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DOI: 10.1055/s-1999-9040
Pathogenesis of Malignant Pleural Effusions and Talc Pleurodesis[1]
Publication History
Publication Date:
31 December 1999 (online)
In this review I hope to cover two critical areas, namely the mechanism of formation of malignant pleural effusions and the treatment of malignant pleural effusions via pleurodesis. The pathogenesis of malignant pleural effusions involves several steps. These allow the malignant cell to separate from the primary tumor, dock onto the area of the metastatic site, transmigrate through the pleural membrane and initiate autocrine proliferation. The role of several factors including integrins and hyaluronan will be described. I will use the role of the glycosaminoglycan, hyaluronan, and its interaction with the CD44 receptor to illustrate the mechanisms of metastatic tumor formation on the pleural surface.
Since talc pleurodesis remains the mainstay of treatment for malignant pleural effusions, this review will discuss the inflammatory responses induced by talc and the mechanisms of talc induced fibrosis. The concept that the normal mesothelium plays a critical role in the development of pleural fibrosis will be introduced. The possibility that talc may serve other functions besides the induction of pleural fibrosis will be discussed.
1 Herrn Prof. Dr. R. Loddenkemper, Berlin, zum 60. Geburtstag gewidmet
Literature
- 1 Jiang W. In vitro models of cancer invasion and metastasis: recent developments. Eur J Surg Oncol. 1994; 20 493-499
- 2 Zetter B. Adhesion molecules in tumor metastasis. Semin Cancer Biol. 1993; 4 219-229
- 3 Sneath R J S, Managham D C. The normal structure and function of CD44 and its role in neoplasia. J Clin Pathol Mol Pathol. 1998; 51 191-200
- 4 Koukoulis G K, Patriarca C, Gould V E. Adhesion molecules and tumor metastasis. Human Pathol. 1998; 889-891
- 5 Trochon V, Mabilat C, Bertrand P et al. Evidence of involvement of CD44 in endothelial cell proliferation, migration and angiogenesis in vitro. Int J Cancer. 1996; 66 664-668
- 6 Bourguignon L, Lokeshwar V, Chen X et al. Hyaluronic acid induced lymphocyte signal transduction and HA receptor (GP85/CD44)-cytoskeleton interaction. J Immunol. 1993; 1551 6634-6644
-
7 Menzel E J, Farr C.
Hyaluronidase and its substrate hyaluronan: biochemistry, biological activities and therapeutic uses . Cancer Letters 1998: 3-11 - 8 Johnson J P. Cell adhesion molecules of the immunoglobin supergene family and their role in malignant transformation and progression to metastatic disease. Cancer Metastasis Rev. 1991; 10 11-12
- 9 Bukholm I K, Nesland J M, Karesen R et al. E-Cadherin and α, β- and γ-catenin protein expression in relation to metastasis in human breast carcinoma. J Pathol. 1998; 185 262-266
- 10 Underhill C. CD44: the hyaluronan receptor. J Cell Sci. 1992; 103 293-298
- 11 Ponta H, Wainwright D, Herrlich P. Molecules in focus: The CD44 protein family. Int J Biochem Cell Biol. 1998; 30 299-305
- 12 Hott J W, Godbey S W, Antony V B. The role of the mesothelial cell in pleural metastasis; Inhibition of breast carcinoma cell adherence to pleural cells by hyaluronidase. FASEB J. 1992; 6 (5) 1919
- 13 Hott J W, Godbey S W, Antony V B. The role of the mesothelial cell in pleural metastasis: Breast carcinoma cell adherence to pleural mesothelial cells by a mechanism involving hyaluronate and CD44. Am Rev Respir Dis. 1993; 147 (4) A794
- 14 Hott J W, Yu L, Godbey S W, Holm K A, Antony V B. The role of the mesothelial cell in pleural metastasis; breast carcinoma cell proliferation in response to a pleural mesothelial cell derived growth factor. Am J Respir Crit Care Med. 1996; 153 (4) A44
- 15 Seiter S, Arch R, Reber S, Komitowski D, Ponta M, Ponta H, Matzku S, Zoller M. Prevention of tumor metastasis formation by anti-variant CD44. J Exp Med. 1993; 177 443-455
