Postmenopausal structural and molecular rearrangements in the polyps and adjacent endometrium: processes of proliferation, neoangiogenesis, aging, and apoptosis


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Objective. To morphologically examine the processes of growth, neoangiogenesis, aging, and apoptosis in the polyps and their adjacent endometrium in postmenopausal women. Subject and methods. Forty-six women were examined. Group 1 included 11 patients with adenomatous polyps (AP); Group 2 comprised 17patients with fibroglandular polyps (FGP); Group 3 consisted of 18 patients with the atrophic endometrium and no evidence of polyps (a control group). The expression of the markers of Ki-67, VEGF, ApoCas, PTEN, and p16 INK4a was assessed in the epithelial and stromal cells of a polyp and its adjacent endometrium and in those of the control endometrium. Results. The AP epithelium has high proliferation, low apoptosis, and, on occasion, changes characteristic of malignant cell transformation (PTEN loss, p16 INK4a and Ki-67 coexpression). There is a significant difference between the surrounding AP and GFP endometrium that in turn distinct from the control endometrium. Conclusion. AP and GGP have different mechanisms of pathogenesis and differ not only in their morphological structure, but also in the expression of the markers of growth, neoangiogenesis, aging, and apoptosis in their stromal and epithelial components. The findings should be recommended to improve a differential approach to their treatment and to decide on the volume of endometrial destruction in this pathology.

Full Text

Restricted Access

About the authors

E. A Kogan

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: e_kogan@oparina4.ru
MD. Prof. I Pathology Department

Sh. N Sattarov

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: docshuhrat@yahoo.com
postgraduate

S. E Sarkisov

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: 734l497@mail.ru
MD, professor, Innovational Department of minimally invasive technologies in gynecology

N. M Faizullina

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: n_faizullina@oparina4.ru
Senior Research Fellow, I Pathology Department

