1. Academic Validation
  2. AGR3 promotes estrogen receptor-positive breast cancer cell proliferation in an estrogen-dependent manner

AGR3 promotes estrogen receptor-positive breast cancer cell proliferation in an estrogen-dependent manner

  • Oncol Lett. 2020 Aug;20(2):1441-1451. doi: 10.3892/ol.2020.11683.
Lei Jian 1 2 Jian Xie 3 Shipeng Guo 1 2 Haochen Yu 1 Rui Chen 1 Kai Tao 4 Chengcheng Yang 1 Kang Li 1 2 Shengchun Liu 1
Affiliations

Affiliations

  • 1 Department of Endocrine Breast Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P.R. China.
  • 2 Ministry of Education Key Laboratory of Child Development and Disorders and Chongqing Key Laboratory of Translational Medical Research in Cognitive Development and Learning and Memory Disorders, Children's Hospital of Chongqing Medical University, Chongqing 400016, P.R. China.
  • 3 Department of General Surgery, Yong Chuan Hospital of Chongqing Medical University, Chongqing 402160, P.R. China.
  • 4 The Second Department of Gynecologic Oncology, Shaanxi Provincial Tumor Hospital, The Affiliated Hospital of Medical College of Xi'an Jiao Tong University, Xi'an, Shaanxi 710061, P.R. China.
Abstract

Breast Cancer is one of the most common malignancies and the leading cause of cancer-associated death among women. Anterior gradient 3 (AGR3) is a cancer-associated gene and is similar to its homologous oncogene AGR2. However, whether AGR3 participates in breast Cancer progression remains unclear. The present study aimed to investigate the function of AGR3 in ER-positive breast Cancer. In the present study, reverse transcription-quantitative PCR was used to detect AGR3 mRNA expression in breast Cancer tissues and cell lines; linear correlation analysis was used to investigate the correlation between AGR3 and Estrogen Receptor 1 (ESR1) expression in breast Cancer via GEO dataset analysis; western blotting was used to assess the levels of AGR3, ER and GAPDH; small interfering (si)RNA transfection was used to knock down AGR3 and ESR1 expression; and finally the Cell Counting Kit-8 assay was used to evaluate cell viability. In the present study, AGR3 expression was markedly increased in Estrogen Receptor (ER)-positive breast Cancer tissues and cell lines compared with that in ER-negative breast Cancer. AGR3 expression was upregulated in estrogen-treated T47D cells, whereas 4-hydroxytamoxifen, an inhibitor of estrogen-ER activity in breast Cancer cells, downregulated AGR3 expression in T47D cells. Functional assays demonstrated that knockdown of AGR3 using siRNAs inhibited T47D cell proliferation compared with that of the negative control group. Additionally, AGR3 expression was decreased after knocking down ESR1. The present results suggested that AGR3 may serve an important role in estrogen-mediated cell proliferation in breast Cancer and that AGR3 knockdown may be a potential therapeutic strategy for ER-positive breast Cancer.

Keywords

anterior gradient 3; estrogen; estrogen receptor-positive breast cancer; proliferation.

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