2002
DOI: 10.1007/s101470200022
|View full text |Cite
|
Sign up to set email alerts
|

Immunohistochemical demonstration of apoptosis-regulated proteins, Bcl-2 and Bax, in resected non-small-cell lung cancers

Abstract: Bcl-2 overexpression was significantly associated with SCC. Spontaneous apoptosis was significantly associated with SCC and with negative nodal metastasis. Apoptosis-regulated proteins, Bcl-2 and Bax, and AI lack significant associations with each other and prognostic values in patients with resected NSCLC.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

6
9
1

Year Published

2004
2004
2010
2010

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 26 publications
(16 citation statements)
references
References 23 publications
6
9
1
Order By: Relevance
“…In agreement with the aforementioned cDNA study, the almost identical percentages of molecular alterations reported herein support the hypothesis that lung cancer detected in a screening program has a similar malignant potential than conventionally, nonscreen-detected cancer. Furthermore, all the data from both series are concordant with the published literature on resectable non -small cell lung cancer in relation to cell cycle -related proteins (18,21,23,24,33,(40)(41)(42), apoptosis regulators (26,43,44), invasive and angiogenic markers (26,27), RNA processing molecules (28,29), and genetic aberrations (15,38).…”
Section: Discussionsupporting
confidence: 84%
See 1 more Smart Citation
“…In agreement with the aforementioned cDNA study, the almost identical percentages of molecular alterations reported herein support the hypothesis that lung cancer detected in a screening program has a similar malignant potential than conventionally, nonscreen-detected cancer. Furthermore, all the data from both series are concordant with the published literature on resectable non -small cell lung cancer in relation to cell cycle -related proteins (18,21,23,24,33,(40)(41)(42), apoptosis regulators (26,43,44), invasive and angiogenic markers (26,27), RNA processing molecules (28,29), and genetic aberrations (15,38).…”
Section: Discussionsupporting
confidence: 84%
“…Thus, high levels of Ki-67 (18,19,40), loss of p16 (21), accumulation of p53 (45,46), cyclin E overexpression (40), and Bcl-2 expression (26,43,44,47) were observed more commonly in squamous cell carcinomas than in adenocarcinomas. However, p21 loss was observed more frequently in adenocarcinomas than in squamous cell carcinomas.…”
Section: Discussionmentioning
confidence: 98%
“…AI was defined as an amount of TUNEL positive cells per 1000 tumor cells, concordant with previously published methods [18,21,[23][24][25][26] and criteria [11,18,21,[23][24][25][26]. In the enlarged study group the mean and median AI remained similar to our previous study (12 vs. 14 and 8 vs. 9, respectively) [11], and within the range demonstrated by other authors (the mean AI range was 11-23, the median AI range was [8][9][10][11][12][13][14][15] [18,20,21,23,[26][27][28]. Similar to other authors [18,20,21], a larger number of cases allowed us to divide our group of patients into four subgroups, based on 25th, 50th and 75th percentile of AI.…”
Section: Discussionsupporting
confidence: 79%
“…We did not find any correlation between AI and patient characteristics. In other NSCLC series higher AI was associated with squamous (Hanaoka et al 2002) or adenous lung cancer subtype (To¨rma¨nen et al 1995). Tanaka et al (2002) reported that the highest AI was more common in moderate-or poor-differentiated than in well-differentiated NSCLC cases, whereas in lymphomas, breast, endometrial or thyroid carcinomas, higher apoptosis was associated with the less differentiated tumors (revied by Soini et al 1998).…”
Section: Discussionmentioning
confidence: 96%