Selective Release of MicroRNA Species from Normal and Malignant Mammary Epithelial Cells

被引:479
作者
Pigati, Lucy [1 ]
Yaddanapudi, Sree C. S. [2 ,3 ]
Iyengar, Ravi [1 ]
Kim, Dong-Ja [1 ]
Hearn, Steven A. [4 ]
Danforth, David [5 ]
Hastings, Michelle L. [2 ]
Duelli, Dominik M. [1 ,2 ]
机构
[1] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, Dept Pathol, N Chicago, IL 60064 USA
[2] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, Dept Cell Biol & Anat, N Chicago, IL USA
[3] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, Bligh Canc Res Ctr, N Chicago, IL USA
[4] Cold Spring Harbor Lab, Microscopy Facil, Cold Spring Harbor, NY 11724 USA
[5] NCI, Surg Branch, CCR, NIH, Bethesda, MD 20892 USA
来源
PLOS ONE | 2010年 / 5卷 / 10期
关键词
BREAST-CANCER; GENE-EXPRESSION; STEM-CELLS; CIRCULATING MICRORNAS; TAMOXIFEN RESISTANCE; TUMOR INVASION; MIR-200; FAMILY; MESSENGER-RNA; DUCTAL LAVAGE; EXOSOMES;
D O I
10.1371/journal.pone.0013515
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) in body fluids are candidate diagnostics for a variety of conditions and diseases, including breast cancer. One premise for using extracellular miRNAs to diagnose disease is the notion that the abundance of the miRNAs in body fluids reflects their abundance in the abnormal cells causing the disease. As a result, the search for such diagnostics in body fluids has focused on miRNAs that are abundant in the cells of origin. Here we report that released miRNAs do not necessarily reflect the abundance of miRNA in the cell of origin. We find that release of miRNAs from cells into blood, milk and ductal fluids is selective and that the selection of released miRNAs may correlate with malignancy. In particular, the bulk of miR-451 and miR-1246 produced by malignant mammary epithelial cells was released, but the majority of these miRNAs produced by non-malignant mammary epithelial cells was retained. Our findings suggest the existence of a cellular selection mechanism for miRNA release and indicate that the extracellular and cellular miRNA profiles differ. This selective release of miRNAs is an important consideration for the identification of circulating miRNAs as biomarkers of disease.
引用
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页数:13
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共 106 条
[11]   Detection and characterization of placental MicroRNAs in maternal plasma [J].
Chim, Stephen S. C. ;
Shing, Tristan K. F. ;
Hung, Emily C. W. ;
Leung, Tak-yeung ;
Lau, Tze-kin ;
Chiu, Rossa W. K. ;
Lo, Y. M. Dennis .
CLINICAL CHEMISTRY, 2008, 54 (03) :482-490
[12]   A Novel miRNA Processing Pathway Independent of Dicer Requires Argonaute2 Catalytic Activity [J].
Cifuentes, Daniel ;
Xue, Huiling ;
Taylor, David W. ;
Patnode, Heather ;
Mishima, Yuichiro ;
Cheloufi, Sihem ;
Ma, Enbo ;
Mane, Shrikant ;
Hannon, Gregory J. ;
Lawson, Nathan D. ;
Wolfe, Scot A. ;
Giraldez, Antonio J. .
SCIENCE, 2010, 328 (5986) :1694-1698
[13]   Relative quantification of mRNA: comparison of methods currently used for real-time PCR data analysis [J].
Cikos, Stefan ;
Bukovska, Alexandra ;
Koppel, Juraj .
BMC MOLECULAR BIOLOGY, 2007, 8
[14]   Loss of miR-200c: A Marker of Aggressiveness and Chemoresistance in Female Reproductive Cancers [J].
Cochrane, Dawn R. ;
Howe, Erin N. ;
Spoelstra, Nicole S. ;
Richer, Jennifer K. .
JOURNAL OF ONCOLOGY, 2010, 2010
[15]   CD45 immunoaffinity depletion of vesicles from Jurkat T cells demonstrates that exosomes contain CD45: no evidence for a distinct exosome/HIV-I budding pathway [J].
Coren, Lori V. ;
Shatzer, Teresa ;
Ott, David E. .
RETROVIROLOGY, 2008, 5 (1)
[16]   Combined breast ductal lavage and ductal endoscopy for the evaluation of the high-risk breast: A feasibility study [J].
Danforth, David N., Jr. ;
Abati, Andrea ;
Filie, Armando ;
Prindiville, Shiela A. ;
Palmieri, Diane ;
Simon, Richard ;
Ried, Thomas ;
Steeg, Patricia S. .
JOURNAL OF SURGICAL ONCOLOGY, 2006, 94 (07) :555-564
[17]   Identification of suitable endogenous control genes for microRNA gene expression analysis in human breast cancer [J].
Davoren, Pamela A. ;
McNeill, Roisin E. ;
Lowery, Aoife J. ;
Kerin, Michael J. ;
Miller, Nicola .
BMC MOLECULAR BIOLOGY, 2008, 9
[18]   Morphogenesis and oncogenesis of MCF-10A mammary epithelial acini grown in three-dimensional basement membrane cultures [J].
Debnath, J ;
Muthuswamy, SK ;
Brugge, JS .
METHODS, 2003, 30 (03) :256-268
[19]   The intraductal approach to breast cancer biomarker discovery [J].
Dua, RS ;
Isacke, CM ;
Gui, GPH .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (07) :1209-1216
[20]   A primate virus generates transformed human cells by fusion [J].
Duelli, DM ;
Hearn, S ;
Myers, MP ;
Lazebnik, Y .
JOURNAL OF CELL BIOLOGY, 2005, 171 (03) :493-503