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- Publisher Website: 10.1038/sj.bjc.6603377
- Scopus: eid_2-s2.0-33750202160
- PMID: 17047655
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Article: Association of decreased mitochondrial DNA content with ovarian cancer progression
Title | Association of decreased mitochondrial DNA content with ovarian cancer progression |
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Authors | |
Keywords | Copy number Mitochondrial DNA Ovarian carcinoma |
Issue Date | 2006 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/bjc |
Citation | British Journal Of Cancer, 2006, v. 95 n. 8, p. 1087-1091 How to Cite? |
Abstract | Mitochondrial DNA (mtDNA) content in ovarian carcinomas was assessed by quantitative PCR. Results show that mtDNA content in tumour cell was significantly higher than that in normal ovary. Change in mtDNA content was not related with patients' age or tumour stages. However, the average mtDNA copy number in pathological low-grade tumours was over two-fold higher than that in high-grade carcinomas (P=0.012). Moreover, type I carcinomas also had a significantly higher mtDNA copy number than in type II carcinomas (P=0.019). Change in mtDNA content might be an important genetic event in the progression of ovarian carcinomas. © 2006 Cancer Research UK. |
Persistent Identifier | http://hdl.handle.net/10722/87223 |
ISSN | 2023 Impact Factor: 6.4 2023 SCImago Journal Rankings: 3.000 |
PubMed Central ID | |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Wang, Y | en_HK |
dc.contributor.author | Liu, VWS | en_HK |
dc.contributor.author | Xue, WC | en_HK |
dc.contributor.author | Cheung, ANY | en_HK |
dc.contributor.author | Ngan, HYS | en_HK |
dc.date.accessioned | 2010-09-06T09:26:55Z | - |
dc.date.available | 2010-09-06T09:26:55Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | British Journal Of Cancer, 2006, v. 95 n. 8, p. 1087-1091 | en_HK |
dc.identifier.issn | 0007-0920 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/87223 | - |
dc.description.abstract | Mitochondrial DNA (mtDNA) content in ovarian carcinomas was assessed by quantitative PCR. Results show that mtDNA content in tumour cell was significantly higher than that in normal ovary. Change in mtDNA content was not related with patients' age or tumour stages. However, the average mtDNA copy number in pathological low-grade tumours was over two-fold higher than that in high-grade carcinomas (P=0.012). Moreover, type I carcinomas also had a significantly higher mtDNA copy number than in type II carcinomas (P=0.019). Change in mtDNA content might be an important genetic event in the progression of ovarian carcinomas. © 2006 Cancer Research UK. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/bjc | en_HK |
dc.relation.ispartof | British Journal of Cancer | en_HK |
dc.subject | Copy number | en_HK |
dc.subject | Mitochondrial DNA | en_HK |
dc.subject | Ovarian carcinoma | en_HK |
dc.subject.mesh | Adenocarcinoma, Clear Cell - genetics - pathology | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Cystadenocarcinoma, Mucinous - genetics - pathology | en_HK |
dc.subject.mesh | Cystadenocarcinoma, Serous - genetics - pathology | en_HK |
dc.subject.mesh | DNA Replication - genetics | en_HK |
dc.subject.mesh | DNA, Mitochondrial - genetics - metabolism | en_HK |
dc.subject.mesh | Disease Progression | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Gene Expression Regulation, Neoplastic | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Neoplasm Staging | en_HK |
dc.subject.mesh | Ovarian Neoplasms - genetics - pathology | en_HK |
dc.title | Association of decreased mitochondrial DNA content with ovarian cancer progression | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0007-0920&volume=95&spage=1087&epage=1097&date=2006&atitle=Association+of+decreased+mitochondrial+DNA+content+with+ovarian+cancer+progression | en_HK |
dc.identifier.email | Liu, VWS: vwsliu@hkusua.hku.hk | en_HK |
dc.identifier.email | Cheung, ANY: anycheun@hkucc.hku.hk | en_HK |
dc.identifier.email | Ngan, HYS: hysngan@hkucc.hku.hk | en_HK |
dc.identifier.authority | Liu, VWS=rp00341 | en_HK |
dc.identifier.authority | Cheung, ANY=rp00542 | en_HK |
dc.identifier.authority | Ngan, HYS=rp00346 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1038/sj.bjc.6603377 | en_HK |
dc.identifier.pmid | 17047655 | en_HK |
dc.identifier.pmcid | PMC2360719 | - |
dc.identifier.scopus | eid_2-s2.0-33750202160 | en_HK |
dc.identifier.hkuros | 130525 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33750202160&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 95 | en_HK |
dc.identifier.issue | 8 | en_HK |
dc.identifier.spage | 1087 | en_HK |
dc.identifier.epage | 1091 | en_HK |
dc.identifier.isi | WOS:000241384400022 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Wang, Y=49762386700 | en_HK |
dc.identifier.scopusauthorid | Liu, VWS=7006405113 | en_HK |
dc.identifier.scopusauthorid | Xue, WC=7103165268 | en_HK |
dc.identifier.scopusauthorid | Cheung, ANY=54927484100 | en_HK |
dc.identifier.scopusauthorid | Ngan, HYS=34571944100 | en_HK |
dc.identifier.issnl | 0007-0920 | - |