Baicalein suppresses HER2‐mediated malignant transformation of HER2‐overexpressing ovarian cancer cells by downregulating HER2 gene expression

Author:

Chuang Tzu‐Chao1ORCID,Fang Guan‐Shiun1,Hsu Shih‐Chung2,Lee Yi‐Jen3,Shao Wei‐Syun1,Wang Vinchi45,Lee Shou‐Lun6ORCID,Kao Ming‐Ching6,Ou Chien‐Chih7

Affiliation:

1. Department of Chemistry Tamkang University New Taipei Taiwan, R.O.C.

2. Department of Early Childhood Care and Education University of Kang Ning Taipei Taiwan, R.O.C.

3. Department of Biochemistry National Defense Medical Center Taipei Taiwan, R.O.C.

4. Department of Neurology Cardinal Tien Hospital New Taipei Taiwan, R.O.C.

5. School of Medicine, College of Medicine Fu‐Jen Catholic University New Taipei Taiwan, R.O.C.

6. Department of Biological Science and Technology China Medical University Taichung Taiwan, R.O.C.

7. Department of Obstetrics and Gynecology Tri‐Service General Hospital Taipei Taiwan, R.O.C.

Abstract

AbstractThe upregulation of the HER2 oncogene is associated with a variety of human cancers and is associated with poor prognosis. Baicalein is reported to have anti‐tumor activity, but the molecular mechanism of this effect in HER2‐positive cancer cells has not been studied. In this study, our data showed that baicalein can inhibit the proliferation and transformation potential of ovarian cancer cells overexpressing HER2. Baicalein treatment caused a dose‐dependent inhibition of HER2 gene expression at the transcriptional level. Baicalein acted on ovarian cancer cells overexpressing HER2 to downregulate the PI3K/Akt signaling pathway downstream of HER2 and inhibit the expression or activity of downstream targets, such as VEGF and cyclin D1 and MMP2. Oral administration of baicalein supplemented with a pharmaceutical excipient significantly inhibited the growth of HER2‐overexpressing ovarian SKOV‐3 cancer xenografts in mice. These results suggest that downregulation of HER2 gene expression by baicalein at the transcriptional level contributes to inhibit the in vitro and in vivo proliferation and HER2‐mediated malignant transformation of HER2‐overexpressing ovarian cancer cells.

Funder

Ministry of Science and Technology, Taiwan

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Management, Monitoring, Policy and Law,Toxicology,General Medicine

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