Evidence map›Paper›PMID 36474147›Full record

ArticleCellular & molecular biology letters2022

Exosomal miR-628-5p from M1 polarized macrophages hinders m6A modification of circFUT8 to suppress hepatocellular carcinoma progression.

Liyan Wang, Xiaoyuan Yi, Xuhua Xiao, Qinghua Zheng, Lei Ma, Bin Li

Open access · goldAbstract read
In one paragraph

Article in Cellular & molecular biology letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

66 citing papers in PubMed, 132 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Tanshinone IIA Restrains Hepatocellular Carcinoma Progression by Regulating METTL3-Mediated m6A Modification of TRIB3 mRNA.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
  20. Article

6 more citing papers are in PubMed but not listed here.

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.

Liyan WangDigestive Department, Affiliated Hospital of Guilin Medical College, No.15 Lequn Road, Xiufeng District, Guilin, 541001, Guangxi, China.
Xiaoyuan YiDigestive Department, