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Expression of Egl nine homolog 3 in breast cancer and its effect on malignant phenotype of breast cancer cells |
WANG Yang1 ZHAO Zitong2 SONG Yongmei2 ZHANG Bailin1 |
1.Department of Breast Surgery, National Cancer Center National Clinical Research Center for Cancer Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China;
2.State Key Laboratory of Molecular Oncology, National Cancer Center National Clinical Research Center for Cancer Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China |
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Abstract Objective To investigate the expression and function of the Egl nine homolog 3 (EGLN3) in breast cancer. Methods The expression of EGLN3 in 1085 cases of breast cancer tissues and 291 cases of normal tissues from the TCGA and GTEx databases was analyzed by using GEPIA website. A total of 52 cases of breast cancer tissues and adjacent tissues were collected in Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College from January 2010 to December 2017. The EGLN3 mRNA expression in breast cancer tissues was detected by real-time PCR. EGLN3 protein expression in normal breast epithelial cell (MCF-10A) and 11 cell lines of breast cancer (ZR-75-1, SK-BR-3, MDA-MB-453, BT474, MCF-7, T47D, MDA-MB-231, CAL-51, HS578T, MDA-MB-468, HCC1937) were detected by Western blot. The effect of transfection siRNA knockdown EGLN3 on proliferation, clonal formation, invasion and migration of breast cancer cells were detected by xCELLigence RTCA MP system, clonal formation assay and Transwell assay, respectively. Results The expression of EGLN3 mRNA in breast cancer tissues was higher than that in normal tissues, and the difference was statistically significant (P < 0.05). The expression of EGLN3 mRNA in breast cancer tissues was higher than that in adjacent tissues, and the difference was highly statistically significant (P < 0.01). EGLN3 protein was highly expressed in breast cancer cells MDA-MB-231, CAL-51, MDA-MB-468, and HCC1937, but not in normal breast epithelial cells and other breast cancer cells. After transfection with siRNA knockdown EGLN3, the proliferation, clonal formation, invasion and migration of breast cancer cells were decreased. Conclusion EGLN3 expression may be related to the occurrence and development of breast cancer, and down-regulation of EGLN3 can inhibit the malignant phenotype of breast cancer cells, but its mechanism needs further study.
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