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The effect of miR-381 on proliferation and prognosis of breast cancer by altering CCNA2 expression.
Cao, Ming-Gang; Wang, Yan; Yang, Zhi-Min; Wang, Yang; Wang, Mei-Qing; Zhuo, Shuai; Yang, Yan; Liu, Chun-Sheng.
Affiliation
  • Cao MG; Department of Clinical Medicine, Anhui College of Traditional Chinese Medicine, Wuhu, China.
  • Wang Y; Department of Central Sterile Supply, The Second People's Hospital of Wuhu, Wuhu, China.
  • Yang ZM; Department of Laboratory, The First Affiliated Hospital of Wannan Medical College, Wuhu, China.
  • Wang Y; Department of Clinical Medicine, Anhui College of Traditional Chinese Medicine, Wuhu, China.
  • Wang MQ; Department of Clinical Medicine, Anhui College of Traditional Chinese Medicine, Wuhu, China.
  • Zhuo S; Department of Clinical Medicine, Anhui College of Traditional Chinese Medicine, Wuhu, China.
  • Yang Y; Department of Clinical Medicine, Anhui College of Traditional Chinese Medicine, Wuhu, China.
  • Liu CS; Department of Laboratory, The First Affiliated Hospital of Wannan Medical College, Wuhu, China.
J Obstet Gynaecol ; 44(1): 2360547, 2024 Dec.
Article in En | MEDLINE | ID: mdl-38904638
ABSTRACT

BACKGROUND:

MiR-381 can regulate the expression of cyclin A2 (CCNA2) to inhibit the proliferation and migration of bladder cancer cells, but whether miR-381 has the same function in breast cancer is not well know.

METHODS:

The over express or silence miR-381 expressing cell lines were constructed by lentivirus infection to reveal the biological functions of miR-381 in vitro. The expression of miR-381 and CCNA2 in 162 breast cancer patients were detected to further reveal their impact and predictive value on progression-free survival (PFS) and overall survival (OS).

RESULTS:

After transfection of MDA-MB-231 and MCF-7 cells with miR-381 mimics, the expression of miR-381 was effectively up-regulated and CCNA2 was effectively down-regulated, while the opposite results were observed in tumour cell which transfected with miR-381 inhibitors. After transfection of cell lines with miR-381 mimics, tumour cell activity was significantly reduced, while the opposite results were observed in tumour cell which transfected with miR-381 inhibitors. The area under curves (AUCs) of miRNA-381 and CCNA2 for predicting PFS and OS were 0.711, 0.695, 0.694 and 0.675 respectively. Cox regression analysis showed that miRNA-381 ≥ 1.65 2-ΔΔCt and CCNA ≥ 2.95 2-ΔΔCt were the influence factors of PFS and OS, the hazard ratio (HR) values were 0.553, 2.075, 0.462 and 2.089, respectively.

CONCLUSION:

miR-381 inhibitors breast cancer cells proliferation and migration by down-regulating the expression of CCNA2, both of them can predict the prognosis of breast cancer.
miR-381 can regulate the expression of cyclin A2 and inhibit the proliferation and migration of bladder cancer cells, but whether miR-381 has the same function in breast cancer is not well know. We analysed the levels of miR-381 and cyclin A2 in breast cancer patients and breast cancer cells to reveal the mechanism of miR-381 affecting the expression of cyclin A2. We found miRNA-381 affects the proliferation and migration of breast cancer cells by down-regulating the expression of cyclin A2. The expression of serum miR-381 and cyclin A2 have important values in predicting the prognosis of breast cancer. Our findings provide mechanistic insights into how miR-381 regulates the proliferation and migration of breast cancer, as well as a new target for clinical treatment. Future research may focus on how to improve patient prognosis by up-regulating expression of miR-381 and down-regulating the expression of cyclin A2.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Gene Expression Regulation, Neoplastic / MicroRNAs / Cell Proliferation / Cyclin A2 Limits: Adult / Female / Humans / Middle aged Language: En Journal: J Obstet Gynaecol Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Gene Expression Regulation, Neoplastic / MicroRNAs / Cell Proliferation / Cyclin A2 Limits: Adult / Female / Humans / Middle aged Language: En Journal: J Obstet Gynaecol Year: 2024 Document type: Article Affiliation country:
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