References

  1. Бреусенко В.Г., Голова Ю.А., Каппушева Л.М., Мишиева О.И., Кирикова Ю.М., Цечоева Т.С. Современные подходы в лечении пролиферативных процессов эндометрия в постменопаузе. В кн. : Прилепская В.Н., ред. Клиническая гинекология. М.: МЕДпресс-информ; 2007: 315-23.
  2. Хитрых О.В. Отдаленные результаты и оптимизация тактики лечения полипов эндометрия в постменопаузе: Автореф. дис.. канд. мед. наук. М.; 2009.
  3. Antunes A.Jr., Costa-Parva L., Arthuso M., Costa J.V., Pinto-Neto A.M. Endometrial polyps in pre- and postmenopausal women: factors associated with malignancy. Maturitas. 2007; 57: 415-21.
  4. Newell S., Overton C. Postmenopausal bleeding should be referred urgently. Practitioner. 2012; 256(1749):13-5, 2.
  5. American Association of Gynecologic Laparoscopists. AAGL practice report: practice guidelines for the diagnosis and management of endometrial polyps. J. Minim. Invasive Gynecol. 2012; 19(1): 3-10.
  6. Costa-Parva L., Godoy C.E.Jr., Antunes AJr., Caseiro J.D., Arthuso M., Pinto-Neto A.M. Risk of malignancy in endometrial polyps in premenopausal and postmenopausal women according to clinicopathologic characteristics. Menopause. 2011; 18(12): 1278-82.
  7. Fletcher J.A., Pinkus J.L., Lage J.M., Morton C.C., Pinkus G.S. Clonal 6p21 rearrangement is restricted to the mesenchymal component of an endometrial polyp. Genes Chromosomes Cancer. 1992; 5(3): 260-3.
  8. Dal Cin P., Vanni R., Marras S., Moerman P., Kools P., Andria M. et al. Four cytogenetic subgroups can be identified in endometrial polyps. Cancer Res. 1995; 55(7): 1565-8.
  9. Erdemoglu E., Güney M., Karahan N., Mungan T. Expression of cyclooxy-genase-2, matrix metalloproteinase-2 and matrix metalloproteinase-9 in premenopausal and postmenopausal endometrial polyps. Maturitas. 2008; 59(3): 268-74.
  10. Taylor L.J., Jackson T.L., Reid J.G., Duffy S.R. The differential expression of oestrogen receptors, progesterone receptors, Bcl-2 and Ki67 in endometrial polyps. Br. J. Obstet. Gynaecol. 2003; 110: 794-8.
  11. Maia H.Jr., Maltez A., Athayde C., Coutinho E.M. c-erbB2 over-expression in endometrial hyperplasia induced by estrogens. Maturitas. 2002; 43(1): 41-7.
  12. Maia H.Jr., Maltez A., Studart E., Athayde C., Coutinho E.M. Ki-67, Bcl-2 and p53 expression in endometrial polyps and in the normal endometrium during the menstrual cycle. Br. J. Obstet. Gynaecol. 2004; 111(11): 1242-7.
  13. Risberg B., Karlsson K., Abeler V., Lagrelius A., Davidson B., Karlsson M. Dissociated expression of Bcl-2 and Ki67 in endometrial lesions: diagnostic and histogenetic implications. Int. J. Gynecol. Pathol. 2002; 21: 155-60.
  14. Antunes A.Jr.,Andrade L.A., Pinto G.A., Leao R., Pinto-Neto A.M., Costa-Paiva L. Is the immunohistochemical expression of proliferation (Ki-67) and apoptosis (Bcl-2) markers and cyclooxigenase-2 (COX-2) related to carcinogenesis in postmenopausal endometrial polyps? Anal. Quant. Cytol. Histol. 2012; 34(5): 264-72.
  15. Савельева Г.М., Бреусенко В.Г., Каппушева Л.М. Гестероскопия: атлас и руководство. М.: ГЭОТАР-Медиа; 2013. 248 с.
  16. Lapak K.M., Burd C.E. The molecular balancing act of p16INK4a in cancer and aging. Mol. Cancer Res. 2013; Oct 17.
  17. Janzen V, Forkert R, Fleming H.E., Saito Y., Waring M.T., Dombkowski D.M. et al. Stem-cell ageing modified by the cyclin-dependent kinase inhibitor p16INK4a. Nature. 2006; 443(7110): 421-6.
  18. Simboeck E., Di Croce L. p16INK4a in cellular senescence. Aging (Albany NY). 2013; 5(8): 590-1.
  19. Wentzensen N., Schwartz L., Zuna R.E., Smith K., Mathews C., Gold M.A. et al. Performance of p16/Ki-67 immunostaining to detect cervical cancer precursors in a colposcopy referral population. Clin. Cancer Res. 2012; 18(15): 4154-62.
  20. Kurman R.J., ed. Blaustein’s pathology of the female genital tract. 5th ed. New York: Springer-Verlag; 2002: 421-66.
  21. Erkanli S., Kayaselcuk F., Kuscu E., Bagis T., Bolat F., Haberal A., Demirhan B. Expression of survivin, PTEN and p27 in normal, hyperplastic, and carcinomatous endometrium. Int. J. Gynecol. Cancer. 2006; 16(3): 1412-8.
  22. Kapucuoglu N., Aktepe F., Kaya H., Bircan S., Karahan N., Ciris M. Immunohistochemical expression of PTEN in normal, hyperplastic and malignant endometrium and its correlation with hormone receptors, bcl-2, bax, and apoptotic index. Pathol. Res. Pract. 2007; 203(3): 153-62.
  23. Копнин Б.П. Опухолевые супрессоры и мутаторные гены. В кн.: Заридзе Д.Г., ред. Канцерогенез. М.: Научный мир; 2000: 75-96.
  24. Метельская М.А., Рогов Ю.И. Экспрессия предикторов неоплазий PTEN и PAX-2 в эндометрии. Здравоохранение. 2013; 1: 26-31.
  25. Бантыш Б.Б., Пауков В.С., Коган Е.А. Иммуноморфологические особенности эпителиально-стромальных взаимоотношений при гиперплазии и раке эндометрия. Архив патологии. 2012; 74(3): 22-5.
  26. Xuebing P., TinChiu L., Enlan X., Jing L., Xiaowu H. Is endometrial polyp formation associated with increased expression of vascular endothelial growth factor and transforming growth factor-beta1? Eur. J. Obstet. Gynecol. Reprod. Biol. 2011; 159(1): 198-203.

Supplementary files

Supplementary Files
Action
1. JATS XML

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies