Identification of Recurrence-Related microRNAs from Bone Marrow in Hepatocellular Carcinoma Patients

被引:5
|
作者
Sugimachi, Keishi [1 ,2 ]
Sakimura, Shotaro [1 ]
Tomokuni, Akira [3 ]
Uchi, Ryutaro [1 ]
Hirata, Hidenari [1 ]
Komatsu, Hisateru [1 ]
Shinden, Yoshiaki [1 ]
Iguchi, Tomohiro [1 ]
Eguchi, Hidetoshi [1 ,3 ]
Masuda, Takaaki [1 ]
Morita, Kazutoyo [2 ]
Shirabe, Ken [4 ]
Eguchi, Hidetoshi [1 ,3 ]
Maehara, Yoshihiko [4 ]
Mori, Masaki [3 ]
Mimori, Koshi [1 ]
机构
[1] Kyushu Univ, Beppu Hosp, Dept Surg, 4546 Tsurumihara, Beppu, Oita 8740838, Japan
[2] Fukuoka City Hosp, Dept Surg, Fukuoka 8120046, Japan
[3] Osaka Univ, Grad Sch Med, Dept Surg Gastroenterol, Suita, Osaka 5650871, Japan
[4] Kyushu Univ Maidashi, Dept Surg & Sci, Grad Sch Med Sci, Higashi Ku, Fukuoka 8128582, Japan
来源
JOURNAL OF CLINICAL MEDICINE | 2015年 / 4卷 / 08期
基金
日本学术振兴会;
关键词
bone marrow; microRNA; hepatocellular carcinoma; recurrence; BREAST-CANCER; PROMOTES PROLIFERATION; CLINICAL-SIGNIFICANCE; COLORECTAL-CANCER; DOWN-REGULATION; CELLS; EXPRESSION; EXOSOMES; APOPTOSIS; BIOMARKER;
D O I
10.3390/jcm4081600
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hepatocellular carcinoma (HCC) is a poor-prognosis cancer due to its high rate of recurrence. microRNAs (miRNAs) are a class of small non-coding RNA molecules that affect crucial processes in cancer development. The objective of this study is to identify the role of miRNAs in patient bone marrow (BM) and explore the function of these molecules during HCC progression. We purified miRNAs from bone marrow cells of seven HCC patients, and divided them into three fractions by cell surface markers as follows: CD14(+) (macrophage), CD14(-)/CD45(+) (lymphocyte), and CD14(-)/CD45(-)/EpCAM(+) (epithelial cell). We employed microarray-based profiling to analyze miRNA expression in the bone marrow of patients with HCC. Differentially expressed miRNAs were significantly different between fractions from whole bone marrow, macrophages, and lymphocytes, and depended on stages in tumor progression. Differences in expression of miRNAs associated with cell proliferation also varied significantly between HCC patients with recurrence, multiple tumors, and advanced clinical stages. These results suggest that miRNA profiles in separated fractions of BM cells are associated with HCC progression.
引用
收藏
页码:1600 / 1611
页数:12
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