Evidence map›Paper›PMID 35352818›Full record

ArticleHistology and histopathology2022

CircRNA circBACH1 facilitates hepatitis B virus replication and hepatoma development by regulating the miR-200a-3p/MAP3K2 axis.

Na Du, Kailin Li, Yu Wang, Bo Song, Xuan Zhou, Shaoqiong Duan

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Article in Histology and histopathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
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

17 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  5. Review
  6. Roles of circRNAs in viral pathogenesis.Frontiers in cellular and infection microbiology · 2025
    Review
  7. Circular RNAs in Liver Diseases.Advances in experimental medicine and biology · 2025
    Review
  8. Article
  9. Review
  10. Roles of circRNAs in regulating the tumor microenvironment.Medical oncology (Northwood, London, England) · 2023
    Review
  11. Review
  12. Review
  13. Article
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  16. Article
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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

6 authors at 1 institution in 1 country.

Na Du *Department of Infectious Disease, Suizhou Central Hospital Affiliated to Hubei Medical College, Suizhou, China.
Kailin Li *Department of Infectious Disease, Suizhou Central Hospital Affiliated to Hubei Medical College, Suizhou, China.
Yu WangDepartment of Cardiology, Suizhou Central Hospital Affiliated to Hubei Medical College, Suizhou, China.
Bo SongDepartment of Infectious Disease, Suizhou Central Hospital Affiliated to Hubei Medical College, Suizhou, China.
Xuan ZhouDepartment of Infectious Disease, Suizhou Central Hospital Affiliated to Hubei Medical College, Suizhou, China.
Shaoqiong DuanDepartment of Infectious Disease, Suizhou Central Hospital Affiliated to Hubei Medical College, Suizhou, China. duanshaoqiong1983@163.com.
Suizhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatitis B virus (HBV) is a top contributor to hepatoma. Circular RNAs (circRNAs) have been elucidated to have a close connection with HBV-induced hepatoma. This study aimed to explore the role of circRNA BTB domain and CNC homolog 1 (circBACH1) in HBV replication and hepatoma progression, as well as the potential mechanistic pathway.

methodsQuantitative real-time polymerase chain reaction (qRT-PCR) assay was performed to assess the expression of circBACH1, microRNA (miR)-200a-3p, and mitogen-activated protein kinase kinase kinase 2 (MAP3K2). HBV replication was determined by enzyme-linked immunosorbent assay (ELISA) and qRT-PCR assay. Cell viability and clonogenicity were detected via Cell Counting Kit-8 (CCK-8) assay and colony formation assay, respectively. Cell metastasis was examined by Transwell assay and wound healing assay. Annexing-V/PI staining was employed to monitor cell apoptosis using flow cytometry. Levels of MAP3K2, proliferation- and apoptosis-related proteins were analyzed by Western blotting. Target interaction between miR-200a-3p and circBACH1 or MAP3K2 was confirmed by dual-luciferase reporter assay and RNA immunoprecipitation (RIP) assay. The role of circBACH1 in vivo was investigated by xenograft model assay.

resultsExpression of circBACH1 and MAP3K2 was increased, while miR-200a-3p expression was decreased in HCC tissues and HBV-transfected hepatoma cells. Depletion of circBACH1 or miR-200a-3p overexpression impeded HBV replication, proliferation, and metastasis in HBV-transfected hepatoma cells. CircBACH1 was able to regulate MAP3K2 expression by sponging miR-200a-3p. CircBACH1 regulated HBV replication and hepatoma progression through the miR-200a-3p/MAP3K2 pathway. Moreover, circBACH1 deficiency hampered tumor growth in vivo.

conclusionCircBACH1 knockdown had inhibitory effects on HBV replication and hepatoma progression, at least partly by modulating the miR-200a-3p/MAP3K2 axis.

Indexed as

Carcinoma, HepatocellularHepatitis BLiver NeoplasmsMAP Kinase Kinase Kinase 2MicroRNAsRNA, CircularBasic-Leucine Zipper Transcription FactorsCell Line, TumorCell ProliferationHepatitis B virusHumansVirus ReplicationBACH1 protein, humanBasic-Leucine Zipper Transcription FactorsMAP3K2 protein, humanMAP Kinase Kinase Kinase 2MicroRNAsMIRN200 microRNA, humanRNA, Circular

Identifiers

PMID35352818
OpenAlexW4220708971

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Registered trials

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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.