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Article: MicroRNA expression, survival, and response to interferon in liver cancer
Title | MicroRNA expression, survival, and response to interferon in liver cancer | ||||
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Authors | |||||
Issue Date | 2009 | ||||
Publisher | Massachusetts Medical Society. The Journal's web site is located at http://content.nejm.org/ | ||||
Citation | New England Journal of Medicine, 2009, v. 361 n. 15, p. 1437-1447 How to Cite? | ||||
Abstract | BACKGROUND: Hepatocellular carcinoma is a common and aggressive cancer that occurs mainly in men. We examined microRNA expression patterns, survival, and response to interferon alfa in both men and women with the disease. METHODS: We analyzed three independent cohorts that included a total of 455 patients with hepatocellular carcinoma who had undergone radical tumor resection between 1999 and 2003. MicroRNA-expression profiling was performed in a cohort of 241 patients with hepatocellular carcinoma to identify tumor-related microRNAs and determine their association with survival in men and women. In addition, to validate our findings, we used quantitative reverse-transcriptase-polymerase- chain-reaction assays to measure microRNAs and assess their association with survival and response to therapy with interferon alfa in 214 patients from two independent, prospective, randomized, controlled trials of adjuvant interferon therapy. RESULTS: In patients with hepatocellular carcinoma, the expression of miR-26a and miR-26b in nontumor liver tissue was higher in women than in men. Tumors had reduced levels of miR-26 expression, as compared with paired noncancerous tissues, which indicated that the level of miR-26 expression was also associated with hepatocellular carcinoma. Moreover, tumors with reduced miR-26 expression had a distinct transcriptomic pattern, and analyses of gene networks revealed that activation of signaling pathways between nuclear factor κB and interleukin-6 might play a role in tumor development. Patients whose tumors had low miR-26 expression had shorter overall survival but a better response to interferon therapy than did patients whose tumors had high expression of the microRNA. CONCLUSIONS: The expression patterns of microRNAs in liver tissue differ between men and women with hepatocellular carcinoma. The miR-26 expression status of such patients is associated with survival and response to adjuvant therapy with interferon alfa. Copyright © 2009 Massachusetts Medical Society. All rights reserved. | ||||
Persistent Identifier | http://hdl.handle.net/10722/88347 | ||||
ISSN | 2023 Impact Factor: 96.2 2023 SCImago Journal Rankings: 20.544 | ||||
PubMed Central ID | |||||
ISI Accession Number ID |
Funding Information: Supported in part by grants (Z01-BC 010313 and Z01-BC 010876) from the Intramural Research Program of the Center for Cancer Research of the National Cancer Institute. | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ji, J | en_HK |
dc.contributor.author | Shi, J | en_HK |
dc.contributor.author | Budhu, A | en_HK |
dc.contributor.author | Yu, Z | en_HK |
dc.contributor.author | Forgues, M | en_HK |
dc.contributor.author | Roessler, S | en_HK |
dc.contributor.author | Ambs, S | en_HK |
dc.contributor.author | Chen, Y | en_HK |
dc.contributor.author | Meltzer, PS | en_HK |
dc.contributor.author | Croce, CM | en_HK |
dc.contributor.author | Qin, LX | en_HK |
dc.contributor.author | Man, K | en_HK |
dc.contributor.author | Lo, CM | en_HK |
dc.contributor.author | Lee, J | en_HK |
dc.contributor.author | Ng, IOL | en_HK |
dc.contributor.author | Fan, J | en_HK |
dc.contributor.author | Tang, ZY | en_HK |
dc.contributor.author | Sun, HC | en_HK |
dc.contributor.author | Wang, XW | en_HK |
dc.date.accessioned | 2010-09-06T09:42:11Z | - |
dc.date.available | 2010-09-06T09:42:11Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | New England Journal of Medicine, 2009, v. 361 n. 15, p. 1437-1447 | en_HK |
dc.identifier.issn | 0028-4793 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/88347 | - |
