Aldolase A promotes epithelial‐mesenchymal transition to increase malignant potentials of cervical adenocarcinoma. Issue 8 (30th June 2020)

• Record Type: Journal Article
• Authors: Saito, Yuki; Takasawa, Akira; Takasawa, Kumi; Aoyama, Tomoyuki; Akimoto, Taishi; Ota, Misaki; Magara, Kazufumi; Murata, Masaki; Hirohashi, Yoshihiko; Hasegawa, Tadashi; Sawada, Norimasa; Saito, Tsuyoshi; Osanai, Makoto
• Is Part Of: Cancer science. Volume 111:Issue 8(2020)
• Page Start: 3071
• Page End: 3081
• Publication Date: 2020-06-30
• Subjects: aldolase A -- cervical adenocarcinoma -- epithelial‐mesenchymal transition -- hypoxia‐inducible factor‐1α -- metabolic reprogramming; Cancer -- Periodicals; Neoplasms -- Periodicals; Research -- Periodicals; Electronic journals; 616.994005
• DOI: 10.1111/cas.14524
• Languages: English
• ISSNs: 1347-9032

Abstract

Abstract: Recent studies have revealed that metabolic reprogramming is closely associated with epithelial‐mesenchymal transition (EMT) during cancer progression. Aldolase A (ALDOA) is a key glycolytic enzyme that is highly expressed in several types of cancer. In this study, we found that ALDOA is highly expressed in uterine cervical adenocarcinoma and that high ALDOA expression promotes EMT to increase malignant potentials, such as metastasis and invasiveness, in cervical adenocarcinoma cells. In human surgical specimens, ALDOA was highly expressed in cervical adenocarcinoma and high ALDOA expression was correlated with lymph node metastasis, lymphovascular infiltration, and short overall survival. Suppression of ALDOA expression significantly reduced cell growth, migration, and invasiveness of cervical cancer cells. Aldolase A expression was partially regulated by hypoxia‐inducible factor‐1α (HIF‐1α). Shotgun proteome analysis revealed that cell‐cell adhesion‐related proteins were significantly increased in ALDOA‐overexpressing cells. Interestingly, overexpression of ALDOA caused severe morphological changes, including a cuboidal‐to‐spindle shape shift and reduced microvilli formation, coincident with modulation of the expression of typical EMT‐related proteins. Overexpression of ALDOA increased migration and invasion in vitro. Furthermore, overexpression of ALDOA induced HIF‐1α, suggesting a positive feedback loop between ALDOA and HIF‐1α. In conclusion, ALDOA is overexpressed in cervical adenocarcinoma and contributes to malignant potentials of tumor cells through modulation of HIF‐1α signaling. The feedback loop between ALDOA and HIF‐1α could become a therapeutic target to improve the prognosis of this malignancy. Abstract : Aldolase A (ALDOA) overexpression caused epithelial‐mesenchymal transition‐like morphological alterations in cervical adenocarcinoma cells (A‐C). ALDOA‐overexpressing cells showed increased stress fiber formation (D‐F, red) and reduced E‐cadherin expression (D‐F, green) and microvilli formation (G).