Korean J Thorac Cardiovasc Surg.
2000 Jan;33(1):60-67.
Microsatellite Instability and p53 , k-ras c-myc Oncoprotein Expression in
Non-Small Cell Lung Carcinoma
- Affiliations
-
- 1Department of Thoracic and Cardiovascular Surgery, Surgery, Catholic University Medical college.
Abstract
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BACKGROUND: Microsatellites are short-tandem repeated uncleotide sequences present throughout
the human genome. Alterations of microsatellites have been termed microsatellite
instability(MI). It has been generally known that microsatellite instability detected in
hereditary non-polyposis colorectal cancer (HNPCC) reflects genetic instability that is
caused by impairments of DNA mismatch repair system regarding as a novel tumorigenic
mechanism. A number of studies reported that MI occurred at varying frequencies in non-small
cell lung carcinoma (NSCLC). However It has been unproven whether MI could be a useful market
of genetic instability and have a clinical significance in NSCLC.
MATERIAL AND METHOD: We have examined whether MI can be observed in thirty NCSLC using
polymerase chain reaction whether such alterations are associated with other molecular changes
such as p53, K-ras and c-myc oncoproteins expression detected by immunohistochemical stain,.
RESULT: MI(+) was observed in 16.6%(5/30) and MI(-) was 83.3% (25/30) Average age was
50+/-7.5 year-old in MI(+) group and 57+/-6.6 year-old in MI(-) group. Two year survival rate
in MI(=) group (20% 1/5) was worse than MI(-) group (64% 16/25) with a statistic difference.
(P=0.04) The positive rate of K-ras oncoprotein expression and simultaneous expression of 2
or 3 oncoproteins expression were higher in MI(+) group than MI(-) group with a statistic
difference(P=0.05, P=0.01)
CONCLUSIONS
From, these results the authors can conclude that MI is found in some NSCLC and
it may be a novel tumorigenic mechanism in some NSCLC. We also conclude that MI could be used
as another poor prognostic factor in NSCLS.