scholarly journals miR‑224‑5p regulates the proliferation, migration and invasion of pancreatic mucinous cystadenocarcinoma by targeting PTEN

2021 ◽  
Vol 23 (5) ◽  
Author(s):  
Xiaobo Peng ◽  
Chengtao Guo ◽  
Yanjun Wu ◽  
Mingzhen Ying ◽  
Renxu Chang ◽  
...  
Keyword(s):  
Mucinous Cystadenocarcinoma ◽  
Migration And Invasion

scholarly journals Autophagy promotes malignant migration and invasion via miR‑224‑5p/BCL2 in pancreatic mucinous cystadenocarcinoma MCC1 cells

2020 ◽  
Vol 20 (5) ◽  
pp. 1-1
Author(s):  
Chengtao Guo ◽  
Xiaobo Peng ◽  
Lele Song ◽  
Mingzhen Ying ◽  
Yanjun Wu ◽  
...  
Keyword(s):  
Mucinous Cystadenocarcinoma ◽  
Migration And Invasion

723: Chemokine Receptor CXCR4 Mediates Migration and Invasion of Bladder Cancer Cells

2004 ◽  
Vol 171 (4S) ◽  
pp. 192-192 ◽  
Author(s):  
Margitta Retz ◽  
Sukhvinder S. Sidhu ◽  
Gregory M. Dolganov ◽  
Jan Lehmann ◽  
Peter R. Carroll ◽  
...  
Keyword(s):  
Bladder Cancer ◽  
Cancer Cells ◽  
Chemokine Receptor ◽  
Migration And Invasion ◽  
Chemokine Receptor Cxcr4 ◽  
Bladder Cancer Cells

The Migration of Human Smooth Muscle Cells In Vitro Is Mediated by Plasminogen Activation and Can Be Inhibited by α2-Macroglobulin Receptor Associated Protein

1997 ◽  
Vol 78 (02) ◽  
pp. 880-886 ◽  
Author(s):  
Monique J Wijnberg ◽  
Paul H A Quax ◽  
Nancy M E Nieuwenbroek ◽  
Jan H Verheijen
Keyword(s):  
Smooth Muscle ◽  
Cell Migration ◽  
Smooth Muscle Cell ◽  
Muscle Cell ◽  
Ldl Receptor ◽  
Migration And Invasion ◽  
Invasion Assay ◽  
Plasminogen Activation ◽  
Smooth Muscle Cell Migration

SummaryThe plasminogen activation system is thought to be important in cell migration processes. A role for this system during smooth muscle cell migration after vascular injury has been suggested from several animal studies. However, not much is known about its involvement in human vascular remodelling. We studied the involvement of the plasminogen activation system in human smooth muscle cell migration in more detail using an in vitro wound assay and a matrix invasion assay. Inhibition of plasmin activity or inhibition of urokinase-type plasminogen activator (u-PA) activity resulted in approximately 40% reduction of migration after 24 h in the wound assay and an even stronger reduction (70-80%) in the matrix invasion assay. Migration of smooth muscle cells in the presence of inhibitory antibodies against tissue-type plasminogen activator (t-PA) was not significantly reduced after 24 h, but after 48 h a 30% reduction of migration was observed, whereas in the matrix invasion assay a 50% reduction in invasion was observed already after 24 h. Prevention of the interaction of u-PA with cell surface receptors by addition of soluble u-PA receptor or α2-macroglobulin receptor associated protein (RAP) to the culture medium, resulted in a similar inhibition of migration and invasion. From these results it can be concluded that both u-PA and t-PA mediated plasminogen activation can contribute to in vitro human smooth muscle cell migration and invasion. Furthermore, the interaction between u-PA and its cell surface receptor appears also to be involved in this migration and invasion process. The inhibitory effects on migration and invasion by the addition of RAP suggests an involvement of a RAP sensitive receptor of the LDL receptor family, possibly the LDL-receptor related protein (LRP) and/or the VLDL receptor.

Pancreatic Mucinous Cystadenocarcinoma in an 11-year-old Girl: A Case Report

1999 ◽  
Vol 41 (1) ◽  
pp. 177
Author(s):  
Kyung Jae Jun ◽  
Bokyung Han ◽  
Hye Kyung Yoon ◽  
Sung Wook Shin
Keyword(s):  
Case Report ◽  
Mucinous Cystadenocarcinoma

miR-20a-enhanced cell migration and invasion via ATg5 in osteosarcoma

2020 ◽  
Vol 44 (4) ◽  
Author(s):  
Huaming Wang ◽  
Jie Yin ◽  
Jin Huang ◽  
Zongwei Liu ◽  
Shengtai Pei
Keyword(s):  
Cell Migration ◽  
Migration And Invasion ◽  
Cell Migration And Invasion

Primary mucinous cystadenocarcinoma of the breast: report of a rare case

2018 ◽  
Author(s):  
Elli Botsfari ◽  
Persefoni Xirou
Keyword(s):  
Rare Case ◽  
Mucinous Cystadenocarcinoma
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