase activity blockage with 3% hydrogen peroxide in methanol for 20 min at room temperature, DAB immunohistochemistry staining was processed with the DAKO EnVision System (37). In brief, the slides were incubated with the primary antibody against collagen ␣ 1(I) or ␣-SMA overnight at 4°C, and then treated with a pepsin-based antigen retrieval technique.…”
Section: Methodsmentioning
confidence: 99%
“…Briefly, following a brief proteolytic digestion and a peroxidase blocking of tissue slides, the slides were incubated with the primary antibody against the respective target protein at a dilution of 1:500 overnight at 40°C. After PBS washing, peroxidase labeled polymer and substrate-chromogen were then employed in order to visualize the staining of the protein of interest [27]. Immunohistochemical staining was performed at the pathology department of the National Hepatobiliary and Enteric Surgery Research Center, Ministry of Health, China.…”
Section: Methodsmentioning
confidence: 99%