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西安交通大学第一附属医院乳腺外科,陕西 西安 710061
纸质出版日期:2024-03-25,
收稿日期:2023-03-28,
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何姣,周瑜辉,马晓霞等.血清miR-155、miR-23b在特发性肉芽肿乳腺炎和乳腺癌中的差异性表达及意义[J].局解手术学杂志,2024,33(03):217-221.
HE Jiao,ZHOU Yu-hui,MA Xiao-xia,et al.Differential expression and significance of serum miR-155 and miR-23b in idiopathic granulomatous mastitis and breast cancer[J].JOURNAL OF REGIONAL ANATOMY AND OPERATIVE SURGERY,2024,33(03):217-221.
何姣,周瑜辉,马晓霞等.血清miR-155、miR-23b在特发性肉芽肿乳腺炎和乳腺癌中的差异性表达及意义[J].局解手术学杂志,2024,33(03):217-221. DOI: 10.11659/jjssx.03E023177.
HE Jiao,ZHOU Yu-hui,MA Xiao-xia,et al.Differential expression and significance of serum miR-155 and miR-23b in idiopathic granulomatous mastitis and breast cancer[J].JOURNAL OF REGIONAL ANATOMY AND OPERATIVE SURGERY,2024,33(03):217-221. DOI: 10.11659/jjssx.03E023177.
目的
2
探讨miR-155、miR-23b在特发性肉芽肿乳腺炎(IGM)和乳腺癌(BC)鉴别诊断中的作用。
方法
2
选取2018年10月至2021年11月我院收治的32例IGM患者(ICM组)和40例BC患者(BC组),所有患者均经活检确诊。另外纳入33例健康女性作为对照组。比较患者的临床资料。采用实时荧光定量PCR检测血清miRNAs表达水平。采用受试者工作特征(
ROC
)曲线评估血清miR-155、miR-23b对IGM和BC的诊断价值。采用
Pearson
相关系数法评估相关性。
结果
2
3组CRP、WBC、Hb、Hct、CA19-9、CA15-3、CA125水平比较,差异有统计学意义(
P
<
0.05)。IGM组患者血清miR-155、miR-16-5p、miR-21-5p、miR-210-3p、miR-222-3p、miR-29c-3p表达水平较对照组升高(
P
<
0.001),血清miR-23b表达水平低于对照组(
P
<
0.001);BC组患者血清中以上miRNAs表达水平均高于对照组(
P
<
0.001)。BC组患者血清miR-155表达水平低于IGM组(
P
<
0.001),血清miR-23b表达水平高于IGM组(
P
<
0.001)。血清miR-155和miR-23b水平鉴别诊断IGM和BC的
ROC
曲线下面积(
AUC
)分别为0.722(95%
CI
:0.601~0.843)、0.765(95%
CI
:0.657~0.874),敏感度分别为81.00%、77.50%,特异度分别为65.00%、59.40%;二者联合鉴别诊断的
AUC
为0.869(95%
CI
:0.786~0.951),敏感度和特异度分别为84.10%和92.50%。IGM组血清miR-155与WBC、CRP水平均呈正相关(
P
<
0.05),而血清miR-23b与WBC、CRP水平均呈负相关(
P
<
0.05)。
结论
2
血清miR-155和miR-23b有助于区分IGM和BC,可成为IGM和BC早期鉴别诊断的靶标。
Objective
2
To investigate the roles of miR-155 and miR-23b in the differential diagnosis of idiopathic granulomatous mastitis (IGM) and breast cancer (BC).
Methods
2
A total of 32 patients with IGM (the ICM group) and 40 patients with BC (the BC group) admitted to our hospital from October 2018 to November 2021 were selected. All patients were confirmed by biopsy. In addition,33 healthy women were included as the control group. The clinical data of patients were compared. The expression levels of serum miRNAs were detected by real-time fluorescence quantitative PCR. The diagnostic value of serum miR-155 and miR-23b for IGM and BC was evaluated by
receiver operating characteristic
(
ROC
) curve.The
Pearson
correlation coefficient method was used to evaluate the correlation.
Results
2
There were statistically significant differences in the levels of CRP
WBC
Hb
Hct
CA19-9
CA15-3 and CA125 among the three groups (
P
<
0.05).The expression levels of serum miR-155,miR-16-5p,miR-21-5p,miR-210-3p,miR-222-3p and miR-29c-3p in the IGM group were higher than those in the control group (
P
<
0.001),and the expression level of serum miR-23b was lower than that in the control group (
P
<
0.001). The expression levels of the above miRNAs of serum in the BC group were higher than those in the control group (
P
<
0.001). The expression level of serum miR-155 in the BC group was lower than that in the IGM group (
P
<
0.001),and the expression level of serum miR-23b was higher than that in the IGM group (
P
<
0.001).The
area under
the
ROC
curve
(
AUC
) for the differential diagnosis of IGM and BC by serum miR-155 and miR-23b levels were 0.722 (95%
CI
:0.601 to 0.843) and 0.765 (95%
CI
:0.657 to 0.874),respectively,with sensitivity of 81.00% and 77.50%,and specificity of 65.00% and 59.40%,respectively.The
AUC
of combined differential diagnosis was 0.869 (95%
CI
:0.786 to 0.951),and the sensitivity and specificity were 84.10% and 92.50%,respectively. Serum miR-155 was positively correlated with WBC and CRP levels in the IGM group (
P
<
0.05),while serum miR-23b was negatively correlated with WBC and CRP levels (
P<
0.05).
