THE ROLE OF GROWTH FACTORS IN TROPHOBLAST INVASION AND THEIR ASSOCIATION WITH THE PATHOLOGICAL COURSE OF PREGNANCY
https://doi.org/10.36604/1998-5029-2019-74-111-118
Abstract
About the Author
N. G. PrikhodkoRussian Federation
MD, Postgraduate Student, Laboratory of Mechanisms of Etiopathogenesis and Recovery Processes of the Respiratory System at Non-Specific Lung Diseases
22 Kalinina Str., Blagoveshchensk, 675000, Russian Federation
References
1. Keshavarzi F., Shahrakipoor M., Teimoori B., Yaghmaei M., Narooei-Nejad M., Rasooli A., Salimi S. Association of the placental VEGF promoter polymorphisms and VEGF mRNA expression with preeclampsia. Clin. Exp. Hypertens. 2019; 41(3):274–279. doi: 10.1080/10641963.2018.1469644
2. Bоtasheva T.L., Linde V.A., Sargsyan O.D., Ermolova N.V., Gimbut V.S., Zheleznyakova E.V., Mikhelson A.A. Angiogenic factors and cytokines levels in maternal blood may predict birth outcomes and its connection to the fetal gender. Sovremennye problemy nauki i obrasovaniya 2014; 6:1057 (in Russian).
3. Kopp H.G., Placke T., Salih Y.R. Platelet-derived transforming growth factor-beta down-regulates NKG2D thereby inhibiting natural killer cell antitumor reactivity. Cancer Res. 2009; 69(19):7775–7783. doi: 10.1158/0008-5472.CAN-09-2123
4. Burlev V.A. The role of endometrial blood vessels in the formation of the trophoblast and placenta. Problemy reproduktsii 2016; 22(6):8–17 (in Russian). doi:10.17116/repro20162268-17
5. Liu T., Zheng X., Li Q., Chen J., Yin Z., Xiao J., Zhang D., Li W., Qiao Y., Chen S. Role of human cytomegalovirus in the proliferation and invasion of extravillous cytotrophoblast isolated from early placentae. Int. J. Clin .Exp. Med. 2015; 8(10):17248–17260.
6. Veropotvelyan P.N., Veropotvelyan N.P., Guzhevskaya I.V. Cytokines in the mother-placenta-fetus system in physiological and pathological advancement of pregnancy. Zdorov'e zhenshchiny 2013; 1 (77):126–129 (in Russian).
7. Magdoud K., Granados Herbepin V., Messaoudi S., Hizem S., Bouafia N., Almawi W.Y., Mahjoub T., Touraine R. Genetic variation in TGFB1 gene and risk of idiopathic recurrent pregnancy loss. Mol. Hum. Reprod. 2013; 19(7):438–443. doi: 10.1093/molehr/gat012
8. Vorontsova Z.A., Zhilyaeva O.D., Gureev A.S. Morphofunctional peculiarities of placentes in accuracy and somatic pathology (literature review). Vestnik novykh meditsinskikh tekhnologiy 2018; 25(3):34–43 (in Russian). doi: 10.24411/1609-2163-2018-16147
9. Makris A., Thornton C., Thompson J., Thomson S., Martin R., Ogle R., Waugh R., McKenzie P., Kirwan P., Hennessy A. Uteroplacental ischemia results in proteinuric hypertension and elevated sFLT-1. Kidney Int. 2007; 71(10):977–984. doi:10.1038/sj.ki.5002175
10. Gazieva I.A, Chistyakova G.N., Dankova I.V., Selivanov O.L. Immune mechanisms of the regulation of fetoplacental complex development. Ural'skiy meditsinskiy zhurnal 2008; 12(52):80–85 (in Russian).
11. Meoli E.M., Oh U., Grant C.W., Jacobson S. TGF-beta signaling is altered in the peripheral blood of subjects with multiple sclerosis. J. Neuroimmunol. 2011; 230(1-2):164–168. doi:10.1016/j.jneuroim.2010.10.028
12. Davydov A.I., Agrba I.B., Voloschuk I.N. The pathogenesis of placenta attachment pathology: the role of growth factors and other immunohistochemical markers. Voprosy ginekologii, akusherstva i perinatologii 2012; 11(1):48–54 (in Russian).
13. Nadeem L., Munir S., Fu G., Baczyk D., Caniggia I., Lye S., Peng C. Nodal signals through activin receptor-like kinase 7 to inhibit trophoblast migration and invasion: implication in the pathogenesis of preeclampsia. Am. J. Pathol. 2011; 178(3):1177–1189. doi:10.1016/j.ajpath.2010.11.066
14. Demchenko N.S., Bashmakova N.V., Tretyakova T.B. Pathogenesis of the pregnancy loss: role of the vascular endothelial growth factor (VEGF-A). Ural’skiy meditsinskiy zhurnal 2012; 11(103):6 (in Russian).
15. Nejabati H.R., Latifi Z., Ghasemnejad T., Fattahi A., Nouri M. Placental growth factor (PIGF) as an angiogenic/inflammatory switcher: lesson from early pregnancy losses. Gynecol. Endocrinol. 2017; 33(9):668–674. doi:10.1080/09513590.2017.1318375
16. Ivanets T.Yu., Kan N.E., Tyutyunyuk V.G., Bezzubenko Yu.V., Ibragimov R.R. The role of the soluble fms-like tyrosin kinase-1/the placental growth factor ratio in the diagnostics of preeclampsia in physiological pregnancy and pregnancy after IVF. Akusherstvo i ginikologiya 2018; 3:37–42 (in Russian). doi:10.18565/aig.2018.3.37-42
17. Plaisier M., Dennert I., Rost E., Koolwijk P., van Hinsbergh V.W., Helmerhorst F.M. Decidual vascularization and the expression of angiogenic growth factors and proteases in first trimester spontaneous abortions. Hum. Reprod. 2009; 24(1):185–197. doi:10.1093/humrep/den296
18. Igitova M.B., Dmitrienko K.V. Prediction unfavorable perinatal outcomes with the help of maternal serum placental growth factor concentration. Mat' i ditya v Kuzbasse 2014; (59):38–41 (in Russian).
19. Prosler J., Chen Q., Chamley L., James J.L. The relationship between TGFbeta, low oxygen and the outgrowth of extravillous trophoblasts from anchoring villi during the first trimestr of pregnancy. Cytokine 2014; 68(1):9–15. doi:10.1016/j.cyto.2014.03.001
20. Kazachkov E.L., Kazachkova E.A., Vorobyov I.V., Pashirova N.V. Structural features angiogenesis of placenta in women with cardiovascular disease: histological and immunohistochemical characteristics of placenta. Ural'skiy meditsinskiy zhurnal 2016; 3(136)101–106 (in Russia).
21. Sahu M.B., Deepak V., Gonzales S.K., Rimawi B., Watkins K.K., Smith A.K., Badell M.L., Sidell N., Rajakumar A. Decidual cells from women with preeclampsia exhibit inadequate decidualization and reduced sFlt1 suppression. Pregnancy Hypertens. 2019; 15:64–71. doi:10.1016/j.preghy.2018.11.003
22. Magomedova Sh. M. Modern aspects of etiology and pathogenesis of placental insufficiency and preeclampsia (review). Vestnik Dagestanskoy gosudarstvennoy meditsinskoy akademii 2013; 4(9):60–64 (in Russian).
23. Shchyogolev A.L., Dubova E.A., Pavlova K.A., Lyapin V.M., Sukhikh G.T. Expression of antiangiogenic factors in the placental structures in pre-eclampsia. Bull. Exp. Biol. Med. 2012; 154(2):287–291. doi:10.1007/s10517-012-1932-0
24. Makarov O.V., Volkova E.V., Lysyuk E.Yu., Kopylova Yu.V., Dzhokhadze L.S. Role of angiogenic growth factors in the pathogenesis of preeclampsia and placental insufficiency. Akusherstvo i ginekologiya 2014; 12:64–70 (in Russian).
25. Su M.T., Lin S.H., Chen Y.C. Genetic association studies of angiogenesis and vasoconstriction-related genes in women with recurrent pregnancy loss: a systematic review and meta-analysis. Hum. Reprod. Update 2011; 17(6):803–812. doi:10.1093/humupd/dmr027
26. Marakhovskaya T.A. Role of growth factors in miscarriage. Uchenye sapiski Krymskogo federal'nogo universiteta imeni V.I. Vernadskogo. Biologiya. Khimiya 2018; 4(2):91–111 (in Russian).
27. Venkata Surekha M., Singh S., Sarada K., Sailaja G., Balakrishna N., Srinivas M., Uday Kumar P. Study on the effect of severity of maternal iron deficiency anemia on regulators of angiogenesis in placenta. Fetal Pediatr. Pathol. 2019; 38(5):361–375. doi:10.1080/15513815.2019.1587120
28. Murashko A.V., Magomedova Sh.M. Role of growth factors in the development of placental failure and pre-eclampsia. Arkhiv akusherstva i ginikologii im. V.F. Snegireva 2015; 2(3):25–28 (in Russian).
29. Visan V., Scripcariu I.S., Socolov D., Costescu A., Rusu D., Socolov R., Avasiloaiei A., Boiculese L., Dimitriu C. Better prediction for FGR (fetal growth restriction) with the sFlt-1/PIGF ratio: A case-control study. Medicine (Baltimore) 2019; 98(26):e16069. doi:10.1097/MD.0000000000016069
30. Orlov A.V., Kudinova E.I. Aspects etiopatogenesis of the development to insufficiency of placenta and fetal growth retardation. Zhurnal fundamental'noy meditsiny i biologii 2016; 4:4–10 (in Russian).
31. Wang P., Fan J., Chen Z., Meng Z.Q., Meng Z.Q., Luo J.M., Lin J.H., Zhou Z.H., Chen H., Wang K., Xu Z.D., Liu L.M. Low-level expression of Smad7 correlates with lymph node metastasis and poor prognosis in patients with pancreatic cancer. Ann. Surg. Oncol. 2009; 16(4):826–835. doi:10.1245/s10434-008-0284-5
32. Pitskhelauri E.G., Strizhakov A.N., Timokhina E.V., Ignatko E.V., Belousova B.S. Implantation problems and risks of pregnancy complications after assisted reproductive technologies. Voprosy ginekologii, akusherstva i perinatologii 2017; 16(2): 34–39 (in Russian). doi: 10.20953/1726-1678-2017-2-34-39
33. Rudyuk L.A., Reshetnikova O.S. Angiogenesis-related factors in the placenta of pregnant women with congenital heart diseases. Arkhiv patologii 2019; 81(4):33–38 (in Russian). doi: 10.17116/patol20198104133
34. Rud'ko A.S., Efendieva M.Kh., Budzinskya M.V., Karpilova M.A. Influence of vascular endothelial growth factor on angiogenesis and neurogenesis. Vestnik oftal'mologii 2017; 133(3):75–81 (in Russian). doi: 10.17116/oftalma2017133375-80
35. Ryabova S.A., Tezikov Yu.V., Lipatov I.S., Zhernakova E.V., Tabelskaya T.V. Opportunities of forecasing fetal pathology at placental insufficiency since the first trimester of pregnancy. Sovremennye problem nauki i obrazovaniya 2016; 5:44 (in Russian).
36. Sidelnikova V.M., Sukhih G.T. Miscarriage: A Guide for Practitioners. Moscow: Meditsinskoe informatsionnoe agentstvo; 2010 (in Russian).
37. Sofwat Kh., Beketova G.B. The physiology and regulation of human fetal growth (part I). Pediatriya. Vostochnaya Evropa. 2016; 4(3):504–521 (in Russian).
38. Strizhakov A.N., Timokhina E.V., Tarabrina T.V. Clinical significance of insulin-like growth factor in the development of fetal growth retardation syndrome. Voprosy ginikologii, akusherstva i perinatologii 2009; 8(5): 5–9 (in Russian).
39. Fаmina M.P., Divakova T.S., Rzheusskaya L.D. Effect of otilonium bromide on intensity of chronic abdominal pain. Meditsinskiye novosti 2014; 3:63–67. (in Russian)
40. El'zhorukaeva Zh.A., Mikhel'son A.A., Sargsyan O.D., Grigoryants A.A., Arutyunyan T.G., Kogan O.M. The role of growth factors in miscarriage. Tavricheskiy mediko-biologicheskiy vestnik 2016; 19(2):158–161 (in Russian).
41. Yakovleva N.Yu., Khazova E.L., Vasil'eva E.Yu., Zazerskaya E.I. Ratio of angiogenicand anti-angiogenic factors in preeclampsia. Arterial'naya gipertenzhiya 2016; 22(5):488–494 (in Russian). doi:10.18705/1607-419X-2016-22-5-488-494
42. Yakovleva N.Yu., Vasilyeva E.Yu., Shelepova E.S., Ryabokon' N.R., Khazova E.L., Buravleva K., Kuznetsova L.V., Zazerskaya E.I. Investigation of time course of changes in the concentrations of angiogenic factors on the length of physiological pregnancy. Akusherstvo i ginikologiya 2016; 8:49–53 (in Russian). doi: 10.18565/aig.2016.8.49-53
43. Ali L.E., Salih M.M., Elhassan E.M., Mohmmed A.A., Adam I. Placental growth factor, vascular endothelial growth factor, and hypoxia-inducible factor-1α in the placentas of women with pre-eclampsia. J. Matern. Fetal Neonatal Med. 2019; 32(16):2628-2632. doi: 10.1080/14767058.2018.1443066
44. Amirchaghmaghi E, Rezaei A, Moini A, Roghaei MA, Hafezi M, Aflatoonian R. Gene expression analysis of VEGF and its receptors and assessment of its serum level in unexplained recurrent spontaneous abortion. Cell J. 2015; 16(4):538–545. doi: 10.22074/cellj.2015.498
45. Andrievskaya I.A., Lutcenko M.T., Babenko O.P. Specific and non-specific factors of humoral immunity as markers for pregnancy loss in women with cytomegalovirus infection. International Journal of Biomedicine. 2015; 5(4):184–187. doi: 10.21103/Article5(4)_OA2
46. Arroyo J., Price M., Straszewski-Chaves S., Torry R.J., Mor G., Torry D.S. XIAP protein is induced by placenta growth factor (PIGF) and decreased during preeclampsia in trophoblast cell. Syst. Biol. Reprod. Med. 2014; 60(5):263–273. doi: 10.3109/19396368.2014.927540.
47. Chau K., Hennessy A., Makris A. Placental growth factor and pceeclampsia. J. Hum. Hypertens. 2017; 31(12):782–786. doi: 10.1038/jhh.2017.61.
48. Chang Y.S., Chen C.N., Jeng S.F., Su Y.N., Chen C.Y., Chju H.C., Tsao P.N., Hsieh W.S. The sFlt-1/PlGF ratio as a predictor for poor pregnancy and neonatal outcomes. Pediatr. Neonatal. 2017; 58(6):529–533. doi: 10.1016/j.pedneo.2016.10.005
49. Guimaraes G.C., Alves L.A., Betarelli R.P., Guimarães C.S.-O.,Helmo F.R., Pereira Júnior C.D., Corrêa R.R.-M., Zangeronimo M.G. Expression of vascular endothelial growth factor (VEGF) and factor VIII in the gilt placenta and its relation to fetal development. Theriogenology 2017; 92:63–68. doi: 10.1016/j.theriogenology.2017.01.002
50. Hastie R., Brownfoot F.C., Pritchard N., Hannan N.J., Cannon P., Nguyen V., Palmer K., Beard S., Tong S., Kaitu'u-Lino T.J. EGFR (epidermal growth factor receptor) signaling and the mitochondria regulate sFlt-1 (soluble FMS-like tyrosine kinase-1) secretion. Hypertension. 2019; 73(3):659-670. doi: 10.1161/HYPERTENSIONAHA.118.12300
51. Hoeller A., Ehrlich L., Golic M., Herse F., Perschel F.H., Siwetz M., Henrich W., Dechend R., Huppertz B., Verlohren S. Placental expression of sFlt-1 and PIGF in early preeclampsia vs. early IUGR vs. age-matched healthy pregnancies. Hyprtens. Pregnancy 2017; 36(2):151–160. doi: 10.1080/10641955.2016.1273363
52. Hoffman J., Ossada V., Weber M., Stepan H. An intermediate sFlt-1/PIGF ratio indicates an increased risk for adverse pregnancy outcome. Pregnancy Hypertens. 2017; 10:165–170. doi: 10.1016/j.preghy.2017.08.003
53. Keskin U., Ulubay M., Dede M., Ozgurtas T., Koçyiğit Y.K., Aydin F.N., Ergün A. The relationship between the VEGF/sVEGFR-1 ratio and threatened abortion. Arch. Gynekol. Obstet. 2015; 291(3):557–561. doi: 10.1007/s00404-014-3452-9
54. Keshavarzi F., Shahrakipoor M., Teimoori B., Yaghmaei M., Narooei-Nejad M., Rasooli A., Salimi S. Association of the placental VEGF promoter polymorphisms and VEGF mRNA expression with preeclampsia. Clin. Exp. Hypertens. 2019; 41(3):274–279. doi: 10.1080/10641963.2018.1469644
55. Kopp H.G., Placke T., Salih Y.R. Platelet-derived transforming growth factor-beta down-regulates NKG2D thereby inhibiting natural killer cell antitumor reactivity. Cancer Res. 2009; 69(19):7775–7783. doi: 10.1158/0008-5472.CAN-09-2123
56. Liu T., Zheng X., Li Q., Chen J., Yin Z., Xiao J., Zhang D., Li W., Qiao Y., Chen S. Role of human cytomegalovirus in the proliferation and invasion of extravillous cytotrophoblast isolated from early placentae. Int. J. Clin .Exp. Med. 2015; 8(10):17248–17260.
