The heterogeneity of plasma miRNA profiles in hepatocellular carcinoma patients and the exploration of diagnostic circulating miRNAs for hepatocellular carcinoma

被引:16
作者
Bai, Xue [1 ]
Liu, Zhenzhen [1 ]
Shao, Xiaojian [1 ,5 ]
Wang, Di [1 ,6 ]
Dong, Encheng [1 ]
Wang, Yan [3 ]
Wu, Chung-I [1 ]
Yuan, Yunfei [2 ]
Lu, Xuemei [1 ,4 ]
Li, Chunyan [1 ]
机构
[1] Chinese Acad Sci, Beijing Inst Genom, Key Lab Genom & Precis Med, Beijing, Peoples R China
[2] Sun Yat Sen Univ, Canc Ctr, Dept Hepatobiliary Oncol, Key Lab Oncol South China, Guangzhou, Guangdong, Peoples R China
[3] Capital Med Univ, Beijing Anzhen Hosp, Beijing, Peoples R China
[4] Chinese Acad Sci, Ctr Excellence Anim Evolut & Genet, Kunming, Yunnan, Peoples R China
[5] Natl Res Council Canada, Digital Technol, Ottawa, ON, Canada
[6] Peking Univ, Acad Adv Interdisciplinary Studies, Peking Tsinghua Ctr Life Sci, Beijing, Peoples R China
关键词
CANCER-CELLS; INTRATUMOR HETEROGENEITY; ALPHA-FETOPROTEIN; TUMOR-SUPPRESSOR; MICRORNAS; EVOLUTION; PROLIFERATION; EXPRESSION; GROWTH;
D O I
10.1371/journal.pone.0211581
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
Heterogeneity is prevalent in cancer both between and within individuals. Although a few studies have identified several circulating microRNAs (miRNAs) for cancer diagnosis, the complete plasma miRNA profile for hepatocellular carcinoma (HCC) remains undefined, and whether the plasma miRNA profiles are heterogeneous is unknown. Here, we obtained individualized plasma miRNA profiles of both healthy subjects and HCC patients via genome-wide deep sequencing. Compared with the highly stable miRNA profile of the healthy subjects, the profile of the HCC patients was highly variable. Seven miRNAs were optimized as potential plasma-based biomarkers for HCC diagnosis. Combined with the clinical data of The Cancer Genome Atlas (TCGA) cohort, three out of the seven miRNAs were correlated with the survival of the HCC patients. To investigate the effect of cancer cells on the plasma miRNAs profile, we compared the most differentially expressed miRNAs between plasma and tissues. Furthermore, miRNAseq data of HCC patients from TCGA were recruited for comparisons. We found that the differences between plasma and tissue were inconsistent, suggesting that other cells in addition to cancer cells also contribute to plasma miRNAs. Using two HCC cancer cell lines, we examined the levels of seven differentially expressed miRNAs. The reverse direction of certain miRNAs alterations between cancer cells and media further confirmed that miRNAs may be selectively pump out by cancer cells.
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页数:15
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