CD97 expression level and its effect on cell adhesion in Preeclampsia

被引:4
作者
Atigan, Ayhan [1 ]
Tan, Semih [2 ]
Cetin, Hulya [2 ]
Guler, Omer Tolga [3 ]
Ozdamar, Saim [2 ]
Karakaya, Yeliz Arman [4 ]
机构
[1] Karabuk Univ, Fac Med, Sch Med, Dept Obstet & Gynecol, Karabuk, Turkey
[2] Pamukkale Univ, Fac Med, Dept Histol & Embryol, Denizli, Turkey
[3] Pamukkale Univ, Fac Med, Dept Obstet & Gynecol, Denizli, Turkey
[4] Pamukkale Univ, Fac Med, Dept Pathol, Denizli, Turkey
关键词
Preeclampsia; Cadherins; CD97; E-cadherin; N-cadherin; Integrin beta-4; E-CADHERIN; INTEGRIN ALPHA-6-BETA-4; INVASION; RECEPTOR; ANGIOGENESIS; TROPHOBLASTS; INCREASE; EGF-TM7;
D O I
10.1186/s12884-022-05280-z
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: Cellular interactions and cell adhesion underlie preeclampsia (PE). The aim of the current study is to investigate the role of cell adhesion molecules such as CD97, neural (N)-cadherin, epithelial (E) -cadherin and integrin beta-4 in PE. Methods: This prospective study included 20 pregnant women with PE and a control group of 16 healthy pregnant women who were matched for age, gestational age, gravida and parity. Standard blood tests and placental cell adhesion molecule immunohistochemical staining were examined. Results: The creatinine, uric acid and lactate dehydrogenase (LDH) levels from standard blood tests were found to be statistically higher in the PE group (p = 0.002, p = 0.000, p = 0.001; respectively). In the PE group, the CD97 maternal serum level was statistically significantly lower, as was its immunohistochemical expression in placental sections (p = 0.028, p = 0.000; respectively). The E-cadherin expression score was statistically higher in the PE group compared to the control group (3,65 +/- 1,84 vs 2,06 +/- 1,76 respectively; p = 0.003). The N-cadherin expression score was statistically lower in the PE group compared to the control group (1,50 +/- 0,82 vs 2,43 +/- 1,59 respectively; p = 0.049). Integrin beta-4 was not statistically different between groups. Conclusions: Cellular interaction may be responsible for PE as in cancer. A balance in intercellular communication, as researched in cancer therapy, may offer the solution in PE.
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页数:8
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共 42 条
[1]   Structural and functional characterization of a novel T cell receptor co-regulatory protein complex, CD97-CD55 [J].
Abbott, Rachel J. M. ;
Spendlove, Ian ;
Roversi, Pietro ;
Fitzgibbon, Hannah ;
Knott, Vroni ;
Teriete, Peter ;
McDonnell, James M. ;
Handford, Penny A. ;
Lea, Susan M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (30) :22023-22032
[2]   Gestational Hypertension and Preeclampsia [J].
Espinoza, Jimmy ;
Vidaeff, Alex ;
Pettker, Christian M. ;
Simhan, Hyagriv .
OBSTETRICS AND GYNECOLOGY, 2020, 135 (06) :E237-E260
[3]   CAN PLACENTAL HISTOPATHOLOGICAL LESIONS BE A GUIDE TO MATERNAL AND NEONATAL OUTCOMES IN PATIENTS WITH PREECLAMPSIA? [J].
Atigan, Ayhan ;
Kilic, Derya ;
Guler, Tolga ;
Karakaya, Yeliz Arman .
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, 2022, 85 (03) :425-432
[4]   The e-cadherin repressor snail plays a role in tumor progression of Endometrioid adenocarcinomas [J].
Blechschmidt, Kareen ;
Kremmer, Elisabeth ;
Hollweck, Regina ;
Mylonas, Ioannis ;
Hoefler, Heinz ;
Kremer, Marcus ;
Becker, Karl-Friedrich .
DIAGNOSTIC MOLECULAR PATHOLOGY, 2007, 16 (04) :222-228
[5]   E-cadherin in the assessment of aberrant placental cytotrophoblast turnover in pregnancies complicated by pre-eclampsia [J].
Brown, LM ;
Lacey, HA ;
Baker, PN ;
Crocker, IP .
HISTOCHEMISTRY AND CELL BIOLOGY, 2005, 124 (06) :499-506
[6]   Down-regulation of the transcription factor snail in the placentas of patients with preeclampsia and in a rat model of preeclampsia [J].
Fedorova, Larisa ;
Gatto-Weis, Cara ;
Smaili, Sleiman ;
Khurshid, Nauman ;
Shapiro, Joseph I. ;
Malhotra, Deepak ;
Horrigan, Terrence .
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2012, 10
[7]   Localization of E-cadherin in villous, extravillous and vascular trophoblasts during intrauterine, ectopic and molar pregnancy [J].
Floridon, C ;
Nielsen, O ;
Holund, B ;
Sunde, L ;
Westergaard, JG ;
Thomsen, SG ;
Teisner, B .
MOLECULAR HUMAN REPRODUCTION, 2000, 6 (10) :943-950
[8]   Positional control of cell fate through joint integrin/receptor protein kinase signaling [J].
Giancotti, FG ;
Tarone, G .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2003, 19 :173-206
[9]   Cell Signaling Pathways Involved During Invasion and Syncytialization of Trophoblast Cells [J].
Gupta, Satish Kumar ;
Malhotra, Sudha Saryu ;
Malik, Ankita ;
Verma, Sonam ;
Chaudhary, Piyush .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2016, 75 (03) :361-371
[10]   International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G Protein-Coupled Receptors [J].
Hamann, Joerg ;
Aust, Gabriela ;
Arac, Demet ;
Engel, Felix B. ;
Formstone, Caroline ;
Fredriksson, Robert ;
Hall, Randy A. ;
Harty, Breanne L. ;
Kirchhoff, Christiane ;
Knapp, Barbara ;
Krishnan, Arunkumar ;
Liebscher, Ines ;
Lin, Hsi-Hsien ;
Martinelli, David C. ;
Monk, Kelly R. ;
Peeters, Miriam C. ;
Piao, Xianhua ;
Proemel, Simone ;
Schoeneberg, Torsten ;
Schwartz, Thue W. ;
Singer, Kathleen ;
Stacey, Martin ;
Ushkaryov, Yuri A. ;
Vallon, Mario ;
Wolfrum, Uwe ;
Wright, Mathew W. ;
Xu, Lei ;
Langenhan, Tobias ;
Schoeith, Helgi B. .
PHARMACOLOGICAL REVIEWS, 2015, 67 (02) :338-367