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Article: The prostate gland and prostate carcinogenesis.
Title | The prostate gland and prostate carcinogenesis. |
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Authors | |
Issue Date | 1998 |
Citation | Italian Journal Of Anatomy And Embryology = Archivio Italiano Di Anatomia Ed Embriologia, 1998, v. 103 n. 4 Suppl 1, p. 237-252 How to Cite? |
Abstract | Despite extensive research, the mechanisms of prostate carcinogenesis are not well understood. The slow progress in this area is due, at least in part, to lack of a suitable animal model for prostate carcinogenesis. We have developed an animal model, based on the existing sex hormone-induced prostate carcinogenesis in the Noble rat, by substantially increasing the dosage of testosterone while keeping the level of estrogen unchanged. Using the modified method of combination of testosterone and estradiol-17beta (T+E2), it has been shown in Noble rats that prostate carcinogenesis followed a multi-step process involving hyperplasia, dysplasia, and carcinoma. We have demonstrated the importance of TGF-alpha, TGF-beta1 and bFGF in the development of prostate carcinogenesis. This study also established the roles of VEGF and IGF-1, initially as paracrine factors in epithelial-stromal interactions during the process of carcinogenesis and subsequently switching over to an autocrine mode during the establishment of carcinoma. |
Persistent Identifier | http://hdl.handle.net/10722/149572 |
ISSN | 2023 SCImago Journal Rankings: 0.127 |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wong, YC | en_US |
dc.contributor.author | Wang, YZ | en_US |
dc.contributor.author | Tam, NN | en_US |
dc.date.accessioned | 2012-06-26T05:55:25Z | - |
dc.date.available | 2012-06-26T05:55:25Z | - |
dc.date.issued | 1998 | en_US |
dc.identifier.citation | Italian Journal Of Anatomy And Embryology = Archivio Italiano Di Anatomia Ed Embriologia, 1998, v. 103 n. 4 Suppl 1, p. 237-252 | en_US |
dc.identifier.issn | 1122-6714 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/149572 | - |
dc.description.abstract | Despite extensive research, the mechanisms of prostate carcinogenesis are not well understood. The slow progress in this area is due, at least in part, to lack of a suitable animal model for prostate carcinogenesis. We have developed an animal model, based on the existing sex hormone-induced prostate carcinogenesis in the Noble rat, by substantially increasing the dosage of testosterone while keeping the level of estrogen unchanged. Using the modified method of combination of testosterone and estradiol-17beta (T+E2), it has been shown in Noble rats that prostate carcinogenesis followed a multi-step process involving hyperplasia, dysplasia, and carcinoma. We have demonstrated the importance of TGF-alpha, TGF-beta1 and bFGF in the development of prostate carcinogenesis. This study also established the roles of VEGF and IGF-1, initially as paracrine factors in epithelial-stromal interactions during the process of carcinogenesis and subsequently switching over to an autocrine mode during the establishment of carcinoma. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Italian journal of anatomy and embryology = Archivio italiano di anatomia ed embriologia | en_US |
dc.subject.mesh | Adenocarcinoma - Chemically Induced - Chemistry - Pathology | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Disease Models, Animal | en_US |
dc.subject.mesh | Dose-Response Relationship, Drug | en_US |
dc.subject.mesh | Drug Therapy, Combination | en_US |
dc.subject.mesh | Endothelial Growth Factors - Analysis | en_US |
dc.subject.mesh | Estradiol - Toxicity | en_US |
dc.subject.mesh | Fibroblast Growth Factor 2 - Analysis | en_US |
dc.subject.mesh | Hyperplasia - Chemically Induced - Pathology | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | Lymphokines - Analysis | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Precancerous Conditions - Chemically Induced - Pathology | en_US |
dc.subject.mesh | Prostate - Anatomy & Histology - Drug Effects - Pathology | en_US |
dc.subject.mesh | Prostatic Neoplasms - Chemically Induced - Chemistry - Pathology | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, Inbred Strains | en_US |
dc.subject.mesh | Receptor Protein-Tyrosine Kinases - Analysis | en_US |
dc.subject.mesh | Receptors, Growth Factor - Analysis | en_US |
dc.subject.mesh | Receptors, Vascular Endothelial Growth Factor | en_US |
dc.subject.mesh | Testosterone - Administration & Dosage - Toxicity | en_US |
dc.subject.mesh | Transforming Growth Factor Alpha - Analysis | en_US |
dc.subject.mesh | Transforming Growth Factor Beta - Analysis | en_US |
dc.subject.mesh | Transforming Growth Factor Beta1 | en_US |
dc.subject.mesh | Vascular Endothelial Growth Factor A | en_US |
dc.subject.mesh | Vascular Endothelial Growth Factors | en_US |
dc.title | The prostate gland and prostate carcinogenesis. | en_US |
dc.type | Article | en_US |
dc.identifier.email | Wong, YC:ycwong@hkucc.hku.hk | en_US |
dc.identifier.authority | Wong, YC=rp00316 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.pmid | 11315954 | - |
dc.identifier.scopus | eid_2-s2.0-0032229096 | en_US |
dc.identifier.hkuros | 46875 | - |
dc.identifier.volume | 103 | en_US |
dc.identifier.issue | 4 Suppl 1 | en_US |
dc.identifier.spage | 237 | en_US |
dc.identifier.epage | 252 | en_US |
dc.publisher.place | Italy | en_US |
dc.identifier.scopusauthorid | Wong, YC=7403041798 | en_US |
dc.identifier.scopusauthorid | Wang, YZ=8581934500 | en_US |
dc.identifier.scopusauthorid | Tam, NN=7101712624 | en_US |
dc.identifier.issnl | 1122-6714 | - |