- 16 Naor D, Sionov R V, Shalom D I. CD44: structure, function and association with the metastatic process. Adv Can Res. 1997; 71 241-319
- 17 Hott J W, Yu L, Antony V B. Mechanisms of pleural metastasis: MCF-7 breast adenocarcinoma cell haptotaxis to hyaluronic acid. Am J Resp Crit Care Med. 1997; 155 A180
- 18 Bennett K L, Jackson D G, Simon J C, Tanczos E, Modrell R, Modrell B, Stamenkovic I, Plaowman G, Aruffo A. CD44 isoforms containing exon v3 are responsible for the presentation of heparin-binding growth factor. J Cell Biol. 1995; 128 687-698
- 19 Zawadzki V, Perschl A, Rosel M, Hekele A, Zoller M. Blockade of metastasis formation by CD44-receptor globulin. Int J Cancer. 1998; 75 919-924
- 20 Ozer E, Canda T, Kurtoolu B. The role of angiogensis, laminin and CD44 expression in metastatic behavior of early-stage low-grade invasive breast carcinomas. Cancer Letters. 1997; 122 119-123
- 21 Stetler-Stevenson W G. Matrix metalloproteinases in angiogenesis: a moving target for therapeutic intervention. Clin Invest. 1999; 103, #9 1237-1241
- 22 Eliceiri B P, Cheresh D A. The role of αv integrins during angiogenesis: insights into potential mechanisms of action and clinical development. Clin Invest. 1999; 103, #9 1227-1230
- 23 Isner J M, Asahara T. Angiogenesis and vasculogenesis as therapeutic strategies for postnatal neovascularization. The Journal of Clinical Investigation. 1999; 103, #9 1231-1236
- 24 Hott J W, Yu L, Antony V B. Role of VEGF in the formation of malignant pleural effusions. Am J Respir Crit Care Med. 1999; 159 A212
- 25 Galffy G, Mohammed K A, Ward M J, Dowling P A, Antony V B. Interleukin 8 - An autocrine growth factor for malignant mesothelioma. Am Cancer Res. 1999; 59 367-371
- 26 Bethune N. Pleural poudrage: a new technique for the deliberate production of pleural adhesions as a preliminary to lobectomy. J Thorac Surg. 1935; 4 251-261
- 27 Loddenkemper R. Thoracoscopy - state of the art. Eur Respir J. 1998; 11 213-221
- 28 Rodriquez-Panadero F, Antony V B. Pleurodesis: state of the art. Eur Respir J. 1997; 10 1648-1654
- 29 Walker-Renard P B, Vaughan L M, Sahn S A. Chemical pleurodesis for malignant pleural effusions. Ann Int Med. 1994; 120 56-64
- 30 Kennedy L, Vaughan L M, Steed L L, Sahn S A. Sterilization of talc for pleurodesis: available techniques, efficacy and cost analysis. Chest. 1995; 107/4 1032-1034
- 31 Heuvel M M, Smith H J M, Barbierato S B, Havenith C EG, Beelen R HJ, Postmus P E. Talc-induced inflammation in the pleural cavity. Eur Respir J. 1998; 12 1419-1423
- 32 Rodriguez-Panadero F, Segado A, Martin Juan J, Ayerbe R, Torres Garcia I, Castillo J. Failure of talc pleurodesis is associated with increased pleural fibrinolysis. Am J Respir Crit Care Med . 1995; 785-790
- 33 Nasreen N, Hartman D L, Mohammed K A, Antony V B. Talc-induced expression of C-C and C-X-C chemokines and intercellular adhesion molecule-1 in mesothelial cells. Am J Respir Crit Care Med. 1998; 158 971-978
- 34 Antony V B, Kamal M A, Godbey S, Loddenkemper F W. Talc induced pleurodesis: Role of basic fibroblast growth factor (bFGF). Eur Respir J. 1997; 10 403S
- 35 Colt H G, Russack V, Chiu Y, Konopka R G, Chiles P G, Pedersen C A, Kapelanski D. A comparison of thoracoscopic talc insufflation, slurry and mechanical abrasion pleurodesis. Chest. 1997; 111/2 442-448
- 36 Nasreen N, Mohammed K A, Dowling P A, Ward M J, Galffy G, Antony V B. Talc induces apoptosis in human malignant mesothelioma cells in vitro. Am J Respir Crit Care Med. 1998; 157 (3) A63
1 Herrn Prof. Dr. R. Loddenkemper, Berlin, zum 60. Geburtstag gewidmet
MD Veena B. Antony
Professor of Medicine and Pediatrics Indiana University School of Medicine Chief, Pulmonary and Critical Care Medicine RL Roudebush VA Medical Center
1481 West 10th Street
Indianapolis, IN 46202
USA
Email: vantony@iupui-edu