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EM2D9, A monoclonal antibody against integrin α5β1, has potent antitumor activity on endometrial cancer in vitro and in vivo
- Source :
- Cancer Letters. 483:66-74
- Publication Year :
- 2020
- Publisher :
- Elsevier BV, 2020.
-
Abstract
- Endometrial cancer, a type of primary epithelial malignant tumor in the endometrium, is one of the three most common malignant tumors of the female reproductive system. While the incidence of endometrial cancer has been recently rising, its etiology remains unclear. In this study we found that EM2D9, an independently developed monoclonal antibody, specifically recognized endometrial cancer cells; we further determined that EM2D9 target protein was α5β1. In vitro and in vivo experiments showed that EM2D9 inhibited the migration of endometrial cancer cells. Real-time quantitative PCR results showed that the expression of CD151 mRNA in endometrial carcinoma cells significantly decreased after EM2D9 treatment. We also found that EM2D9 affected the FAK signaling pathway. Collectively, these results shed light on a new mechanism for the development of endometrial carcinoma.
- Subjects :
- 0301 basic medicine
Integrins
Cancer Research
medicine.drug_class
Mice, SCID
Tetraspanin 24
Endometrium
Monoclonal antibody
03 medical and health sciences
Antineoplastic Agents, Immunological
0302 clinical medicine
Cell Movement
Mice, Inbred NOD
In vivo
Cell Line, Tumor
medicine
Carcinoma
Animals
Humans
business.industry
Integrin beta1
Endometrial cancer
Antibodies, Monoclonal
Cell migration
medicine.disease
Xenograft Model Antitumor Assays
In vitro
Endometrial Neoplasms
030104 developmental biology
Real-time polymerase chain reaction
medicine.anatomical_structure
Oncology
Focal Adhesion Kinase 1
030220 oncology & carcinogenesis
Cancer research
Female
business
Integrin alpha5beta1
Signal Transduction
Subjects
Details
- ISSN :
- 03043835
- Volume :
- 483
- Database :
- OpenAIRE
- Journal :
- Cancer Letters
- Accession number :
- edsair.doi.dedup.....b5d5979cb4cc7f67c8dfb3b81588a8ae
- Full Text :
- https://doi.org/10.1016/j.canlet.2020.02.019