Conclusion
2
Serum miR-155 and miR-23b are helpful in distinguishing IGM from BC,and can be used as targets for early differential diagnosis of IGM and BC.
特发性肉芽肿乳腺炎乳腺癌鉴别诊断miR-155miR-23b
idiopathic granulomatous mastitisbreast cancerdifferential diagnosismiR-155miR-23b
鞠仙莉,阎红琳,袁静萍.肉芽肿性小叶性乳腺炎临床病理学研究进展[J].中国组织化学与细胞化学杂志,2022,31(4):407-411.doi:10.16705/j.cnki.1004-1850.2022.04.013http://dx.doi.org/10.16705/j.cnki.1004-1850.2022.04.013.
吕锋.特发性肉芽肿性乳腺炎的诊断及治疗现状[J].济宁医学院学报,2020,43(2):132-136.doi:10.3969/j.issn.1000-9760. 2020.02.014http://dx.doi.org/10.3969/j.issn.1000-9760.2020.02.014.
任宝凤,杨毅.特发性肉芽肿性乳腺炎研究进展[J].吉林医学,2018,39(11):2156-2158.doi:10.3969/j.issn.1004-0412.2018. 11.072http://dx.doi.org/10.3969/j.issn.1004-0412.2018.11.072.
武帅,杨君,郑云.乳腺癌中具有双重功能的miRNA[J].中国临床药理学与治疗学,2022,27(7):814-821.doi:10.12092/j.issn.1009-2501.2022.07.013http://dx.doi.org/10.12092/j.issn.1009-2501.2022.07.013.
王晓刚.miRNA作为乳腺癌无创标志物的研究进展[J].检验医学与临床,2020,17(20):3038-3041.doi:10.3969/j.issn.1672-9455. 2020.20.040http://dx.doi.org/10.3969/j.issn.1672-9455.2020.20.040.
Soleimanpour E,Babaei E,Hosseinpour-Feizi MA,et al.Circulating miR-21 and miR-155 as potential noninvasive biomarkers in Iranian Azeri patients with breast carcinoma[J].J Cancer Res Ther,2019,15(5):1092-1097.doi:10.4103/jcrt.JCRT_1227_16http://dx.doi.org/10.4103/jcrt.JCRT_1227_16.
Wang Z,Hu S,Li X,et al.MiR-16-5p suppresses breast cancer proliferation by targeting ANLN[J].BMC Cancer,2021,21(1):1188-1198.doi:10.1186/s12885-021-08914-1http://dx.doi.org/10.1186/s12885-021-08914-1.
Hannafon BN,Cai A,Calloway CL,et al.miR-23b and miR-27b are oncogenic microRNAs in breast cancer:evidence from a CRISPR/Cas9 deletion study[J].BMC Cancer,2019,19(1):642-652.doi:10.1186/s12885-019-5839-2http://dx.doi.org/10.1186/s12885-019-5839-2.
Li N,Wang X,Sun J,et al.miR-21-5p/Tiam1-mediated glycolysis reprogramming drives breast cancer progression via enhancing PFKL stabilization[J].Carcinogenesis,2022,43(7):705-715.doi:10.1093/carcin/bgac039http://dx.doi.org/10.1093/carcin/bgac039.
Aksan H,Kundaktepe BP,Sayili U,et al.Circulating miR-155,
let-7c,miR-21,and PTEN levels in differential diagnosis and
prognosis of idiopathic granulomatous mastitis and breast cancer[J].Biofactors,2020,46(6):955-962.doi:10.1002/biof.1676http://dx.doi.org/10.1002/biof.1676.
Nashtahosseini Z,Aghamaali MR,Sadeghi F,et al.Circulating status of microRNAs 660-5p and 210-3p in breast cancer patients[J].J Gene Med,2021,23(4):e3320.doi:10.1002/jgm.3320http://dx.doi.org/10.1002/jgm.3320.
Ahmed SH,Espinoza-Sánchez NA,El-Damen A,et al.Small extracellular vesicle-encapsulated miR-181b-5p,miR-222-3p and let-7a-5p:next generation plasma biopsy-based diagnostic biomarkers for inflammatory breast cancer[J].PLoS One,2021,16(4):e0250642.doi:10.1371/journal.pone.0250642http://dx.doi.org/10.1371/journal.pone.0250642.
