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Journal ArticleDOI

CD151 Amplifies Signaling by Integrin α6β1 to PI3K and Induces the Epithelial–Mesenchymal Transition in HCC Cells

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TLDR
High expression levels of CD151 and α6 promote invasiveness of HCC cells, and either of these proteins, or PI3K signaling, might be targets for therapeutics for subgroups of patients with HCC.
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This article is published in Gastroenterology.The article was published on 2011-05-01. It has received 154 citations till now. The article focuses on the topics: Epithelial–mesenchymal transition & PI3K/AKT/mTOR pathway.

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Citations
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Journal ArticleDOI

Role of epithelial to mesenchymal transition in hepatocellular carcinoma

TL;DR: Some aspects of EMT are still elusive and further studies are required to better link the clinical management of HCC with biomarkers and targeted therapies related to EMT, as well as explaining the current limiting insights into EMT by snapshot analyses of H CC tissues.
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Galectin-1 induces hepatocellular carcinoma EMT and sorafenib resistance by activating FAK/PI3K/AKT signaling.

TL;DR: Clinically, the data suggest that Gal-1 may be a potential therapeutic target for HCC and a biomarker for predicting response to sorafenib treatment and the role and molecular mechanism ofGal-1 activity in hepatocellular carcinoma remain enigmatic.
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Circular RNA circTRIM33–12 acts as the sponge of MicroRNA-191 to suppress hepatocellular carcinoma progression

TL;DR: The important role of circTRIM33–12 in the proliferation, migration, invasion and immune evasion abilities of HCC cells is revealed and a new perspective on circRNAs in HCC progression is provided.
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LncRNA SNHG3 induces EMT and sorafenib resistance by modulating the miR-128/CD151 pathway in hepatocellular carcinoma.

TL;DR: Clinically, data suggest that SNHG3 may be a novel therapeutic target and a biomarker for predicting response to sorafenib treatment of HCC, and increased SNHg3 expression is correlated with poor HCC survival outcomes and sorAFenib response.
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αB-crystallin complexes with 14-3-3ζ to induce epithelial-mesenchymal transition and resistance to sorafenib in hepatocellular carcinoma

TL;DR: Clinically, the data suggest that the αB‐Crystallin‐14‐3‐3ζ complex acts synergistically to promote HCC progression by constitutively activating ERK signaling, and a biomarker for predicting sorafenib treatment response.
References
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Journal ArticleDOI

Epithelial-Mesenchymal Transitions in Development and Disease

TL;DR: The mesenchymal state is associated with the capacity of cells to migrate to distant organs and maintain stemness, allowing their subsequent differentiation into multiple cell types during development and the initiation of metastasis.
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The Epithelial-Mesenchymal Transition Generates Cells with Properties of Stem Cells

TL;DR: It is reported that the induction of an EMT in immortalized human mammary epithelial cells (HMLEs) results in the acquisition of mesenchymal traits and in the expression of stem-cell markers, and it is shown that those cells have an increased ability to form mammospheres, a property associated with mammARY epithelial stem cells.
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Dual regulation of Snail by GSK-3β-mediated phosphorylation in control of epithelial–mesenchymal transition

TL;DR: It is shown that GSK-3β binds to and phosphorylates Snail at two consensus motifs to dually regulate the function of this protein and together function as a molecular switch for many signalling pathways that lead to EMT.
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Integrin signalling during tumour progression.

TL;DR: During progression from tumour growth to metastasis, specific integrin signals enable cancer cells to detach from neighbouring cells, re-orientate their polarity during migration, and survive and proliferate in foreign microenvironments.
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Tetraspanin functions and associated microdomains.

TL;DR: Important new genetic evidence has now emerged, and is bolstered by new insights into the cell biology, signalling and biochemistry of tetraspanins, that provide a framework for better understanding of these mysterious molecules in the regulation of cellular processes.
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