Evidence map›Paper›PMID 27677421›Full record

ArticleScientific reports2016

Potentials of the elevated circulating miR-185 level as a biomarker for early diagnosis of HBV-related liver fibrosis.

Bin-Bin Li, Dong-Liang Li, Chao Chen, Bao-Hai Liu, Chun-Yan Xia, Han-Jun Wu, Chao-Qun Wu, Guo-Qin Ji, Su Liu, Wu Ni and 13 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Quantitative T2 mapping of rats with chronic hepatitis.Experimental and therapeutic medicine · 2021
    Article
  8. Review
  9. Review
  10. Article
  11. siRNA- and miRNA-based therapeutics for liver fibrosis.Translational research : the journal of laboratory and clinical medicine · 2019
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Hepatic stellate cells as key target in liver fibrosis.Advanced drug delivery reviews · 2017
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Bin-Bin LiDepartment of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Dong-Liang LiDepartment of Hepatobiliary Medicine, Fuzhou General Hospital of Nanjing Military Command, Fuzhou 350025, Fujian Province, China.
Chao ChenDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Bao-Hai LiuDepartment of Training, the Second Military Medical University, Shanghai 200433, China.
Chun-Yan XiaDepartment of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Han-Jun WuDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Chao-Qun WuSchool of Life Sciences, Fudan University, Shanghai 200433, P. R. China.
Guo-Qin JiState Key Laboratory of Genetic Engineering, Institute of Genetics, School of Life Sciences, Fudan University, Shanghai 200433, P. R. China.
Su LiuDepartment of Gastroenterology, the Second Military Medical University, Shanghai 200433, China.
Wu NiDepartment of Infectious Diseases, the Second Military Medical University, Shanghai 200433, China.
Ding-Kang YaoDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Zhi-Yu ZengDepartment of Hepatobiliary Medicine, Fuzhou General Hospital of Nanjing Military Command, Fuzhou 350025, Fujian Province, China.
Da-Gui ChenDepartment of Pharmacy, College of Pharmacy, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Bao-Dong QinDepartment of Clinical Laboratory, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Xuan XinDepartment of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Gang-Li YanDepartment of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Dan TangDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Hui-Min LiuDepartment of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Jin HeDepartment of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Hongli YanDepartment of Laboratory Medicine Changhai Hospital, The Second Military Medical University, 168 Changhai Road, Shanghai 200433, P. R. China.
Wei-Jian ZhuDepartment of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Hong-Yu YuDepartment of Pathology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Liang ZhuDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early diagnosis of liver fibrosis is critical for early intervention and prognosis of various chronic liver diseases. Conventional repeated histological assessment is impractical due to the associated invasiveness. In the current study, we evaluated circulating miR-185 as a potential biomarker to predict initiation and progression of liver fibrosis. We found that miR-185 was significantly up-regulated in blood specimens from patients with HBV-liver fibrosis and rats with liver fibrosis, the miR-185 levels were correlated with liver fibrosis progression, but not with the different viral loads in HBV-infected patients. miR-185 was observed in collagen deposition regions during advanced liver fibrosis. We found that differences in miR-185 levels facilitated the discrimination between early-staged or advanced-staged liver fibrosis and the healthy controls with high specificity, sensitivity, and likelihood ratio using receiver-operator characteristic analysis. miR-185 targeted SREBF1, and increased expression of COL1A1 and a-SMA genes that are hallmarks of liver fibrosis. Our data supported that circulating miR-185 levels could be used as potential biomarkers for the early diagnosis of liver fibrosis.

Identifiers

PMID27677421
PMCPMC5039723

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.