Article Text

Download PDFPDF
Altered Claudin-4 Expression in Progesterone-Treated Endometrial Adenocarcinoma Cell Line Ishikawa
  1. Pan Xiao-Yu, PhD,
  2. Jin Yan, PhD,
  3. Feng Cui-Ping, MA,
  4. Wang Ya-Nan, PhD,
  5. Lin Hua, BA and
  6. L Hua-Jun, BAi
  1. Department of Obstetrics and Gynecology, China-Japan Friendship Hospital, Beijing, People’s Republic of China.
  1. Address correspondence and reprint requests to Xiao-Yu Pan, PhD, Department of Obstetrics and Gynecology, China-Japan Friendship Hospital, Beijing 100029, People’s Republic of China. E-mail:


Objective To detect the expression change of claudin-4 in Ishikawa endometrial adenocarcinoma cell line in response to progesterone. To determine whether claudin-4 is involved in the anticancer effect of progesterone.

Methods 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was used to determine the 50% inhibitory concentration (IC50) of megestrol acetate (MA) in treating Ishikawa cells. After the Ishikawa cells were treated with MA at IC50, cell apoptosis was examined by flow cytometry and transmission electron microscopy. The messenger RNA and protein expression levels of claudin-4 were further quantified by real-time polymerase chain reaction and Western blot. The localization of claudin-4 was examined by immunofluorescent staining.

Results The IC50 of MA on Ishikawa cells was 15 mg/L incubated for 72 hours. Apoptosis percentage was elevated from 0.07% ± 0.02% to 3.93% ± 0.81% after MA treatment. The expression of claudin-4 at both protein and messenger RNA levels was significantly decreased after the treatment of MA (P < 0.05). The localization of claudin-4 transferred from cytomembrane to cytoplasm and nucleus.

Conclusion Megestrol acetate can inhibit the growth of Ishikawa cells. It may work through decreasing claudin-4 expression and cell apoptosis. The localization change of claudin-4 may also be involved in the anticancer effect of progesterone.

  • Endometrial carcinoma
  • Progesterone
  • Claudin-4
  • Apoptosis

Statistics from

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.


  • This work was supported by the National Natural Science Foundation of China (No. 30901599) and a project grant from China-Japan Friendship Hospital.

  • The authors declare no conflicts of interest.