Τετάρτη 20 Ιουνίου 2018

Gastrointestinal microecology: a crucial and potential target in acute pancreatitis

Abstract

In the early stage of acute pancreatitis (AP), abundant cytokines induced by local pancreatic inflammation enter the bloodstream, further cause systemic inflammatory response syndrome (SIRS) by "trigger effect", which eventually leads to multiple organ dysfunction syndrome (MODS). During SIRS and MODS, the intestinal barrier function was seriously damaged accompanied by the occurrence of gut-derived infection which forms a "second hit summit" by inflammatory overabundance. Gastrointestinal microecology, namely the biologic barrier, could be transformed into a pathogenic state, which is called microflora dysbiosis when interfered by the inflammatory stress during AP. More and more evidences indicate that gastrointestinal microflora dysbiosis plays a key role in "the second hit" induced by AP gut-derived infection. Therefore, the maintenance of gastrointestinal microecology balance is likely to provide an effective method in modulating systemic infection of AP. This article reviewed the progress of gastrointestinal microecology in AP to provide a reference for deeply understanding the pathogenic mechanisms of AP and identifying new therapeutic targets.



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Construction and characterization of regulated cycle inhibiting factors induced upon Tet-On system in human colon cancer cell lines

A previous study has proven that cycle inhibiting factors (Cifs) inhibit Cullin E3 ubiquitin ligases, resulting in cell cycle arrest. More importantly, Cifs are also involved in cancer progression by deamidating Nedd8. Here we aimed to explore a novel insight into the treatment implications of Cifs in colon cancers by Tet-on system. The anticancer activity of Cif by doxycycline induction was investigated in the colon cell lines based upon Tet-On system. The expression of Cif in the colon cancer cells was determined by western blot. Furthermore, the cell viability and flow cytometry analysis were respectively performed to evaluate the cell proliferation and survival of colon cells. More importantly, the p21 and p27 levels were also evaluated after the induction of Cif with Tet-On system. Multiple clones of colon cancer cells for doxycycline-regulated Cif expression were constructed for maintenance purposes including HCT116 and SW480 cell lines. The result of western blot displayed good inducibility of expressing Cif in the cell lines. The clones with CifWT preserved their transformed phenotype compared with the control group (clones with GFP or with CifC/A), in terms of the inhibition of cancer cell proliferation and survival. Furthermore, western blot analysis showed that p27 and p21 were accumulated in the clones with CifWT, compared with the colon cancer cell lines with GFP or with CifC/A. Using the Tet-On system, we developed an efficient approach toward generation of colon cancer cells induced with Cif. These engineered colons tightly controlled Cif expression in vitro, which is a good inducible model system for cancer treatment. *Liang Liu and Jianjiao Ni contributed equally to the writing of this article. Correspondence to Xinhong He, MD, PhD, Department of Interventional Radiology, Fudan University Shanghai Cancer Center, No. 270, Dong'an Road, Shanghai 200032, China Tel: +86 216 417 5590; fax: +86 64 049 870; e-mail: yangqi20002006@21cn.com Received January 11, 2018 Accepted May 5, 2018 Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.

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Association between common polymorphisms in ERCC gene and prognosis of osteosarcoma in patients treated with chemotherapy: a meta-analysis

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Corrigendum

Cancer Medicine, Volume 7, Issue 6, Page 2793-2793, June 2018.


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Corrigendum

Cancer Medicine, Volume 7, Issue 6, Page 2792-2792, June 2018.


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Issue Information

Cancer Medicine, Volume 7, Issue 6, Page 2219-2220, June 2018.


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Identification of differential expressed lncRNAs in human thyroid cancer by a genome‐wide analyses

Cancer Medicine, EarlyView.


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