miRNA profiling reveals a potential role of milk stasis in breast carcinogenesis

被引:29
作者
Gu, Yi-Qi [1 ]
Gong, Gu [1 ]
Xu, Zhe-Li [1 ]
Wang, Li-Ying [2 ]
Fang, Ming-Li [2 ]
Zhou, Hui [1 ]
Xing, Hua [1 ]
Wang, Ke-Ren [1 ]
Sun, Liang [1 ]
机构
[1] Jilin Univ, China Japan Union Hosp, Changchun 130033, Jilin, Peoples R China
[2] Jilin Univ, Coll Basic Med Sci, Dept Mol Biol, Changchun 130021, Jilin, Peoples R China
关键词
milk stasis; miRNA; miRNA profile; breast cancer; biomarker; IMMUNE-RELATED MICRORNAS; RISK-FACTOR; MAMMARY-GLAND; TUMOR MICROENVIRONMENT; CANCER; METASTASIS; NUTRIENTS; ABUNDANT;
D O I
10.3892/ijmm.2014.1677
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
The tumor microenvironment plays an important role in breast carcinogenesis. Milk acts as an important microenvironment of breast cancer, but its role in breast carcinogenesis is largely unknown. Milk stasis may exist in the breast for a number of years after breastfeeding. In the present study, we reported the first microRNA (miRNA) profiling of milk from patients with milk stasis. We identified 266 known miRNAs and 271 novel miRNAs in 10 milk stasis only samples, 271 known miRNAs and 140 novel miRNAs in 10 milk stasis plus breast neoplasm samples by deep sequencing. miRNA profiles were different between the two groups. Furthermore, nine tumor suppressor miRNAs such as miR-29a, miR-146 and miR-223 were significantly downregulated, while seven oncogenic miRNAs such as miR-451, miR-486, miR-107, miR-92 and miR-10 were significantly upregulated in the milk of milk stasis plus neoplasm patients. Three of the identified miRNAs (miR-140, miR-21 and let-7a) were selected using real-time PCR, confirming that these miRNAs were highly expressed. The results also showed that the three miRNAs detected were more abundant in the milk than in the blood. In summary, the data suggested that miRNAs in milk from milk stasis patients may contribute to breast carcinogenesis and that they are more sensitive biomarkers for breast cancer than miRNAs in the blood.
引用
收藏
页码:1243 / 1249
页数:7
相关论文
共 36 条
[1]
Inflammatory Breast Diseases during Lactation: Milk Stasis, Puerperal Mastitis, Abscesses of the Breast, and Malignant Tumors - Current and Evidence-Based Strategies for Diagnosis and Therapy [J].
Abou-Dakn, Michael ;
Richardt, Anna ;
Schaefer-Graf, Ute ;
Woeckel, Achim .
BREAST CARE, 2010, 5 (01) :33-37
[2]
The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[3]
MicroRNA-200 Family Modulation in Distinct Breast Cancer Phenotypes [J].
Angeles Castilla, Maria ;
Diaz-Martin, Juan ;
Sarrio, David ;
Romero-Perez, Laura ;
Angeles Lopez-Garcia, Maria ;
Vieites, Begona ;
Biscuola, Michele ;
Ramiro-Fuentes, Susana ;
Isacke, Clare M. ;
Palacios, Jose .
PLOS ONE, 2012, 7 (10)
[4]
Tumor microenvironment and breast cancer progression A complex scenario [J].
Artacho-Cordon, Antonia ;
Artacho-Cordon, Francisco ;
Rios-Arrabal, Sandra ;
Calvente, Irene ;
Isabel Nunez, Maria .
CANCER BIOLOGY & THERAPY, 2012, 13 (01) :14-24
[5]
Human Milk Composition Nutrients and Bioactive Factors [J].
Ballard, Olivia ;
Morrow, Ardythe L. .
PEDIATRIC CLINICS OF NORTH AMERICA, 2013, 60 (01) :49-+
[6]
MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[7]
Benson JR, 2012, FUTURE ONCOL, V8, P697, DOI [10.2217/FON.12.61, 10.2217/fon.12.61]
[8]
Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50 302 women with breast cancer and 96 973 women without the disease [J].
Beral, V ;
Bull, D ;
Doll, R ;
Peto, R ;
Reeves, G ;
La Vecchia, C ;
Magnusson, C ;
Miller, T ;
Peterson, B ;
Pike, M ;
Thomas, D ;
van Leeuwen, F .
LANCET, 2002, 360 (9328) :187-195
[9]
Obesity as a risk factor for development and poor prognosis of breast cancer [J].
Carmichael, A. R. .
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2006, 113 (10) :1160-1166
[10]
Castañeda CA, 2011, EXPERT REV ANTICANC, V11, P1265, DOI [10.1586/era.11.40, 10.1586/ERA.11.40]