Kunc M,Popęda M,Niemira M,et al.microRNA expression profile in single hormone receptor-positive breast cancers is mainly dependent on HER2 status-a pilot study[J].Diagnostics (Basel),2020,10(9):617-630.doi:10.3390/diagnostics10090617http://dx.doi.org/10.3390/diagnostics10090617.
Grimaldi AM,Nuzzo S,Condorelli G,et al.Prognostic and clinicopathological significance of miR-155 in breast cancer:a systematic
review[J].Int J Mol Sci,2020,21(16):5834-5845.doi:10.3390/ijms21165834http://dx.doi.org/10.3390/ijms21165834.
Anwar SL,Tanjung DS,Fitria MS,et al.Dynamic changes of
circulating miR-155 expression and the potential application as a non-invasive biomarker in breast cancer[J].Asian Pac J Cancer Prev,2020,21(2):491-497.doi:10.31557/APJCP.2020.21.2.491http://dx.doi.org/10.31557/APJCP.2020.21.2.491.
Khalighfard S,Alizadeh AM,Irani S,et al.Plasma miR-21,miR-155,miR-10b,and Let-7a as the potential biomarkers for the monitoring of breast cancer patients[J].Sci Rep,2018,8(1):17981-17990.doi:10.1038/s41598-018-36321-3http://dx.doi.org/10.1038/s41598-018-36321-3.
Xu WD,Feng SY,Huang AF.Role of miR-155 in inflammatory autoimmune diseases:a comprehensive review[J].Inflamm Res,2022,71(12):1501-1517.doi:10.1007/s00011-022-01643-6http://dx.doi.org/10.1007/s00011-022-01643-6.
Maciak K,Dziedzic A,Miller E,et al.miR-155 as an important regulator of multiple sclerosis pathogenesis.A review[J].Int J Mol Sci,2021,22(9):4332-4346.doi:10.3390/ijms22094332http://dx.doi.org/10.3390/ijms22094332.
Yang B,Yang R,Xu B,et al.miR-155 and miR-146a collectively regulate meningitic Escherichia coli infection-mediated neuroinflammatory responses[J].J Neuroinflammation,2021,18(1):1-19.doi:10.1186/s12974-021-02165-4http://dx.doi.org/10.1186/s12974-021-02165-4.
Zhang ZB,Guo YF,Li CY,et al.Selenium influences mmu-miR-155 to inhibit inflammation in Staphylococcus aureus-induced mastitis in mice[J].Food Funct,2019,10(10):6543-6555.doi:10.1039/c9fo01488hhttp://dx.doi.org/10.1039/c9fo01488h.
Tavasolian F,Hosseini AZ,Soudi S,et al.A systems biology
approach for miRNA-mRNA expression patterns analysis in rheumatoid arthritis[J].Comb Chem High Throughput Screen,2021,24(2):195-212.doi:10.2174/1386207323666200605150024http://dx.doi.org/10.2174/1386207323666200605150024.
Hong SM,Liu C,Yin Z,et al.MicroRNAs in systemic lupus erythematosus:a perspective on the path from biological discoveries to clinical practice[J].Curr Rheumatol Rep,2020,22(6):1-9.doi:10.1007/s11926-020-00895-7http://dx.doi.org/10.1007/s11926-020-00895-7.
Chen L,Liu X,Li Z,et al.Expression differences of miRNAs and genes on NF- κB pathway between the healthy and the mastitis
Chinese Holstein cows[J].Gene,2014,545(1):117-125.doi:10.1016/j.gene.2014.04.071http://dx.doi.org/10.1016/j.gene.2014.04.071.
Papadaki C,Stoupis G,Tsalikis L,et al.Circulating miRNAs as a marker of metastatic disease and prognostic factor in metastatic breast cancer[J].Oncotarget,2019,10(9):966-981.doi:10.18632/oncotarget.26629http://dx.doi.org/10.18632/oncotarget.26629.
Yin Y,Liu X,Meng Q,et al.Idiopathic granulomatous mastitis:etiology,clinical manifestation,diagnosis and treatment[J].J Invest Surg,2022,35(3):709-720.doi:10.1080/08941939.2021.1894516http://dx.doi.org/10.1080/08941939.2021.1894516.
Ling J,Xie X,Wang Y,et al.Differential expression profiles of miRNA in granulomatous lobular mastitis and identification of
possible biomarkers[J].Exp Ther Med,2022,24(2):500-510.doi:10.3892/etm.2022.11427http://dx.doi.org/10.3892/etm.2022.11427.
Zheng B,Song J,Lu M,et al.Current research describing the role of CD4+ T lymphocyte subsets in the pathogenesis of granulomatous
lobular mastitis[J].J Invest Surg,2022,35(10):1790-1795.doi:10.1080/08941939.2022.2090035http://dx.doi.org/10.1080/08941939.2022.2090035.
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