Channelpedia

PubMed 24062569


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Kv10.1



Title: Ether a-go-go-1 potassium channels are expressed in cervical cytologies from pregnant patients and are regulated by progesterone.

Authors: Ana Ramírez, Luz M Hinojosa, José D J Gonzales, Daniel Montante-Montes, Braulio Martínez-Benítez, Ricardo Aguilar-Guadarrama, Armando Gamboa-Dominguez, Flavia Morales, Adela Carrillo-García, Marcela Lizano, Rocío García-Becerra, Lorenza Díaz, Alma Y Vázquez-Sánchez, Javier Camacho

Journal, date & volume: Reproduction, 2013 Sep 23 , ,

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24062569


Abstract
Potassium voltage-gated channel, subfamily H (eag-related), member 1 (KCNH1) potassium channels are potential tumour markers and cancer therapeutic targets and are up-regulated by oestrogens and human papilloma virus (HPV) oncogenes. However, the role of KCNH1 in normal tissues is poorly understood, and its expression in pregnancy is unknown. We wondered whether KCNH1 channels are expressed in cervical cells from pregnant patients and whether progesterone (P4) regulates KCNH1. The association with HPV was also investigated. KCNH1 protein expression was studied by immunocytochemistry in liquid-based cervical cytologies; 93 samples were obtained from pregnant patients at different trimesters, and 15 samples were obtained from non-pregnant women (controls). The presence of HPV was studied by PCR with direct sequencing and nested multiplex PCR. HeLa cervical cancer cells were transfected with human progesterone receptor-B (PR-B) and treated with P4. KCNH1 mRNA expression in these cultures was studied by real-time PCR. KCNH1 protein was detected in 100% of the pregnancy samples and in 26% of the controls. We found 18 pregnant patients infected with HPV and detected 14 types of HPV. There was no association between the percentage of cells expressing KCNH1 and either the presence or type of HPV. P4 induced KCNH1 mRNA and protein expression in cells transfected with human PR-B. No regulation of KCNH1 by P4 was observed in non-transfected cells. We show for the first time the expression of an ion channel during human pregnancy at different trimesters and KCNH1 regulation by P4 in human cells. These data raise a new research field for KCNH1 channels in human tissues.