## BACKGROUND. Radiotherapy is used in the treatment of laryngeal carcinoma. The search for biologic parameters that could be used to identify patients who will respond to radiotherapy is crucial. The aim of this study was to determine whether the Ki-67 and p53 indices and the pretreatment apoptot
Expression of apoptosis-related proteins, p53, and DNA fragmentation in sarcomas of the pulmonary artery
✍ Scribed by Andreas Gaumann; Dominique S. Tews; Eckhard Mayer; Manfred Dahm; Peter K. Petrow; Mike Otto; C. James Kirkpatrick; Jörg Kriegsmann
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 478 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
✦ Synopsis
Background:
Apoptosis is a common feature in a variety of pathologic conditions. induction of apoptosis through apoptotic stimuli such as, chemotherapy or radiation, presents new insights into tumor biology and therapy. in particular, members of the bcl-2 family as well as the fas system are known to be involved in the regulation of apoptosis in different tumor entities.
Methods:
In the current study, the expression of the apoptosis-related molecules p53, bax, bcl-2, fas (cd95), fas-ligand and perforin was examined in 7 patients with a sarcoma of the pulmonary artery. furthermore, the tunel-method for the detection of apoptotic cells was applied as well as sequencing of the p53 gene.
Results:
In the tunel assay, approximately 10% of the sarcoma cells displayed dna fragmentation. in addition, bax was expressed in tumor cells. accumulation of p53 was evident in 4 of 7 patients (pab 240 antibody), and 2 of them were positive for the pab 1801 antibody. only 1 case had a point mutation in exon 5 of the p53 sequence. a few tumor cells showed a double labeling of bax and p53. bcl-2 could be detected only in tumor-associated lymphocytes. finally, several lymphocytes could be stained with perforin, but none of the specimens showed a reactivity for fas or fas-ligand.
Conclusion:
The expression of bax indicated a possible role of this molecule in programmed cell death in pulmonary sarcomas. the limited coexpression of bax and p53 suggested that induction of bax can occur independently of p53. the detection of perforin in lymphocytes suggested a possible role for this molecule in apoptosis of the sarcoma cells. in contrast, the fas system did not seem to play an essential role in sarcomas of the great vessels.
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