Abstract

Nine primary pulmonary carcinomas, one metastatic carcinoma, and two malignant pleural mesotheliomas have been analysed for the expression at the mRNA level of metalloproteinases (MPs) and tissue inhibitors of MPs (TIMPs). In situ hybridisation showed TIMP-1 and TIMP-2 transcripts predominantly over tumour stroma and gelatinases evenly distributed over both stromal and tumour cells. While both TIMP-1 and TIMP-2 were expressed in non-neoplastic lungs (NNL) as well as in carcinomas, stromelysin 3 (ST3), 92 kDa gelatinase and interstitial collagenase were expressed only by carcinomas. Expression of these MPs by carcinomas was independent of histologic type and such tumour features as fibrosis or necrosis. The consistent expression of ST3 by all of the carcinomas examined and absence of its expression in NNL indicates that ST3 production is likely associated with the malignant phenotype. However, since 92 kDa gelatinase and interstitial collagenase transcripts were found in some but not all tumour samples, their expression is not a uniform feature of pulmonary carcinomas. The possible prognostic significance of the expression of the latter two enzymes by carcinomas remains to be established.

Highlights

  • For some of the genes under study, striking differences in expression patterns between RNA isolated from carcinomas and non-neoplastic lungs (NNL) were observed

  • Transcripts corresponding to stromelysin 3 (ST3), 92 kDa gelatinase and interstitial collagenase were found only in tumour samples, but not in NNL

  • For ST3, RNA levels were low in all but two primary adenocarcinomas, where strong signals were obtained from samples from the pleural tumour aspect

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Summary

Objectives

The purpose of this study was to investigate the patterns of expression of major MPs and TIMPs in primary lung carcinomas

Methods
Results
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Conclusion
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