dc.description.abstract | BACKGROUND: Hepatocellular carcinoma is a common and aggressive cancer that occurs mainly in men. We examined microRNA expression patterns, survival, and response to interferon alfa in both men and women with the disease. METHODS: We analyzed three independent cohorts that included a total of 455 patients with hepatocellular carcinoma who had undergone radical tumor resection between 1999 and 2003. MicroRNA-expression profiling was performed in a cohort of 241 patients with hepatocellular carcinoma to identify tumor-related microRNAs and determine their association with survival in men and women. In addition, to validate our findings, we used quantitative reverse-transcriptase-polymerase- chain-reaction assays to measure microRNAs and assess their association with survival and response to therapy with interferon alfa in 214 patients from two independent, prospective, randomized, controlled trials of adjuvant interferon therapy. RESULTS: In patients with hepatocellular carcinoma, the expression of miR-26a and miR-26b in nontumor liver tissue was higher in women than in men. Tumors had reduced levels of miR-26 expression, as compared with paired noncancerous tissues, which indicated that the level of miR-26 expression was also associated with hepatocellular carcinoma. Moreover, tumors with reduced miR-26 expression had a distinct transcriptomic pattern, and analyses of gene networks revealed that activation of signaling pathways between nuclear factor κB and interleukin-6 might play a role in tumor development. Patients whose tumors had low miR-26 expression had shorter overall survival but a better response to interferon therapy than did patients whose tumors had high expression of the microRNA. CONCLUSIONS: The expression patterns of microRNAs in liver tissue differ between men and women with hepatocellular carcinoma. The miR-26 expression status of such patients is associated with survival and response to adjuvant therapy with interferon alfa. Copyright © 2009 Massachusetts Medical Society. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Massachusetts Medical Society. The Journal's web site is located at http://content.nejm.org/ | en_HK |
dc.relation.ispartof | New England Journal of Medicine | en_HK |
dc.rights | From New England Journal of Medicine, Junfang Ji, Jiong Shi, Anuradha Budhu, et al., MicroRNA expression, survival, and response to interferon in liver cancer, vol. 361, p. 1437-1447. Copyright © 2009 Massachusetts Medical Society. Reprinted with permission. | en_HK |
dc.subject.mesh | Antiviral Agents - therapeutic use | - |
dc.subject.mesh | Carcinoma, Hepatocellular - drug therapy - genetics - mortality | - |
dc.subject.mesh | Gene Expression | - |
dc.subject.mesh | Interferon-alpha - therapeutic use | - |
dc.subject.mesh | Liver Neoplasms - drug therapy - genetics - mortality | - |
dc.title | MicroRNA expression, survival, and response to interferon in liver cancer | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Man, K: kwanman@hkucc.hku.hk | en_HK |
dc.identifier.email | Lo, CM: chungmlo@hkucc.hku.hk | en_HK |
dc.identifier.email | Ng, IOL: iolng@hkucc.hku.hk | en_HK |
dc.identifier.authority | Man, K=rp00417 | en_HK |
dc.identifier.authority | Lo, CM=rp00412 | en_HK |
dc.identifier.authority | Ng, IOL=rp00335 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1056/NEJMoa0901282 | en_HK |
dc.identifier.pmid | 19812400 | - |
dc.identifier.pmcid | PMC2786938 | - |
dc.identifier.scopus | eid_2-s2.0-70349871321 | en_HK |
dc.identifier.hkuros | 168549 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-70349871321&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 361 | en_HK |
dc.identifier.issue | 15 | en_HK |
dc.identifier.spage | 1437 | en_HK |
dc.identifier.epage | 1447 | en_HK |
dc.identifier.isi | WOS:000270540000005 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.f1000 | 1382977 | - |
dc.identifier.scopusauthorid | Ji, J=7201362455 | en_HK |
dc.identifier.scopusauthorid | Shi, J=7404495464 | en_HK |
dc.identifier.scopusauthorid | Budhu, A=6507301846 | en_HK |
dc.identifier.scopusauthorid | Yu, Z=8770380900 | en_HK |
dc.identifier.scopusauthorid | Forgues, M=6602363144 | en_HK |
dc.identifier.scopusauthorid | Roessler, S=12243081900 | en_HK |
dc.identifier.scopusauthorid | Ambs, S=6602816824 | en_HK |
dc.identifier.scopusauthorid | Chen, Y=7601431107 | en_HK |
dc.identifier.scopusauthorid | Meltzer, PS=7102464641 | en_HK |
dc.identifier.scopusauthorid | Croce, CM=34569630600 | en_HK |
dc.identifier.scopusauthorid | Qin, LX=16747601200 | en_HK |
dc.identifier.scopusauthorid | Man, K=7101754072 | en_HK |
dc.identifier.scopusauthorid | Lo, CM=7401771672 | en_HK |
dc.identifier.scopusauthorid | Lee, J=36065603500 | en_HK |
dc.identifier.scopusauthorid | Ng, IOL=7102753722 | en_HK |
dc.identifier.scopusauthorid | Fan, J=7402794379 | en_HK |
dc.identifier.scopusauthorid | Tang, ZY=7403306295 | en_HK |
dc.identifier.scopusauthorid | Sun, HC=35723133900 | en_HK |
dc.identifier.scopusauthorid | Wang, XW=8712734700 | en_HK |
dc.identifier.citeulike | 5955877 | - |
dc.identifier.issnl | 0028-4793 | - |