File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.stem.2010.04.001
- Scopus: eid_2-s2.0-77956641496
- PMID: 20569697
- WOS: WOS:000278840700020
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: A subpopulation of CD26 + cancer stem cells with metastatic capacity in human colorectal cancer
Title | A subpopulation of CD26 + cancer stem cells with metastatic capacity in human colorectal cancer | ||||||||
---|---|---|---|---|---|---|---|---|---|
Authors | |||||||||
Keywords | Antigen Expression Cancer Combination Chemotherapy Cancer Stem Cell Cell Invasion Colorectal Cancer | ||||||||
Issue Date | 2010 | ||||||||
Publisher | Cell Press. The Journal's web site is located at http://www.cellstemcell.com | ||||||||
Citation | Cell Stem Cell, 2010, v. 6 n. 6, p. 603-615 How to Cite? | ||||||||
Abstract | Recent evidence suggests that a subpopulation of cancer cells, cancer stem cells (CSCs), is responsible for tumor growth in colorectal cancer. However, the role of CSCs in colorectal cancer metastasis is unclear. Here, we identified a subpopulation of CD26 + cells uniformly present in both the primary and metastatic tumors in colorectal cancer patients with liver metastasis. Furthermore, in patients without distant metastasis at the time of presentation, the presence of CD26 + cells in their primary tumors predicted distant metastasis on follow-up. Isolated CD26 + cells, but not CD26 - cells, led to development of distant metastasis when injected into the mouse cecal wall. CD26 + cells were also associated with enhanced invasiveness and chemoresistance. Our findings have uncovered a critical role of CSCs in metastatic progression of cancer. Furthermore, the ability to predict metastasis based on analysis of CSC subsets in the primary tumor may have important clinical implication as a selection criterion for adjuvant therapy. © 2010 Elsevier Inc. | ||||||||
Persistent Identifier | http://hdl.handle.net/10722/132475 | ||||||||
ISSN | 2023 Impact Factor: 19.8 2023 SCImago Journal Rankings: 10.253 | ||||||||
ISI Accession Number ID |
Funding Information: We thank A.M. Cheung for technical assistance in flow cytometry analysis, R. De Maria and X.W. Wang for critical discussion of the manuscript, A. Chan and S.Y. Fan for specimen collection, and G.S.W. Tsao for support. This study is supported by Strategic Research Theme of Cancer, Seed Funding Research Grant, and Donation of the Li Ka Shing Foundation of Matching Grants of The University of Hong Kong. | ||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Pang, R | en_HK |
dc.contributor.author | Law, WL | en_HK |
dc.contributor.author | Chu, ACY | en_HK |
dc.contributor.author | Poon, JT | en_HK |
dc.contributor.author | Lam, CSC | en_HK |
dc.contributor.author | Chow, AKM | en_HK |
dc.contributor.author | Ng, L | en_HK |
dc.contributor.author | Cheung, LWH | en_HK |
dc.contributor.author | Lan, XR | en_HK |
dc.contributor.author | Lan, HY | en_HK |
dc.contributor.author | Tan, VPY | en_HK |
dc.contributor.author | Yau, TC | en_HK |
dc.contributor.author | Poon, RT | en_HK |
dc.contributor.author | Wong, BCY | en_HK |
dc.date.accessioned | 2011-03-28T09:25:08Z | - |
dc.date.available | 2011-03-28T09:25:08Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Cell Stem Cell, 2010, v. 6 n. 6, p. 603-615 | en_HK |
dc.identifier.issn | 1934-5909 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/132475 | - |
dc.description.abstract | Recent evidence suggests that a subpopulation of cancer cells, cancer stem cells (CSCs), is responsible for tumor growth in colorectal cancer. However, the role of CSCs in colorectal cancer metastasis is unclear. Here, we identified a subpopulation of CD26 + cells uniformly present in both the primary and metastatic tumors in colorectal cancer patients with liver metastasis. Furthermore, in patients without distant metastasis at the time of presentation, the presence of CD26 + cells in their primary tumors predicted distant metastasis on follow-up. Isolated CD26 + cells, but not CD26 - cells, led to development of distant metastasis when injected into the mouse cecal wall. CD26 + cells were also associated with enhanced invasiveness and chemoresistance. Our findings have uncovered a critical role of CSCs in metastatic progression of cancer. Furthermore, the ability to predict metastasis based on analysis of CSC subsets in the primary tumor may have important clinical implication as a selection criterion for adjuvant therapy. © 2010 Elsevier Inc. | en_HK |
dc.language | eng | en_US |
dc.publisher | Cell Press. The Journal's web site is located at http://www.cellstemcell.com | en_HK |
dc.relation.ispartof | Cell Stem Cell | en_HK |
dc.subject | Antigen Expression | en_US |
dc.subject | Cancer Combination Chemotherapy | - |
dc.subject | Cancer Stem Cell | - |
dc.subject | Cell Invasion | - |
dc.subject | Colorectal Cancer | - |
dc.title | A subpopulation of CD26 + cancer stem cells with metastatic capacity in human colorectal cancer | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1934-5909&volume=6&issue=6&spage=603&epage=615&date=2010&atitle=A+subpopulation+of+CD26++cancer+stem+cells+with+metastatic+capacity+in+human+colorectal+cancer | - |
dc.identifier.email | Pang, R: robertap@hkucc.hku.hk | en_HK |
dc.identifier.email | Law, WL: lawwl@hkucc.hku.hk | en_HK |
dc.identifier.email | Poon, JT: tcjensen@hkucc.hku.hk | en_HK |
dc.identifier.email | Tan, VPY: vpytan@hku.hk | en_HK |
dc.identifier.email | Yau, TC: tyaucc@hku.hk | en_HK |
dc.identifier.email | Poon, RT: poontp@hkucc.hku.hk | en_HK |
dc.identifier.email | Wong, BCY: bcywong@hku.hk | en_HK |
dc.identifier.authority | Pang, R=rp00274 | en_HK |
dc.identifier.authority | Law, WL=rp00436 | en_HK |
dc.identifier.authority | Poon, JT=rp01603 | en_HK |
dc.identifier.authority | Tan, VPY=rp01458 | en_HK |
dc.identifier.authority | Yau, TC=rp01466 | en_HK |
dc.identifier.authority | Poon, RT=rp00446 | en_HK |
dc.identifier.authority | Wong, BCY=rp00429 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.stem.2010.04.001 | en_HK |
dc.identifier.pmid | 20569697 | - |
dc.identifier.scopus | eid_2-s2.0-77956641496 | en_HK |
dc.identifier.hkuros | 173427 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77956641496&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 6 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 603 | en_HK |
dc.identifier.epage | 615 | en_HK |
dc.identifier.isi | WOS:000278840700020 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Pang, R=7004376659 | en_HK |
dc.identifier.scopusauthorid | Law, WL=7103147867 | en_HK |
dc.identifier.scopusauthorid | Chu, ACY=36657034500 | en_HK |
dc.identifier.scopusauthorid | Poon, JT=7005903722 | en_HK |
dc.identifier.scopusauthorid | Lam, CSC=35332626500 | en_HK |
dc.identifier.scopusauthorid | Chow, AKM=36656984900 | en_HK |
dc.identifier.scopusauthorid | Ng, L=36450962500 | en_HK |
dc.identifier.scopusauthorid | Cheung, LWH=36656866300 | en_HK |
dc.identifier.scopusauthorid | Lan, XR=36657568600 | en_HK |
dc.identifier.scopusauthorid | Lan, HY=24544799000 | en_HK |
dc.identifier.scopusauthorid | Tan, VPY=24449627600 | en_HK |
dc.identifier.scopusauthorid | Yau, TC=23391533100 | en_HK |
dc.identifier.scopusauthorid | Poon, RT=7103097223 | en_HK |
dc.identifier.scopusauthorid | Wong, BCY=7402023340 | en_HK |
dc.identifier.issnl | 1875-9777 | - |