4.6 Article

Clinical aspects of circulating miRNA-335 in breast cancer patients: A prospective study

期刊

JOURNAL OF CELLULAR BIOCHEMISTRY
卷 120, 期 6, 页码 8975-8982

出版社

WILEY
DOI: 10.1002/jcb.28168

关键词

breast cancer subtypes; clinicopathological factors; diagnosis; micro-RNA; prognosis; tumor suppressor

资金

  1. Science Technology Development Fund (STDF) through Basic and Applied Research Support Grant Project, Egypt [15089]
  2. Science Technology Development Fund (STDF) through Capacity Building Grant Fund, Egypt [4940]

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BackgroundThe impact of aberrant expression of miRNAs, small noncoding RNAs of 19 to 23 nucleotide, has been reported in different types of cancer, such as breast cancer. Authors aim to investigate the role of circulating miRNA-335 as a diagnostic and prognostic marker for breast cancer. Materials and MethodsmiRNA-335 expression was measured in primary breast cancer patients (n=106), patients with benign breast lesion (n=49) and healthy individuals as control (n=40) using quantitative real-time polymerase chain reaction and its diagnostic efficacy, relation with clinicopathological factors, and disease-free survival (DFS) and overall survival (OS) were assessed. ResultsA significant decrease in miRNA-335 expression was reported in patients with breast cancer as compared to the other two investigated groups. The positivity rate for miRNA were related to adverse clinical features of primary breast cancer as high histological grading (X-2=7.72, P=0.016), presence of metastasis to lymph node (X-2=21.8, P<0.001), large tumor size (X-2=6.41, P=0.041), and hormonal status (P<0.001). miRNA-335 mean rank level was significantly different among breast cancer subtypes and its level was inferior in triple negative breast cancer. Worse DFS (X-2=7.76, P=0.005) and OS (X-2=9.3, P=0.002) were reported with decreased miRNA-335 level. ConclusionAssessment of circulating miRNA expression level is a promising minimal invasive marker for diagnosis and prediction of breast cancer prognosis with significant discrepancies among molecular breast cancer subtypes.

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