Cell-free fetal nucleic acids in amniotic fluid

被引:42
|
作者
Hui, L. [1 ,2 ]
Bianchi, D. W. [1 ]
机构
[1] Tufts Med Ctr, Mother Infant Res Inst, Boston, MA 02111 USA
[2] Univ Sydney, Dept Obstet & Gynaecol, Sydney, NSW 2006, Australia
关键词
amniotic fluid; cell-free fetal nucleic acids; prenatal diagnosis; gene expression; NONINVASIVE PRENATAL-DIAGNOSIS; GENE-EXPRESSION ANALYSIS; FREE MESSENGER-RNA; MATERNAL BODY-FLUIDS; REAL-TIME PCR; FREE DNA; PREGNANT-WOMEN; DOWN-SYNDROME; MICROARRAY ANALYSIS; OXIDATIVE STRESS;
D O I
10.1093/humupd/dmq049
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Research into cell-free fetal (cff) nucleic acids has primarily focused on maternal plasma; however, cff DNA and RNA are also detectable in other body fluids such as amniotic fluid (AF). In AF, cff DNA is present in much greater concentrations than in maternal plasma and represents a pure fetal sample uncontaminated by maternal-and trophoblast-derived nucleic acids. The aim of this review was to summarize the current knowledge on cff nucleic acids in AF and to outline future research directions. METHODS: MEDLINE and PREMEDLINE were searched up to August 2010 for original investigations of cell-free RNA or DNA in AF. Sixteen studies were included in the review. RESULTS: AF cff DNA represents a physiologically separate pool from cff DNA in maternal plasma. The placenta is not a major source of nucleic acids in AF. It is feasible to isolate cff nucleic acids from small volumes of discarded AF supernatant in sufficient quality and quantity to perform microarray studies and downstream applications such as pathway analysis. This 'discovery-driven approach' has resulted in new information on the pathogenesis of Down syndrome and polyhydramnios. There is otherwise a paucity of information relating to the basic biology and clinical applications of cff nucleic acids in AF. CONCLUSIONS: AF supernatant is a valuable and widely available but under-utilized biological resource. Further studies of cff nucleic acids in AF may lead to new insights into human fetal development and ultimately new approaches to antenatal treatment of human disease.
引用
收藏
页码:362 / 371
页数:10
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