Volume 22, Issue 6 (June 2024)                   IJRM 2024, 22(6): 495-506 | Back to browse issues page

Ethics code: IR.SKU.REC.1402.020


XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ahmadi K, Reiisi S, Habibi Z. Comparison of the gene expression profiles of endometrial and trophoblastic cells in women with recurrent miscarriage: A bioinformatics approach. IJRM 2024; 22 (6) :495-506
URL: http://ijrm.ir/article-1-3136-en.html
1- Department of Computer Sciences, Faculty of Mathematical Sciences, Shahrekord University, Shahrekord, Iran.
2- Department of Genetics, Faculty of Basic Sciences, Shahrekord University, Shahrekord, Iran. , s.reiisi@yahoo.com
3- Department of Women and Family Affairs, Chaharmahal and Bakhtiari Governorate, Shahrekord, Iran.
Abstract:   (288 Views)
Background: Recurrent miscarriage (RM) remains unsolved in > 50% of patients and causes physical and psychological problems in women without specific risk factors for miscarriage. For a successful pregnancy, acceptance of the endometrium and invasion of trophoblast cells into the endometrium is necessary.
Objective: This study aimed to use computational analysis to identify key genes and related pathways in endometrial and trophoblast cells derived from RM samples.
Materials and Methods: In this bioinformatics study, we explored the differential expression of genes in endometrial and trophoblast cells by analyzing the GSE165004 and GSE76862 datasets, respectively with the limma package in R software. Subsequently, overlapped genes between 2 datasets were selected, gene ontology and Kyoto Encyclopedia of Genes and Genomes analyses were performed. The overlapped genes were integrated to construct a protein-protein interaction network and hub genes selection.
Results: We observed 41 overlapped genes between endometrial and trophoblast cells, and future analysis was accomplished in overlapped and nonoverlapped genes. Kyoto Encyclopedia of Genes and Genomes analysis indicated that overlapped genes were significantly enriched in the complement and coagulation cascades, pluripotency of stem cells, and synthesis and degradation of ketone bodies. Gene ontology analysis suggested that the genes were enriched in the cell cycle, apoptosis, and cell division. The top 10 genes included: IRS1, FGF2, MAPK6, MAPK1, MAPK3, MAPK8, MAPK9, PLK1, PRKACA, and PRKCA were identified from the PPI network.
Conclusion: This study identified the key genes and potential molecular pathways underlying the development of RM. This could provide novel insights to determine the possible mechanisms and interventional strategies associated with miscarriage.
Full-Text [PDF 1452 kb]   (315 Downloads) |   |   Full-Text (HTML)  (39 Views)  
Type of Study: Original Article | Subject: Reproductive Genetics

