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- Publisher Website: 10.1158/0008-5472.CAN-12-2991
- Scopus: eid_2-s2.0-84875981178
- PMID: 23382045
- WOS: WOS:000316995600029
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Article: A CD90+ Tumor-Initiating Cell Population with an Aggressive Signature and Metastatic Capacity in Esophageal Cancer
Title | A CD90+ Tumor-Initiating Cell Population with an Aggressive Signature and Metastatic Capacity in Esophageal Cancer |
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Authors | |
Issue Date | 2013 |
Publisher | American Association for Cancer Research. The Journal's web site is located at http://cancerres.aacrjournals.org/ |
Citation | Cancer Research, 2013, v. 73 n. 7, p. 2322-2332 How to Cite? |
Abstract | Tumor-initiating cells (TIC), also known as cancer stem cells, are regarded widely as a specific subpopulation of cells needed for cancer initiation and progression. TICs have yet to be identified in esophageal tumors that have an increasing incidence in developed countries. Here, we report a CD90 cell population found in esophageal squamous cell carcinoma (ESCC), which is endowed with stem cell-like properties and high tumorigenic and metastatic potential. mRNA profiling of these cells suggested pathways through which they drive tumor growth and metastasis, with deregulation of an Ets-1/MMP signaling pathway and epithelial-mesenchymal transition figuring prominently. These cells possessed higher self-renewal activity and were sufficient for tumor growth, differentiation, metastasis, and chemotherapeutic resistance. CD90 TICs were isolated and characterized from ESCC clinical specimens as well as ESCC cell lines. In freshly resected clinical specimens, they represented a rare cell population, the levels of which correlated with strong family histories and lymph node metastasis. Our results prompt further study of this CD90+ population of esophageal TICs as potential therapeutic targets. © 2012 American Association for Cancer Research. |
Persistent Identifier | http://hdl.handle.net/10722/183682 |
ISSN | 2023 Impact Factor: 12.5 2023 SCImago Journal Rankings: 3.468 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Tang, KH | - |
dc.contributor.author | Dai, YD | - |
dc.contributor.author | Tong, M | - |
dc.contributor.author | Chan, YP | - |
dc.contributor.author | Kwan, PS | - |
dc.contributor.author | Fu, L | - |
dc.contributor.author | Qin, YR | - |
dc.contributor.author | Tsao, GSW | - |
dc.contributor.author | Lung, HL | - |
dc.contributor.author | Lung, ML | - |
dc.contributor.author | Tong, DKH | - |
dc.contributor.author | Law, SYK | - |
dc.contributor.author | Chan, KW | - |
dc.contributor.author | Ma, SKY | - |
dc.contributor.author | Guan, X | - |
dc.date.accessioned | 2013-06-18T04:07:20Z | - |
dc.date.available | 2013-06-18T04:07:20Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Cancer Research, 2013, v. 73 n. 7, p. 2322-2332 | - |
dc.identifier.issn | 0008-5472 | - |
dc.identifier.uri | http://hdl.handle.net/10722/183682 | - |
dc.description.abstract | Tumor-initiating cells (TIC), also known as cancer stem cells, are regarded widely as a specific subpopulation of cells needed for cancer initiation and progression. TICs have yet to be identified in esophageal tumors that have an increasing incidence in developed countries. Here, we report a CD90 cell population found in esophageal squamous cell carcinoma (ESCC), which is endowed with stem cell-like properties and high tumorigenic and metastatic potential. mRNA profiling of these cells suggested pathways through which they drive tumor growth and metastasis, with deregulation of an Ets-1/MMP signaling pathway and epithelial-mesenchymal transition figuring prominently. These cells possessed higher self-renewal activity and were sufficient for tumor growth, differentiation, metastasis, and chemotherapeutic resistance. CD90 TICs were isolated and characterized from ESCC clinical specimens as well as ESCC cell lines. In freshly resected clinical specimens, they represented a rare cell population, the levels of which correlated with strong family histories and lymph node metastasis. Our results prompt further study of this CD90+ population of esophageal TICs as potential therapeutic targets. © 2012 American Association for Cancer Research. | - |
dc.language | eng | - |
dc.publisher | American Association for Cancer Research. The Journal's web site is located at http://cancerres.aacrjournals.org/ | - |
dc.relation.ispartof | Cancer Research | - |
dc.title | A CD90+ Tumor-Initiating Cell Population with an Aggressive Signature and Metastatic Capacity in Esophageal Cancer | - |
dc.type | Article | - |
dc.identifier.email | Tang, KH: h0422624@hkusua.hku.hk | - |
dc.identifier.email | Chan, YP: bchanyp@hkucc.hku.hk | - |
dc.identifier.email | Kwan, PS: kwanps@hku.hk | - |
dc.identifier.email | Fu, L: gracefu@graduate.hku.hk | - |
dc.identifier.email | Tsao, GSW: gswtsao@hku.hk | - |
dc.identifier.email | Lung, HL: hllung2@hku.hk | - |
dc.identifier.email | Lung, ML: mlilung@hku.hk | - |
dc.identifier.email | Tong, DKH: esodtong@hku.hk | - |
dc.identifier.email | Law, SYK: slaw@hku.hk | - |
dc.identifier.email | Chan, KW: hrmtckw@hku.hk | - |
dc.identifier.email | Ma, SKY: stefma@hku.hk | - |
dc.identifier.email | Guan, X: xyguan@hkucc.hku.hk | - |
dc.identifier.authority | Fu, L=rp01435 | - |
dc.identifier.authority | Tsao, GSW=rp00399 | - |
dc.identifier.authority | Lung, HL=rp00299 | - |
dc.identifier.authority | Lung, ML=rp00300 | - |
dc.identifier.authority | Law, SYK=rp00437 | - |
dc.identifier.authority | Chan, KW=rp00330 | - |
dc.identifier.authority | Ma, SKY=rp00506 | - |
dc.identifier.authority | Guan, X=rp00454 | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1158/0008-5472.CAN-12-2991 | - |
dc.identifier.pmid | 23382045 | - |
dc.identifier.scopus | eid_2-s2.0-84875981178 | - |
dc.identifier.hkuros | 214431 | - |
dc.identifier.volume | 73 | - |
dc.identifier.issue | 7 | - |
dc.identifier.spage | 2322 | - |
dc.identifier.epage | 2332 | - |
dc.identifier.isi | WOS:000316995600029 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0008-5472 | - |