ANO9 Regulated Cell Cycle in Human Esophageal Squamous Cell Carcinoma

• Published in: Annals of surgical oncology 2020-09, Vol.27 (9), p.3218-3230
• Main Authors: Katsurahara, Keita, Shiozaki, Atsushi, Kosuga, Toshiyuki, Kudou, Michihiro, Shoda, Katsutoshi, Arita, Tomohiro, Konishi, Hirotaka, Komatsu, Shuhei, Kubota, Takeshi, Fujiwara, Hitoshi, Okamoto, Kazuma, Kishimoto, Mitsuo, Konishi, Eiichi, Marunaka, Yoshinori, Otsuji, Eigo
• Format: Article
• Language: English
• Subjects: Anoctamins - genetics; Anoctamins - metabolism; Apoptosis - physiology; Cell Cycle - physiology; Cell Line, Tumor; Cell Movement - physiology; Cell Proliferation - physiology; Esophageal Neoplasms - genetics; Esophageal Neoplasms - metabolism; Esophageal Neoplasms - pathology; Esophageal Squamous Cell Carcinoma - genetics; Esophageal Squamous Cell Carcinoma - metabolism; Esophageal Squamous Cell Carcinoma - pathology; Gene Knockdown Techniques; Humans; Medicine; Medicine & Public Health; Neoplasm Invasiveness; Oncology; Phospholipid Transfer Proteins - genetics; Phospholipid Transfer Proteins - metabolism; Spastin - genetics; Spastin - metabolism; Surgery; Surgical Oncology; Translational Research and Biomarkers
• ISSN: 1068-9265; 1534-4681
• DOI: 10.1245/s10434-020-08368-y

Background Few studies have reported the function and activation mechanism of ANO9 in esophageal squamous cell carcinoma (ESCC). The current study aimed to investigate the role of ANO9 in the regulation of tumor progression. Methods Knockdown experiments with human ESCC cell lines were performed using ANO9 siRNA, and the effects on cell proliferation, the cell cycle, apoptosis, and cellular movement were analyzed. Immunohistochemistry (IHC) analysis was performed on 57 primary tumor samples obtained from ESCC patients. Results In an in vitro study, depletion of ANO9 reduced cell proliferation, invasion, and migration in KYSE150 and KYSE 790 cells. In the cell cycle analysis, depletion of ANO9 increased the number of cells in G 0 /G 1 arrest. In addition, the knockdown of ANO9 increased apoptosis. The results of the microarray analysis indicated that various centrosome-related genes such as CEP120, CNTRL, and SPAST were up- or downregulated in ANO9-depleted KYSE150 cells. The IHC results showed that high expression of ANO9 was associated with poor prognosis. Conclusions The results of the current study suggest that ANO9 regulates the cell cycle via centrosome-related genes in ESCC.