References
1. Practice Committee of the American Society for Reproductive Medicine. Definitions of infertility and recurrent pregnancy loss: A committee opinion. Fertil Steril 2020; 113: 533-535. [DOI:10.1016/j.fertnstert.2019.11.025]
2. Garrido-Gimenez C, Alijotas-Reig J. Recurrent miscarriage: Causes, evaluation and management. Postgrad Med J 2015; 91: 151-162. [DOI:10.1136/postgradmedj-2014-132672]
3. Chen X, Guo D-Y, Yin T-L, Yang J. Non-coding RNAs regulate placental trophoblast function and participate in recurrent abortion. Front Pharmacol 2021; 12: 646521. [DOI:10.3389/fphar.2021.646521]
4. Pollheimer J, Vondra S, Baltayeva J, Beristain AG, Knöfler M. Regulation of placental extravillous trophoblasts by the maternal uterine environment. Front Immunol 2018; 9: 2597. [DOI:10.3389/fimmu.2018.02597]
5. Wu L, Cheng B, Liu Q, Jiang P, Yang J. CRY2 suppresses trophoblast migration and invasion in recurrent spontaneous abortion. J Biochem 2020; 167: 79-87. [DOI:10.1093/jb/mvz076]
6. Mayhew TM. A stereological perspective on placental morphology in normal and complicated pregnancies. J Anat 2009; 215: 77-90. [DOI:10.1111/j.1469-7580.2008.00994.x]
7. Renjith K, Roy DRD, Anthony DJA, Varghese ACV, Sreekutty M, Varma PRVR, et al. Genetic aspects of implantation failure. J Adv Zoology 2023; 44: 498-512.
8. Neykova K, Tosto V, Giardina I, Tsibizova V, Vakrilov G. Endometrial receptivity and pregnancy outcome. J Matern-Fetal Neonatal Med 2022; 35: 2591-2605. [DOI:10.1080/14767058.2020.1787977]
9. Walker ER, McGrane M, Aplin JD, Brison DR, Ruane PT. A systematic review of transcriptomic studies of the human endometrium reveals inconsistently reported differentially expressed genes. Reprod Fertil 2023; 4: e220115. [DOI:10.1530/RAF-22-0115]
10. Bastu E, Demiral I, Gunel T, Ulgen E, Gumusoglu E, Hosseini MK, et al. Potential marker pathways in the endometrium that may cause recurrent implantation failure. Reprod Sci 2019; 26: 879-890. [DOI:10.1177/1933719118792104]
11. Deryabin P, Borodkina A. Stromal cell senescence contributes to impaired endometrial decidualization and defective interaction with trophoblast cells. Hum Reprod 2022; 37: 1505-1524. [DOI:10.1093/humrep/deac112]
12. Pathare ADS, Hinduja I. Endometrial expression of cell adhesion genes in recurrent implantation failure patients in ongoing IVF cycle. Reprod Sci 2022; 29: 513-523. [DOI:10.1007/s43032-021-00708-x]
13. Erboga M, Kanter M. Trophoblast cell proliferation and apoptosis in placental development during early gestation period in rats. Anal Quant Cytopathol Histopathol 2015; 37: 286-294.
14. Zhang X, Wei H. Role of decidual natural killer cells in human pregnancy and related pregnancy complications. Front Immunol 2021; 12: 728291. [DOI:10.3389/fimmu.2021.728291]
15. Crosby D, Glover L, Brennan E, Kelly P, Cormican P, Moran B, et al. Dysregulation of the interleukin-17A pathway in endometrial tissue from women with unexplained infertility affects pregnancy outcome following assisted reproductive treatment. Hum Reprod 2020; 35: 1875-1888. [DOI:10.1093/humrep/deaa111]
16. Makker A, Goel MM, Nigam D, Mahdi AA, Das V, Agarwal A, et al. Aberrant Akt activation during implantation window in infertile women with intramural uterine fibroids. Reprod Sci 2018; 25: 1243-1253. [DOI:10.1177/1933719117737844]
17. Bendridi N, Selmi A, Balcerczyk A, Pirola L. Ketone bodies as metabolites and signalling molecules at the crossroad between inflammation and epigenetic control of cardiometabolic disorders. Int J Mol Sci 2022; 23: 14564. [DOI:10.3390/ijms232314564]
18. Huang J, Yeung AM, Bergenstal RM, Castorino K, Cengiz E, Dhatariya K, et al. Update on measuring ketones. J Diabetes Sci Technol 2024; 18: 714-726. [DOI:10.1177/19322968231152236]
19. Qian M, Wu N, Li L, Yu W, Ouyang H, Liu X, et al. Effect of elevated ketone body on maternal and infant outcome of pregnant women with abnormal glucose metabolism during pregnancy. Diabetes Metab Syndr Obes 2020; 13: 4581-4588. [DOI:10.2147/DMSO.S280851]
20. Whatley EG, Truong TT, Harvey AJ, Gardner DK. Acetoacetate and β-hydroxybutyrate reduce mouse embryo viability via differential metabolic and epigenetic mechanisms. Reprod Biomed Online 2023; 46: 20-33. [DOI:10.1016/j.rbmo.2022.09.018]
21. Agostinis Ch, Mangogna A, Balduit A, Kishore U, Bulla R. A non-redundant role of complement protein C1q in normal and adverse pregnancy. Explor Immunol 2022; 2: 622-636. [DOI:10.37349/ei.2022.00072]
22. Girardi G, Lingo JJ, Fleming SD, Regal JF. Essential role of complement in pregnancy: From implantation to parturition and beyond. Front Immunol 2020; 11: 1681. [DOI:10.3389/fimmu.2020.01681]
23. Spazzapan M, Pegoraro S, Agostinis C, Bulla R. The role of complement component C1q in angiogenesis. Explor Immunol 2023; 3: 574-589. [DOI:10.37349/ei.2023.00122]
24. Laskowski D, Sjunnesson Y, Humblot P, Andersson G, Gustafsson H, Båge R. The functional role of insulin in fertility and embryonic development: What can we learn from the bovine model? Theriogenology 2016; 86: 457-464. [DOI:10.1016/j.theriogenology.2016.04.062]
25. Assaf L, Eid AA, Nassif J. Role of AMPK/mTOR, mitochondria, and ROS in the pathogenesis of endometriosis. Life Sci 2022; 306: 120805. [DOI:10.1016/j.lfs.2022.120805]
26. Tian W, Teng F, Gao J, Gao C, Liu G, Zhang Y, et al. Estrogen and insulin synergistically promote endometrial cancer progression via crosstalk between their receptor signaling pathways. Cancer Biol Med 2019; 16: 55-70. [DOI:10.20892/j.issn.2095-3941.2018.0157]
27. Dejani NN, Nicoletti CF, Argentato PP, Pereira LdS, Saraiva AC, deAssis LM, et al. Maternal plasma transforming growth factor-β1 (TGF-β1) and newborn size: The Araraquara cohort study. J Pediatr 2023; 99: 284-288. [DOI:10.1016/j.jped.2022.11.009]
28. de Ruijter-Villani M, van Boxtel PR, Stout TA. Fibroblast growth factor-2 expression in the preimplantation equine conceptus and endometrium of pregnant and cyclic mares. Theriogenology 2013; 80: 979-989. [DOI:10.1016/j.theriogenology.2013.07.024]
29. Pinto-Bravo P, Rebordão MR, Amaral A, Fernandes C, Galvão A, Silva E, et al. Microvascularization and expression of fibroblast growth factor and vascular endothelial growth factor and their receptors in the mare oviduct. Animals 2021; 11: 1099. [DOI:10.3390/ani11041099]

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb