Explanation of fetal murine retinae to the chorioallantoic membrane of the chicken embryo

1992 ◽  
Vol 41 (1) ◽  
pp. 53-64 ◽  
Author(s):  
Krystel R. Huxlin ◽  
Ann Jervie Sefton ◽  
Judith Furby
2002 ◽  
Vol 400 (2) ◽  
pp. 188-198 ◽  
Author(s):  
E Giannopoulou ◽  
P Katsoris ◽  
C Polytarchou ◽  
E Papadimitriou

Nanoscale ◽  
2012 ◽  
Vol 4 (8) ◽  
pp. 2720 ◽  
Author(s):  
Xi Liu ◽  
Xiumei Wang ◽  
Akihiro Horii ◽  
Xiujuan Wang ◽  
Lin Qiao ◽  
...  

Dose-Response ◽  
2018 ◽  
Vol 16 (2) ◽  
pp. 155932581877248 ◽  
Author(s):  
Lina Šlekienė ◽  
Donatas Stakišaitis ◽  
Ingrida Balnytė ◽  
Angelija Valančiūtė

The study aims to test the effect of different sodium valproate (NaVP) doses on small cell lung cancer NCI-H146 cells tumor in chicken embryo chorioallantoic membrane (CAM) model. Xenografts were investigated in the following groups: nontreated control and 5 groups treated with different NaVP doses (2, 3, 4, 6, and 8 mmol/L). Invasion of tumors into CAM in the nontreated group reached 76%. Tumors treated with 8 mmol/L NaVP doses significantly differed in tumor invasion frequency from the control and those treated with 2 mmol/L ( P < .01). The calculated probability of 50% tumor noninvasion into CAM was when tumors were treated with 4 mmol/L of NaVP. Number of p53-positive cells in tumors was significantly reduced when treated with NaVP doses from 3 to 8 mmol/L as compared with control; number of EZH2-positive cells in control significantly differed from all NaVP-treated groups. No differences in p53- and EZH2-positive cell numbers were found among 4, 6, and 8 mmol/L NaVP-treated groups. Invaded tumors had an increased N-cadherin and reduced E-cadherin expression. The results indicate the increasing NaVP dose to be able to inhibit tumors progression. Expression of p53 and EZH2 may be promising target markers of therapeutic efficacy evaluation.


Angiogenesis ◽  
2010 ◽  
Vol 13 (4) ◽  
pp. 281-292 ◽  
Author(s):  
Patrycja Nowak-Sliwinska ◽  
Judy R. van Beijnum ◽  
Maaike van Berkel ◽  
Hubert van den Bergh ◽  
Arjan W. Griffioen

2019 ◽  
Vol 19 (1) ◽  
pp. 67-71
Author(s):  
Shaikha S. Al-Qahdi ◽  
Nada Alzohari ◽  
Abrar Y. Alsaid ◽  
Anas A. Ashour ◽  
Tahar Aboulkassim ◽  
...  

The aim of this study is to explore the outcome of Teucrium polium (TP) medicinal plant consumption on the early stage of fetal development. We used the chicken embryo at 3 days of incubation as a model to evaluate the effect of TP plant extract during embryogenesis. In addition, quantitative polymerase chain reaction (qPCR) was applied to explore the expression of six genes related to cell proliferation, apoptosis, sur­vival, angiogenesis, and migration. Our data revealed that TP exposure inhibits angiogenesis of the chicken embryo and its chorioallantoic membrane. In addition, we found that TP extract significantly harms the normal development of the embryos since around 95% of TP-exposed embryos died after 1–3 days of treatment. Macroscopic examination did not show any anomalies in these embryos. However, qPCR analysis of activation transcription factor-3, B-cell lymphoma-2, caspase 8, inhibin subunit beta A, vascular endothelial growth factor-C, and Cadherin-6 type-2 genes revealed that these genes are considerably deregulated in heart and brain tissues from TP-exposed embryos in comparison with their matched tissues from unexposed ones. Our study implies that TP plant can have very toxic effects on the early stage of the embryo. Therefore, it is important to alert expectant women to avoid the use of this medicinal plant during pregnancy.


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