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- Publisher Website: 10.1038/modpathol.2008.94
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- PMID: 18931653
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Article: The prognostic significance of BMP-6 signaling in prostate cancer
Title | The prognostic significance of BMP-6 signaling in prostate cancer |
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Authors | |
Keywords | BMP-6 Metastasis Noggin Prostate cancer Sclerostin |
Issue Date | 2008 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/modpathol/ |
Citation | Modern Pathology, 2008, v. 21 n. 12, p. 1436-1443 How to Cite? |
Abstract | The importance of bone-morphogenetic proteins in prostate cancer is well recognized. Bone-morphogenetic protein-6 overexpression has been shown to increase the aggressiveness and invasiveness of prostate cancer cells. Recent studies on noggin and sclerostin, potent inhibitors of bone-morphogenetic protein signaling, have found that noggin also modifies the ability of prostate cancer cells to metastasize to bone. Taken together, these results suggest that bone-morphogenetic protein-6 signaling is important in prostate cancer progression. Our study investigated the expression of bone-morphogenetic protein-6, noggin and sclerostin in human prostate specimens (n=136) by immunohistochemical staining. We found that bone-morphogenetic protein-6 was increased (P<0.001), whereas sclerostin was decreased (P=0.004) in prostate cancer compared with nodular hyperplasia. In addition, significantly higher level of bone-morphogenetic protein-6 expression was observed in high-grade prostate cancer with Gleason score ≥7 (P=0.027). Bone-morphogenetic protein-6, noggin and sclerostin alone could not predict the development of distant metastasis in our patient cohort. However, high level of bone-morphogenetic protein-6 and low level of noggin, or high level of bone-morphogenetic protein-6 and low level of both noggin and sclerostin expression in primary prostate cancer significantly predicted development of distant metastasis. The predictive value was still valid when only high-grade prostate cancers were included or when patients with secondary lesion other than bone were excluded. Taken together, these results suggest that a high level of bone-morphogenetic protein-6 signaling, resulting from increased expression of bone-morphogenetic protein-6 and decreased expression of its inhibitors, might promote the development of prostate cancer metastases. Our results also imply the potential use of bone-morphogenetic protein-6, noggin and sclerostin expression together as a prognostic predictor for metastatic progression of prostate cancer. © 2008 USCAP, Inc All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/148593 |
ISSN | 2023 Impact Factor: 7.1 2023 SCImago Journal Rankings: 2.328 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yuen, HF | en_HK |
dc.contributor.author | Chan, YP | en_HK |
dc.contributor.author | Cheung, WL | en_HK |
dc.contributor.author | Wong, YC | en_HK |
dc.contributor.author | Wang, X | en_HK |
dc.contributor.author | Chan, KW | en_HK |
dc.date.accessioned | 2012-05-29T06:13:57Z | - |
dc.date.available | 2012-05-29T06:13:57Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Modern Pathology, 2008, v. 21 n. 12, p. 1436-1443 | en_HK |
dc.identifier.issn | 0893-3952 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/148593 | - |
dc.description.abstract | The importance of bone-morphogenetic proteins in prostate cancer is well recognized. Bone-morphogenetic protein-6 overexpression has been shown to increase the aggressiveness and invasiveness of prostate cancer cells. Recent studies on noggin and sclerostin, potent inhibitors of bone-morphogenetic protein signaling, have found that noggin also modifies the ability of prostate cancer cells to metastasize to bone. Taken together, these results suggest that bone-morphogenetic protein-6 signaling is important in prostate cancer progression. Our study investigated the expression of bone-morphogenetic protein-6, noggin and sclerostin in human prostate specimens (n=136) by immunohistochemical staining. We found that bone-morphogenetic protein-6 was increased (P<0.001), whereas sclerostin was decreased (P=0.004) in prostate cancer compared with nodular hyperplasia. In addition, significantly higher level of bone-morphogenetic protein-6 expression was observed in high-grade prostate cancer with Gleason score ≥7 (P=0.027). Bone-morphogenetic protein-6, noggin and sclerostin alone could not predict the development of distant metastasis in our patient cohort. However, high level of bone-morphogenetic protein-6 and low level of noggin, or high level of bone-morphogenetic protein-6 and low level of both noggin and sclerostin expression in primary prostate cancer significantly predicted development of distant metastasis. The predictive value was still valid when only high-grade prostate cancers were included or when patients with secondary lesion other than bone were excluded. Taken together, these results suggest that a high level of bone-morphogenetic protein-6 signaling, resulting from increased expression of bone-morphogenetic protein-6 and decreased expression of its inhibitors, might promote the development of prostate cancer metastases. Our results also imply the potential use of bone-morphogenetic protein-6, noggin and sclerostin expression together as a prognostic predictor for metastatic progression of prostate cancer. © 2008 USCAP, Inc All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/modpathol/ | en_HK |
dc.relation.ispartof | Modern Pathology | en_HK |
dc.subject | BMP-6 | en_HK |
dc.subject | Metastasis | en_HK |
dc.subject | Noggin | en_HK |
dc.subject | Prostate cancer | en_HK |
dc.subject | Sclerostin | en_HK |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Bone Morphogenetic Protein 6 - Biosynthesis | en_US |
dc.subject.mesh | Bone Morphogenetic Proteins - Biosynthesis | en_US |
dc.subject.mesh | Carrier Proteins - Biosynthesis | en_US |
dc.subject.mesh | Disease Progression | en_US |
dc.subject.mesh | Genetic Markers | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | Kaplan-Meier Estimate | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Prostatic Neoplasms - Metabolism - Mortality - Pathology | en_US |
dc.subject.mesh | Signal Transduction - Physiology | en_US |
dc.subject.mesh | Tumor Markers, Biological - Analysis | en_US |
dc.title | The prognostic significance of BMP-6 signaling in prostate cancer | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Wong, YC:ycwong@hkucc.hku.hk | en_HK |
dc.identifier.email | Chan, KW:hrmtckw@hku.hk | en_HK |
dc.identifier.authority | Wong, YC=rp00316 | en_HK |
dc.identifier.authority | Chan, KW=rp00330 | en_HK |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1038/modpathol.2008.94 | en_HK |
dc.identifier.pmid | 18931653 | - |
dc.identifier.scopus | eid_2-s2.0-56649114367 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-56649114367&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 21 | en_HK |
dc.identifier.issue | 12 | en_HK |
dc.identifier.spage | 1436 | en_HK |
dc.identifier.epage | 1443 | en_HK |
dc.identifier.isi | WOS:000261109000004 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Yuen, HF=14018633400 | en_HK |
dc.identifier.scopusauthorid | Chan, YP=14009821700 | en_HK |
dc.identifier.scopusauthorid | Cheung, WL=7202742743 | en_HK |
dc.identifier.scopusauthorid | Wong, YC=7403041798 | en_HK |
dc.identifier.scopusauthorid | Wang, X=7501854829 | en_HK |
dc.identifier.scopusauthorid | Chan, KW=16444133100 | en_HK |
dc.identifier.citeulike | 3472405 | - |
dc.identifier.issnl | 0893-3952 | - |