Article: Recurrent Chromosomal Imbalances in Nonsmall Cell Lung Carcinoma: The Association between 1q Amplification and Tumor Recurrence
| Title | Recurrent Chromosomal Imbalances in Nonsmall Cell Lung Carcinoma: The Association between 1q Amplification and Tumor Recurrence |
|---|---|
| Authors | Tai, ALS1 Yan, WS2 Fang, Y2 Xie, D1 Sham, JST1 Guan, XY1 |
| Issue Date | 2004 |
| Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/28741 |
| Citation | Cancer, 2004, v. 100 n. 9, p. 1918-1927 [How to Cite?] DOI: http://dx.doi.org/10.1002/cncr.20190 |
| Abstract | BACKGROUND. Lung carcinoma is a leading cause of cancer deaths worldwide. To better understand this disease, the authors studied genetic alterations in nonsmall cell lung carcinoma (NSCLC) and the association between genetic changes and clinical features. METHODS. Genetic alterations in 30 patients with adenocarcinoma (AC) and 39 patients with squamous cell carcinoma (SCC) were analyzed by comparative genomic hybridization. The genetic changes in patients with AC and SCC were compared and the associations of these changes with clinical features were studied. RESULTS. A gain of 3q with a minimal amplified region at 3q25.3-qter was significantly higher in patients with SCC compared with patients with AC (72% vs. 27%; P < 0.001). A gain of 20q and loss of chromosome 9 were detected more frequently in patients with AC compared with patients with SCC (P < 0.05). Gains of 5p and 20q and loss of 5q were significantly correlated with an advanced stage of NSCLC (P < 0.05). Amplification of 1q was significantly associated with NSCLC recurrence (P = 0.04). CONCLUSIONS. The results of the current study suggested that different chromosomal aberrations may contribute to the types and pathologic stages of NSCLC. © 2004 American Cancer Society. |
| ISSN | 0008-543X 2011 Impact Factor: 4.771 2011 SCImago Journal Rankings: 0.578 |
| DOI | http://dx.doi.org/10.1002/cncr.20190 |
| ISI Accession Number ID | WOS:000220929000019 |
| References | References in Scopus |
| dc.contributor.author | Tai, ALS |
|---|---|
| dc.contributor.author | Yan, WS |
| dc.contributor.author | Fang, Y |
| dc.contributor.author | Xie, D |
| dc.contributor.author | Sham, JST |
| dc.contributor.author | Guan, XY |
| dc.date.accessioned | 2010-09-06T06:36:28Z |
| dc.date.available | 2010-09-06T06:36:28Z |
| dc.date.issued | 2004 |
| dc.description.abstract | BACKGROUND. Lung carcinoma is a leading cause of cancer deaths worldwide. To better understand this disease, the authors studied genetic alterations in nonsmall cell lung carcinoma (NSCLC) and the association between genetic changes and clinical features. METHODS. Genetic alterations in 30 patients with adenocarcinoma (AC) and 39 patients with squamous cell carcinoma (SCC) were analyzed by comparative genomic hybridization. The genetic changes in patients with AC and SCC were compared and the associations of these changes with clinical features were studied. RESULTS. A gain of 3q with a minimal amplified region at 3q25.3-qter was significantly higher in patients with SCC compared with patients with AC (72% vs. 27%; P < 0.001). A gain of 20q and loss of chromosome 9 were detected more frequently in patients with AC compared with patients with SCC (P < 0.05). Gains of 5p and 20q and loss of 5q were significantly correlated with an advanced stage of NSCLC (P < 0.05). Amplification of 1q was significantly associated with NSCLC recurrence (P = 0.04). CONCLUSIONS. The results of the current study suggested that different chromosomal aberrations may contribute to the types and pathologic stages of NSCLC. © 2004 American Cancer Society. |
| dc.description.nature | Link_to_OA_fulltext |
| dc.identifier.citation | Cancer, 2004, v. 100 n. 9, p. 1918-1927 [How to Cite?] DOI: http://dx.doi.org/10.1002/cncr.20190 |
| dc.identifier.doi | http://dx.doi.org/10.1002/cncr.20190 |
| dc.identifier.epage | 1927 |
| dc.identifier.hkuros | 115339 |
| dc.identifier.hkuros | 96139 |
| dc.identifier.isi | WOS:000220929000019 |
| dc.identifier.issn | 0008-543X 2011 Impact Factor: 4.771 2011 SCImago Journal Rankings: 0.578 |
| dc.identifier.issue | 9 |
| dc.identifier.openurl | ![]() |
| dc.identifier.pmid | 15112273 |
| dc.identifier.scopus | eid_2-s2.0-1942499002 |
| dc.identifier.spage | 1918 |
| dc.identifier.uri | http://hdl.handle.net/10722/71917 |
| dc.identifier.volume | 100 |
| dc.language | eng |
| dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/28741 |
| dc.publisher.place | United States |
| dc.relation.ispartof | Cancer |
| dc.relation.references | References in Scopus |
| dc.rights | Cancer. Copyright © John Wiley & Sons, Inc. |
| dc.subject.mesh | Adenocarcinoma - genetics - mortality - therapy |
| dc.subject.mesh | Adult |
| dc.subject.mesh | Aged |
| dc.subject.mesh | Blotting, Southern |
| dc.subject.mesh | Carcinoma, Non-Small-Cell Lung - genetics - mortality - therapy |
| dc.subject.mesh | Carcinoma, Squamous Cell - genetics - mortality - therapy |
| dc.subject.mesh | Chromosome Aberrations |
| dc.subject.mesh | Cohort Studies |
| dc.subject.mesh | Combined Modality Therapy |
| dc.subject.mesh | DNA, Neoplasm - analysis |
| dc.subject.mesh | Female |
| dc.subject.mesh | Humans |
| dc.subject.mesh | Lung Neoplasms - genetics - mortality - therapy |
| dc.subject.mesh | Male |
| dc.subject.mesh | Middle Aged |
| dc.subject.mesh | Neoplasm Recurrence, Local - epidemiology - genetics |
| dc.subject.mesh | Nucleic Acid Hybridization |
| dc.subject.mesh | Probability |
| dc.subject.mesh | Prognosis |
| dc.subject.mesh | Risk Assessment |
| dc.subject.mesh | Sensitivity and Specificity |
| dc.subject.mesh | Survival Analysis |
| dc.title | Recurrent Chromosomal Imbalances in Nonsmall Cell Lung Carcinoma: The Association between 1q Amplification and Tumor Recurrence |
| dc.type | Article |
Author Affiliations
- The University of Hong Kong
- Sun Yat-Sen University


