LI Ya′nan1 JIN Chunming2▲ GONG Fangyan2 GAO Yu1 DENG Meng1 ZHANG Hang1 DING Xinzhe1 YIN Guibin1
1. The First School of Clinical Medicine, Mudanjiang Medical University, Heilongjiang Province, Mudanjiang 157000,China;
2. Department of Laboratory Medicine, Hongqi Hospital Affiliated to Mudanjiang Medical University, Heilongjiang Province, Mudanjiang 157000, China
Objective To investigate the effect of microRNA-501-5p(miR-501-5p)in breast cancer.Methods Forty patients with breast cancer diagnosed for the first time in Tumor Hospital of Mudanjiang City from March 2020 to March 2021 were selected as the breast cancer group. Forty physical examination subjects in Hongqi Hospital Affiliated to Mudanjiang Medical University during the same period were selected as the healthy control group. Serum of patients in the two groups was collected, and the expression level of miR-501-5p was detected by real-time fluorescence quantitative PCR (qRT-PCR). The expression of LAMTOR5 in tissues was detected by immunohistochemistry. ROC curve was drawn to analyze the value of serum miR-501-5p, carcinoembryonic antigen (CEA), carbohytrate antigen 153(CA153) and carbohytrate antigen 125 (CA125) in the diagnosis of breast cancer. Results The expression level of miR-501-5p in breast cancer tissue (1.12±0.23) was higher than that in adjacent tissues (0.96±0.15), and the difference was statistically significant (P<0.05). The expression level of miR-501-5p in serum of breast cancer patients (0.96±0.67)was higher than that of healthy controls (0.88±0.12), and the difference was statistically significant (P<0.05). The expression level of miR-501-5p in patients with lymph node metastasis and TNM stage Ⅲand Ⅳwere higher than those in patients with TNM stage Ⅰand Ⅱwithout lymph node metastasis, and the differences were statistically significant (P<0.05). The positive rate of LAMTOR5 expression in breast cancer tissue was higher than that in adjacent tissues, and the difference was statistically significant (P<0.05). The AUC of serum miR-501-5p, CEA, CA153 and CA125 in the diagnosis of breast cancer was 0.663, 0.827, 0.687 and 0.633,respectively, and the AUC of four combined diagnosis of breast cancer was 0.877. Conclusion The expression of miR-501-5p is increased in breast cancer tissues and serum of breast cancer patients,and its expression is related to lymph node metastasis and clinical TNM stage of breast cancer.The positive expression of LAMTOR5 in breast cancer tissues was higher than that in adjacent tissues.The expression of LAMTOR5 was positively correlated with the expression level of miR-501-5p. Combined detection of miR-501-5p, CEA, CA153 and CA125 can improve the diagnostic level of breast cancer.
Bray F,Ferlay J,Soerjomataram I,et al.Global cancer statistics 2018:GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J].CA Cancer J Clin,2018,68(6):394-424.
[2]
Román M,Louro J,Posso M,et al.Breast density,benign breast disease,and risk of breast cancer over time[J].Eur Radiol,2021,31(7):4839-4847.
[4]
Bar-Peled L,Schweitzer LD,Roberto Zoncu,et al.Ragulator is a GEF for the rag GTPases that signal amino acid levels to mTORC1[J].Cell,2012,150(6):1196-1208.
[5]
Li Y,Zhen W,Hui S,et al.HBXIP and LSD1 scaffolded by lncRNA hotair mediate transcriptional activation by c-Myc[J].Cancer Res,2016,76(2):293-304.
[6]
Li H,Qian L,Zhen W,et al.The oncoprotein HBXIP modulates the feedback loop of MDM2/p53 to enhance the growth of breast cancer[J].J.Biol.Chem,2015,290(37):22649-22661.
[7]
Marusawa H,Matsuzawa S,Welsh K,et al.HBXIP functions as a cofactor of survivin in apoptosis suppression[J].EMBO J,2003,22(11):2729-2740.
[8]
Sung H,Ferlay J,Siegel RL,et al.Global Cancer Statistics 2020:GLOBOCANEstimatesofIncidenceandMortalityWorldwide for 36 Cancers in 185 Countries[J].CA Cancer J Clin,2021,71(3):209-249.
[12]
Sanches JGP,Xu Y,Yabasin IB,et al.MiR-501 is upregulated in cervical cancer and promotes cell proliferation,migration and invasion by targeting CYLD[J].Chem Biol Interact,2018,285:85-95.
Li N,Wang Y,Che S,et al.HBXIP over expression as an independent biomarker for cervical cancer[J].Exp Mol Pathol,2017,102(1):133-137.
[19]
Qiu L,Lu F,Zhang L,et al.HBXIP Regulates Gastric Cancer Glucose Metabolism and Malignancy Through PI3K/AKT and p53 Signaling[J].Onco Targets Ther,2020,13:3359-3374.
[20]
Piao JJ,Li N,Wang YX,et al.HBXIP expression in gastric adenocarcinoma predicts poor prognosis[J].Zhonghua Bing Li Xue Za Zhi,2017,46(2):88-92.
[17]
Zheng S,Wu H,Wang F,et al.The oncoprotein HBXIP facilitates metastasis of hepatocellular carcinoma cells by activation of MMP15 expression[J].Cancer Manag Res,2019,11:4529-4540.