A cohort of samples from Mexican patients with normal and premalignant lesions of the uterine cervix was tested for RIPOR2 expression, formed by 17 normal HPV-negative cervical samples, 7 normal HPV-positive cervical samples, 20 low-grade, and 15 high-grade cervical premalignant lesions, kindly provided by the Instituto Nacional de Salud Pública (INSP). In addition, 19 cervical cancer samples from the Tumor BioBank from the Instituto Nacional de Cancerología of Mexico City (INCan) were included. The protocol was revised and accepted on February 2017, by the Scientific and Ethical committees of INCan Ref. (017/007/IBI)(CEI/1144/17). All patients whose samples were utilized in this study agreed and signed the informed consent.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.