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- Publisher Website: 10.1111/j.1440-1746.2009.05813.x
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- PMID: 19368632
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Article: Role and significance of focal adhesion proteins in hepatocellular carcinoma
Title | Role and significance of focal adhesion proteins in hepatocellular carcinoma | ||||
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Authors | |||||
Keywords | Clinicopathological significance Focal adhesion proteins Hepatocellular carcinoma Signaling pathways | ||||
Issue Date | 2009 | ||||
Publisher | Blackwell Publishing Asia | ||||
Citation | Journal Of Gastroenterology And Hepatology, 2009, v. 24 n. 4, p. 520-530 How to Cite? | ||||
Abstract | Focal adhesions are structural links between the extracellular matrix and actin cytoskeleton. They are important sites where dynamic alterations of proteins in the focal contacts are involved during cell movement. Focal adhesions are composed of diverse molecules, for instance, receptors, structural proteins, adaptors, GTPase, kinases and phosphatases. These molecules play critical roles in normal physiological events such as cellular adhesion, movement, cytoskeletal structure and intracellular signaling pathways. In cancers, aberrant expression and altered functions of focal adhesion proteins contribute to adverse tumor behavior. It is evident that these proteins do not function alone, but rather associate and work together in the process of tumor development and cancer metastasis. Focal adhesion proteins have been shown to play critical roles in hepatocellular carcinoma. Understanding the molecular interactions and mechanisms of the interconnected focal adhesion proteins is of particular importance in understanding mechanisms underlying hepatocellular carcinoma progression and development of potential effective treatment. © 2009 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd. | ||||
Persistent Identifier | http://hdl.handle.net/10722/60561 | ||||
ISSN | 2023 Impact Factor: 3.7 2023 SCImago Journal Rankings: 1.179 | ||||
ISI Accession Number ID |
Funding Information: The study was funded in part by the Hong Kong Research Grants Council (HKU7798/07M, HKU 7674/06M and HKU 1/06C). I.O.L.N. is Loke Yew Professor in Pathology. | ||||
References | |||||
Grants |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yam, JWP | en_HK |
dc.contributor.author | Tse, EYT | en_HK |
dc.contributor.author | Ng, IOL | en_HK |
dc.date.accessioned | 2010-05-31T04:13:42Z | - |
dc.date.available | 2010-05-31T04:13:42Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Journal Of Gastroenterology And Hepatology, 2009, v. 24 n. 4, p. 520-530 | en_HK |
dc.identifier.issn | 0815-9319 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/60561 | - |
dc.description.abstract | Focal adhesions are structural links between the extracellular matrix and actin cytoskeleton. They are important sites where dynamic alterations of proteins in the focal contacts are involved during cell movement. Focal adhesions are composed of diverse molecules, for instance, receptors, structural proteins, adaptors, GTPase, kinases and phosphatases. These molecules play critical roles in normal physiological events such as cellular adhesion, movement, cytoskeletal structure and intracellular signaling pathways. In cancers, aberrant expression and altered functions of focal adhesion proteins contribute to adverse tumor behavior. It is evident that these proteins do not function alone, but rather associate and work together in the process of tumor development and cancer metastasis. Focal adhesion proteins have been shown to play critical roles in hepatocellular carcinoma. Understanding the molecular interactions and mechanisms of the interconnected focal adhesion proteins is of particular importance in understanding mechanisms underlying hepatocellular carcinoma progression and development of potential effective treatment. © 2009 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Asia | en_HK |
dc.relation.ispartof | Journal of Gastroenterology and Hepatology | en_HK |
dc.subject | Clinicopathological significance | - |
dc.subject | Focal adhesion proteins | - |
dc.subject | Hepatocellular carcinoma | - |
dc.subject | Signaling pathways | - |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Carcinoma, Hepatocellular - metabolism - pathology | en_HK |
dc.subject.mesh | Cell Transformation, Neoplastic - metabolism | en_HK |
dc.subject.mesh | Focal Adhesions - enzymology - metabolism | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Liver Neoplasms - metabolism - pathology | en_HK |
dc.subject.mesh | Neoplasm Proteins - metabolism | en_HK |
dc.subject.mesh | Prognosis | en_HK |
dc.subject.mesh | Signal Transduction | en_HK |
dc.title | Role and significance of focal adhesion proteins in hepatocellular carcinoma | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0815-9319&volume=24&spage=520&epage=530&date=2009&atitle=Role+and+significance+of+focal+adhesion+proteins+in+hepatocellular+carcinoma | en_HK |
dc.identifier.email | Yam, JWP:judyyam@pathology.hku.hk | en_HK |
dc.identifier.email | Ng, IOL:iolng@hkucc.hku.hk | en_HK |
dc.identifier.authority | Yam, JWP=rp00468 | en_HK |
dc.identifier.authority | Ng, IOL=rp00335 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/j.1440-1746.2009.05813.x | en_HK |
dc.identifier.pmid | 19368632 | - |
dc.identifier.scopus | eid_2-s2.0-63849216628 | en_HK |
dc.identifier.hkuros | 159511 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-63849216628&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 24 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 520 | en_HK |
dc.identifier.epage | 530 | en_HK |
dc.identifier.isi | WOS:000264735400006 | - |
dc.publisher.place | Australia | en_HK |
dc.relation.project | Molecular pathology of liver cancer - a multidisciplinary study | - |
dc.relation.project | Characterization of tensin2, the binding partner of DLC1 tumor suppressor in liver cancer | - |
dc.identifier.citeulike | 4267096 | - |
dc.identifier.issnl | 0815-9319 | - |