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Original Research

Open Access

Gains and losses of glycoprotein CD44 and secretory component expression in endometrial hyperplasia and neoplasia

  • D. Tamiolakis1
  • A. Kotini2
  • A. Cheva3
  • T. Jivannakis4
  • M. Lambropoulou1
  • M. Bobos1
  • S. Vavetsis1
  • N. Papadopoulos3,*,

1Department of Cytology, Regional Hospital of Alexandroupolis, Greece

2Department of Medical Physics, Democritus University of Thrace, Greece

3Department of Histology-Embryology, Democritus University of Thrace, Greece

4Department of Pathology, General Hospital of Drama, Greece

DOI: 10.12892/ejgo200205453 Vol.23,Issue 5,September 2002 pp.453-456

Published: 10 September 2002

*Corresponding Author(s): N. Papadopoulos E-mail:

Abstract

CD44 is an adhesion molecule, which binds hyaluronic acid and participates in a number of cell-cell interactions, including lymphocyte homing. The CD44 antigen is expressed on approximately 90% of lymphocytes, monocytes, granulocytes, and, in lower amounts on thymocytes, fibroblasts, and erythrocytes. Platelets lack CD44. In non-haematopoietic tissues, CD44 is widely distributed. The secretory component is isolated from human colostrum and is of help in more precise grading of endometrial carcinoma. In this study we examined CD44 and secretory component expression in adenomatous hyperplasia, atypical adenomatous hyperplasia and well-differentiated adenocarcinoma (cribriform pattern). The results showed decreased expression of CD44 and increased expression of secretory component as the lesion progressed to malignancy.

Keywords

Glygoprotein CD44; Endometrial hyperplasia; Endometrial neoplasia

Cite and Share

D. Tamiolakis,A. Kotini,A. Cheva,T. Jivannakis,M. Lambropoulou,M. Bobos,S. Vavetsis,N. Papadopoulos. Gains and losses of glycoprotein CD44 and secretory component expression in endometrial hyperplasia and neoplasia. European Journal of Gynaecological Oncology. 2002. 23(5);453-456.

References

[I] Horny H. P., Menke D. M., Kaiserling E.: "Neoplastic human tissue mast cells express the adhesion molecule CD44/HCAM". Virchows Arch., 1996, 429, 91.

[2] Fox S. B. et al., Cancer Res., 1994, 53, 4539.

[3] Haynes B. F., Liao X-P., Patton K. L.: "The transmembrane hyalurinate receptor (CD44): multiple functions, multiple forms". Cancer Cells, 1991, 3, 347.

[4] Ruiz P., Schwarzler C., Gunther T. U.: "CD44 isoforms during differentiation and development". BioEssays, 1994, 17, 17.

[5] Springer T. A.: "Traffic signals for lymphocyte recirculation and leukocyte emigration: the multi step paradigm". Cell, 1994, 76, 301.

[6] Thomas L.,B yers H. R., Vink J., Stamenkovic I.: "CD44 regulates tumor cell migration on hyaluronate-coated substrates". J. Cell BIOL., 1992, 118, 971.

[7] Wielega V. J. M., Heider K. H., Offerhaus J. A. et al.: "Expression of CD44 variant proteins in human colorectal cancer is related to tumor progression". Cancer Res., 1993, 53, 4754.

[8] Stauder R., Eisterer W., Thaler J., Gunthert U.: "CD44 variant isoforms in non-Hodgkin's lymphoma: A new independent prognostic factor". Blood, 1995, 10, 2885.

[9] Terpe H. J., Storkel S., Zimmer U. et al.: "Expression of CD44 isoforms in renal cell tumors: positive correlation to tumor progression". Am. J. Pathol., 1996, 148, 453.

[10] Fujita N., Yaegashi N., Ide et al.: "Expression of CD44 in normal versus tumor endometrial tissues: possible implications of reduced expression of CD44 in lymph-vascular space involvement of cancer cells". Cancer Res., 1994, 54, 3922.

[11] Hong R. L., Pu Y. S., Chu J. S., Lee W. J., Chen Y. C., Wu C. W.: "Correlation of expression of CD44 isoforms and E-cadherin with differentiation in human urothelial cell lines and transitional cell carcinoma". Cancer Lett., 1995, 89, 81.

[12] Salmi M., Gron-Virta K., Sointu P., Grenman R., Kalimo H., Jalkanen S.: "Regulated expression of exon v6 containing isoforms of CD44 in man: downregulation during malignant transformation of tumors of squamocellular origin". J. Cell Biol., 1993, 122, 431.

[13] Piffko J.,B ankfalvi A.,K lauke K. et al.: "Unaltered strong rmmunohistochemical expression of CD44-v6 and -v5 isoforms during development and progression of oral squamous cell carcinomas". J. Oral. Pathol. Med., 1996, 25, 502.

[14] Iida N.,B ourguignon L. Y.: "Coexpression of CD44 variant (cl0/ex l 4) and CD44s in human mammary epithelial cells promotes tumorigenesis". J. Cell Physiol., 1997, 171, 152.

[15] Bankfalvi A., Terpe H-J.,B reukelmann D.,B ier B., Rempe D., Pschadka G. et al.: "Gains and losses of CD44 expression during breast carcinogenesis and tumor progression". Histopathology, 1998, 33, 107.

[16] Nakopoulou L., Minaretzis D., Tsionou C., Mastrominas M.: "Value of immunohistochemical demonstration of several epithelial markers in hyperplastic and neoplastic endometrium". Gynecol. Oncol., 1990, 37 (3), 346.

[17] Welch W. R., Scully R. E.: "Precancerous lesions of the endometrium". Hum. Pathol., 1977, 8, 503.

[18] Kurman R. J., Kaminski P. F., Norris H. J.: "The behavior of endometrial hyperplasia: a long term study of "untreated" hyperplasia in 170 patients". Cancer, 1985, 56, 403.

[19] Frenczy A., Gelfand M.: "The biologic significance of cytologic atypia in progesterone-terated endometrial hyperplasia". Am. J. Obstet. Gynecol., 1989, 160, 126.

[20] Scully R. E., Poulson H., Sobin L.: "Histological typing of the female genital tract tumors".B erlin,S pringer-Verlag,1984.

[21] Tavassoli F., Kraus F. T.: "Endometrial lesions in uteri resected for atypical endometrial hyperplasia". Am. J. Clin. Pathol., 1978, 70, 770.

[22) Kurman R. J., Norris H. J.: "Evaluation of criteria for distinguishing atypical endometrial hyperplasia from well differentiated carcinoma". Cancer, 1982, 49, 2547.

[23] Chamlian D. L., Taylor H.B.: "Endometrial hyperplasia in young women". Obstet. Gynecol., 1970, 36, 659.

[24] Vellios F.: "Endometrial hyperplasias, precursors of endometrial carcinoma". Pathol. Annu., 1972, 7, 201.

[25] Hendrickson M. R., Ross J., Kempson R. L.: "Toward the development of morphologic criteria for well-differentiated adenocarcinoma of the endometrium". Am. J. Surg. Pathol., 1983, 7, 819.

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