cervical adenocarcinoma
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2022 ◽  
Vol 164 (1) ◽  
pp. 19
Author(s):  
Victoria Cerda ◽  
Christopher Mayer ◽  
Marla Scott ◽  
Kenneth Kim ◽  
Andrew Li ◽  
...  

2021 ◽  
Author(s):  
Mengzhu Zhang ◽  
Tohru Kiyono ◽  
Kazunori Aoki ◽  
Naoki Goshima ◽  
Shin Kobayashi ◽  
...  

2021 ◽  
Vol 72 ◽  
pp. 103144
Author(s):  
Abdullah Saleh AlQattan ◽  
Afnan Amro Alqutub ◽  
Jumana Husain Masoudi ◽  
Maha Abdulaziz M. Alassaf ◽  
Nabeel Mansi

2021 ◽  
pp. 27-28
Author(s):  
S. Sharnitha ◽  
R. Niranjana ◽  
P. Dhanasekar ◽  
Sarah Grace Priyadharshini

Minimal deviation adenocarcinoma is a subtype of cervical adenocarcinoma and accounts for 1-3% of cervical adenocarcinoma . It is also known as adenoma malignum. We report a case of 55 year old postmenopausal women with complaints of low back pain, on examination cervix was replaced by indurated growth and was diagnosed as minimal deviation adenocarcinoma of cervix by biopsy


2021 ◽  
Author(s):  
S Álvarez Sánchez ◽  
JM Barreiro García ◽  
M Marti Sopeña ◽  
JJ Delgado Espeja ◽  
JA Solano Calvo ◽  
...  

2021 ◽  
Vol 12 (10) ◽  
Author(s):  
Sijia Liu ◽  
Lina Gu ◽  
Nan Wu ◽  
Jiayu Song ◽  
Jiazhuo Yan ◽  
...  

AbstractCervical adenocarcinoma is an important disease that affects young women and it has a high mortality and poor prognosis. Denticleless E3 ubiquitin protein ligase homolog (DTL) gene with oncogenic function has been evaluated in several cancers. Through this study, we aimed to clarify the clinical and molecular characteristics of cervical adenocarcinoma involving overexpression of DTL and elucidate its molecular mechanism. Bioinformatics analysis was performed through multiple databases. RNA sequencing was used to obtain differentially expressed genes after DTL was overexpressed in cells. The role of DTL in cervical adenocarcinoma was explored through in vitro and in vivo experiments. We found that DTL has an unfavorable prognostic implication for patients with cervical adenocarcinoma. Overexpression of DTL induced the migration and invasion of tumor cells in vitro and promoted intra-pulmonary metastasis in vivo. In addition, DTL activated JNK through RAC1 and upregulated FOXO1 to induce epithelial–mesenchymal transition, and the migration and invasion of tumor cells. Therefore, we conclude that overexpression of DTL enhanced cell motility and promoted tumor metastasis of cervical adenocarcinoma by regulating the RAC1-JNK-FOXO1 axis. These results suggest that DTL may become a potential therapeutic target for antitumor metastasis of cervical adenocarcinoma.


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