57. Magdoud K., Granados Herbepin V., Messaoudi S., Hizem S., Bouafia N., Almawi W.Y., Mahjoub T., Touraine R. Genetic variation in TGFB1 gene and risk of idiopathic recurrent pregnancy loss. Mol. Hum. Reprod. 2013; 19(7):438–443. doi: 10.1093/molehr/gat012
58. Makris A., Thornton C., Thompson J., Thomson S., Martin R., Ogle R., Waugh R., McKenzie P., Kirwan P., Hennessy A. Uteroplacental ischemia results in proteinuric hypertension and elevated sFLT-1. Kidney Int. 2007; 71(10):977–984. doi:10.1038/sj.ki.5002175
59. Meoli E.M., Oh U., Grant C.W., Jacobson S. TGF-beta signaling is altered in the peripheral blood of subjects with multiple sclerosis. J. Neuroimmunol. 2011; 230(1-2):164–168. doi:10.1016/j.jneuroim.2010.10.028
60. Nadeem L., Munir S., Fu G., Baczyk D., Caniggia I., Lye S., Peng C. Nodal signals through activin receptor-like kinase 7 to inhibit trophoblast migration and invasion: implication in the pathogenesis of preeclampsia. Am. J. Pathol. 2011; 178(3):1177–1189. doi:10.1016/j.ajpath.2010.11.066
61. Nejabati H.R., Latifi Z., Ghasemnejad T., Fattahi A., Nouri M. Placental growth factor (PIGF) as an angiogenic/inflammatory switcher: lesson from early pregnancy losses. Gynecol. Endocrinol. 2017; 33(9):668–674. doi:10.1080/09513590.2017.1318375
62. Plaisier M., Dennert I., Rost E., Koolwijk P., van Hinsbergh V.W., Helmerhorst F.M. Decidual vascularization and the expression of angiogenic growth factors and proteases in first trimester spontaneous abortions. Hum. Reprod. 2009; 24(1):185–197. doi:10.1093/humrep/den296
63. Prosler J., Chen Q., Chamley L., James J.L. The relationship between TGFbeta, low oxygen and the outgrowth of extravillous trophoblasts from anchoring villi during the first trimestr of pregnancy. Cytokine 2014; 68(1):9–15. doi:10.1016/j.cyto.2014.03.001
64. Sahu M.B., Deepak V., Gonzales S.K., Rimawi B., Watkins K.K., Smith A.K., Badell M.L., Sidell N., Rajakumar A. Decidual cells from women with preeclampsia exhibit inadequate decidualization and reduced sFlt1 suppression. Pregnancy Hypertens. 2019; 15:64–71. doi:10.1016/j.preghy.2018.11.003
65. Shchyogolev A.L., Dubova E.A., Pavlova K.A., Lyapin V.M., Sukhikh G.T. Expression of antiangiogenic factors in the placental structures in pre-eclampsia. Bull. Exp. Biol. Med. 2012; 154(2):287–291. doi:10.1007/s10517-012-1932-0
66. Su M.T., Lin S.H., Chen Y.C. Genetic association studies of angiogenesis and vasoconstriction-related genes in women with recurrent pregnancy loss: a systematic review and meta-analysis. Hum. Reprod. Update 2011; 17(6):803–812. doi:10.1093/humupd/dmr027
67. Venkata Surekha M., Singh S., Sarada K., Sailaja G., Balakrishna N., Srinivas M., Uday Kumar P. Study on the effect of severity of maternal iron deficiency anemia on regulators of angiogenesis in placenta. Fetal Pediatr. Pathol. 2019; 38(5):361–375. doi:10.1080/15513815.2019.1587120
68. Visan V., Scripcariu I.S., Socolov D., Costescu A., Rusu D., Socolov R., Avasiloaiei A., Boiculese L., Dimitriu C. Better prediction for FGR (fetal growth restriction) with the sFlt-1/PIGF ratio: A case-control study. Medicine (Baltimore) 2019; 98(26):e16069. doi:10.1097/MD.0000000000016069
69. Wang P., Fan J., Chen Z., Meng Z.Q., Meng Z.Q., Luo J.M., Lin J.H., Zhou Z.H., Chen H., Wang K., Xu Z.D., Liu L.M. Low-level expression of Smad7 correlates with lymph node metastasis and poor prognosis in patients with pancreatic cancer. Ann. Surg. Oncol. 2009; 16(4):826–835. doi:10.1245/s10434-008-0284-5
Review
For citations:
Prikhodko N.G. THE ROLE OF GROWTH FACTORS IN TROPHOBLAST INVASION AND THEIR ASSOCIATION WITH THE PATHOLOGICAL COURSE OF PREGNANCY. Bulletin Physiology and Pathology of Respiration. 2019;(74):111-118. (In Russ.) https://doi.org/10.36604/1998-5029-2019-74-111-118