
@Article{096504017X14912172235777,
AUTHOR = {Yinghua Li, Songyi Li, Lili Huang},
TITLE = {Knockdown of Rap2B, a Ras Superfamily Protein, Inhibits Proliferation,  Migration, and Invasion in Cervical Cancer Cells via Regulating  the ERK1/2 Signaling Pathway},
JOURNAL = {Oncology Research},
VOLUME = {26},
YEAR = {2018},
NUMBER = {1},
PAGES = {123--130},
URL = {http://www.techscience.com/or/v26n1/56624},
ISSN = {1555-3906},
ABSTRACT = {Rap2B, belonging to the Ras superfamily, has been implicated in cancer development and functions as a tumor 
promoter. However, the role of Rap2B in cervical cancer is unknown. In this study, we investigated the expression pattern and biological functions of Rap2B in cervical cancer. The results showed that Rap2B was overexpressed in cervical cancer tissues and cell lines. Knockdown of Rap2B inhibited the proliferation, migration, 
and invasion of cervical cancer cells. In addition, our tumorigenesis assay showed that Rap2B knockdown suppressed cervical cancer cell growth and metastasis in vivo. We also found that the ERK1/2 signaling pathway 
is involved in the inhibitory effect of Rap2B knockdown on cervical cancer development. In conclusion, we 
suggest that Rap2B is an oncogene and may be a promising therapeutic target for cervical cancer.},
DOI = {10.3727/096504017X14912172235777}
}



