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Low expression of Bax predicts poor prognosis in resected non-small cell lung cancer patients with non-squamous histology.
DC Field | Value | Language |
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dc.contributor.author | Jeong, SH | - |
dc.contributor.author | Lee, HW | - |
dc.contributor.author | Han, JH | - |
dc.contributor.author | Kang, SY | - |
dc.contributor.author | Choi, JH | - |
dc.contributor.author | Jung, YM | - |
dc.contributor.author | Choi, H | - |
dc.contributor.author | Oh, YT | - |
dc.contributor.author | Park, KJ | - |
dc.contributor.author | Hwang, SC | - |
dc.contributor.author | Sheen, SS | - |
dc.contributor.author | Oh, YJ | - |
dc.contributor.author | Kim, JH | - |
dc.contributor.author | Lim, HY | - |
dc.date.accessioned | 2010-12-23T01:55:37Z | - |
dc.date.available | 2010-12-23T01:55:37Z | - |
dc.date.issued | 2008 | - |
dc.identifier.issn | 0368-2811 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/775 | - |
dc.description.abstract | OBJECTIVE: The present study evaluated the prognostic significance of apoptosis-related proteins p53, Bax and galectin-3 in patients with non-small cell lung cancer (NSCLC) treated with surgical resection.
METHODS: We investigated the expression of these proteins and their association with clinicopathologic characteristics including disease-free survival (DFS) and overall survival (OS) in 205 NSCLC patients who underwent surgical resection (Stage I, 97; II, 46; IIIA, 45; IIIB, 17) using immunohistochemistry. Eighty-eight patients (43%) received adjuvant treatment (chemotherapy: 8, radiotherapy: 24, both: 56). RESULTS: High expressions of Bax, p53 and galectin-3 were observed in 48 (23%), 81 (40%) and 105 (51%) patients, respectively. Low expression of Bax was significantly associated with male gender, squamous cell histology and low expression of galectin-3. Five-year DFS and OS of total patients were 37 and 46%, respectively. High expressions of p53 and galectin-3 were not associated with poor DFS or OS, and no significant correlation existed between low expression of Bax and outcome of patients. However, in patients with non-squamous histology (108 patients), low expression of Bax was a significant independent predictor of poor DFS (P = 0.017) and OS (P = 0.037). In addition, in patients with Stage II or III disease, low expression of Bax significantly correlated with poor DFS (P = 0.004). It was also the most significant independent poor prognostic factor second only to a large primary tumor size in Stage II or III patients with non-squamous histology. CONCLUSIONS: Low expression of Bax was significantly associated with poor prognosis in resected NSCLC patients with non-squamous histology. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols | - |
dc.subject.MESH | Carboplatin | - |
dc.subject.MESH | Carcinoma, Non-Small-Cell Lung | - |
dc.subject.MESH | Carcinoma, Squamous Cell | - |
dc.subject.MESH | Chemotherapy, Adjuvant | - |
dc.subject.MESH | Combined Modality Therapy | - |
dc.subject.MESH | Deoxycytidine | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Galectin 3 | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Immunoenzyme Techniques | - |
dc.subject.MESH | Lung Neoplasms | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Radiotherapy Dosage | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Survival Rate | - |
dc.subject.MESH | Tissue Array Analysis | - |
dc.subject.MESH | Tumor Suppressor Protein p53 | - |
dc.subject.MESH | bcl-2-Associated X Protein | - |
dc.title | Low expression of Bax predicts poor prognosis in resected non-small cell lung cancer patients with non-squamous histology. | - |
dc.type | Article | - |
dc.identifier.pmid | 18772168 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565351/ | - |
dc.contributor.affiliatedAuthor | 정, 성현 | - |
dc.contributor.affiliatedAuthor | 이, 현우 | - |
dc.contributor.affiliatedAuthor | 한, 재호 | - |
dc.contributor.affiliatedAuthor | 강, 석윤 | - |
dc.contributor.affiliatedAuthor | 최, 진혁 | - |
dc.contributor.affiliatedAuthor | 최, 호 | - |
dc.contributor.affiliatedAuthor | 오, 영택 | - |
dc.contributor.affiliatedAuthor | 박, 광주 | - |
dc.contributor.affiliatedAuthor | 황, 성철 | - |
dc.contributor.affiliatedAuthor | 신, 승수 | - |
dc.contributor.affiliatedAuthor | 김, 장희 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1093/jjco/hyn089 | - |
dc.citation.title | Japanese journal of clinical oncology | - |
dc.citation.volume | 38 | - |
dc.citation.number | 10 | - |
dc.citation.date | 2008 | - |
dc.citation.startPage | 661 | - |
dc.citation.endPage | 669 | - |
dc.identifier.bibliographicCitation | Japanese journal of clinical oncology, 38(10). : 661-669, 2008 | - |
dc.identifier.eissn | 1465-3621 | - |
dc.relation.journalid | J003682811 | - |
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