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DNA Ploidy and Proliferative Activity in bcl-2 Expressed Non-small Cell lung Cancer
OBJECTIVES: The expressions of bcl-2 have been reported recently in non-small cell lung carcinoma (NSCLC). As oncogensis is believed to involve a number of genetic alterations, there can be differences in DNA ploidy or proliferative activity even in bcl-2 positive cases according to the superimposed...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association of Internal Medicine
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532009/ https://www.ncbi.nlm.nih.gov/pubmed/8854645 http://dx.doi.org/10.3904/kjim.1996.11.2.101 |
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author | Kim, Young-Chul Park, Kyung-Ok Kim, Hyeoung-Joon Choi, In-Seon Park, Chang-Soo Juhng, Sang-Woo |
author_facet | Kim, Young-Chul Park, Kyung-Ok Kim, Hyeoung-Joon Choi, In-Seon Park, Chang-Soo Juhng, Sang-Woo |
author_sort | Kim, Young-Chul |
collection | PubMed |
description | OBJECTIVES: The expressions of bcl-2 have been reported recently in non-small cell lung carcinoma (NSCLC). As oncogensis is believed to involve a number of genetic alterations, there can be differences in DNA ploidy or proliferative activity even in bcl-2 positive cases according to the superimposed genetic events. SUBJECTS AND METHODS: On the assumption that we might further discern the biologic behavior of bcl-2 positive NSCLC according to the status of DNA ploidy and proliferative activity, we conducted a study for bcl-2 expression with immunohistochemical staining and DNA analysis on 52 surgical specimens of NSCLC. RESULTS: The bcl-2 was positive in 52% (27/52) of specimens, According to the status of bcl-2 expression, there were no significant differences in tumor stages, performance status score and survival time. Among bcl-2 positive NSCLC, aneuploidy and high proliferative activity were noted in 40% and 44%, respectively. In cases with squamous cell carcinoma (SQC), the proportion of aneuploidy was significantly higher in bcl-2 positive group compared to bcl-2 negative group (p<0.01), which could not be explained with the sole effect of bcl-2. In bcl-2 positive NSCLC, there was no significant survival difference by the status of DNA analysis results. With a Coxproportional hazard model, only T stage was an independent prognostic factor. CONCLUSION: In bcl-2 expressed NSCLC, proliferative activity and DNA ploidy were not homogeneous, suggesting other genetic alterations. This may explain our results which showed no differences in survival according to the status of the bcl-2 expression. |
format | Online Article Text |
id | pubmed-4532009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-45320092015-10-02 DNA Ploidy and Proliferative Activity in bcl-2 Expressed Non-small Cell lung Cancer Kim, Young-Chul Park, Kyung-Ok Kim, Hyeoung-Joon Choi, In-Seon Park, Chang-Soo Juhng, Sang-Woo Korean J Intern Med Original Article OBJECTIVES: The expressions of bcl-2 have been reported recently in non-small cell lung carcinoma (NSCLC). As oncogensis is believed to involve a number of genetic alterations, there can be differences in DNA ploidy or proliferative activity even in bcl-2 positive cases according to the superimposed genetic events. SUBJECTS AND METHODS: On the assumption that we might further discern the biologic behavior of bcl-2 positive NSCLC according to the status of DNA ploidy and proliferative activity, we conducted a study for bcl-2 expression with immunohistochemical staining and DNA analysis on 52 surgical specimens of NSCLC. RESULTS: The bcl-2 was positive in 52% (27/52) of specimens, According to the status of bcl-2 expression, there were no significant differences in tumor stages, performance status score and survival time. Among bcl-2 positive NSCLC, aneuploidy and high proliferative activity were noted in 40% and 44%, respectively. In cases with squamous cell carcinoma (SQC), the proportion of aneuploidy was significantly higher in bcl-2 positive group compared to bcl-2 negative group (p<0.01), which could not be explained with the sole effect of bcl-2. In bcl-2 positive NSCLC, there was no significant survival difference by the status of DNA analysis results. With a Coxproportional hazard model, only T stage was an independent prognostic factor. CONCLUSION: In bcl-2 expressed NSCLC, proliferative activity and DNA ploidy were not homogeneous, suggesting other genetic alterations. This may explain our results which showed no differences in survival according to the status of the bcl-2 expression. Korean Association of Internal Medicine 1996-06 /pmc/articles/PMC4532009/ /pubmed/8854645 http://dx.doi.org/10.3904/kjim.1996.11.2.101 Text en Copyright © 1996 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Young-Chul Park, Kyung-Ok Kim, Hyeoung-Joon Choi, In-Seon Park, Chang-Soo Juhng, Sang-Woo DNA Ploidy and Proliferative Activity in bcl-2 Expressed Non-small Cell lung Cancer |
title | DNA Ploidy and Proliferative Activity in bcl-2 Expressed Non-small Cell lung Cancer |
title_full | DNA Ploidy and Proliferative Activity in bcl-2 Expressed Non-small Cell lung Cancer |
title_fullStr | DNA Ploidy and Proliferative Activity in bcl-2 Expressed Non-small Cell lung Cancer |
title_full_unstemmed | DNA Ploidy and Proliferative Activity in bcl-2 Expressed Non-small Cell lung Cancer |
title_short | DNA Ploidy and Proliferative Activity in bcl-2 Expressed Non-small Cell lung Cancer |
title_sort | dna ploidy and proliferative activity in bcl-2 expressed non-small cell lung cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532009/ https://www.ncbi.nlm.nih.gov/pubmed/8854645 http://dx.doi.org/10.3904/kjim.1996.11.2.101 |
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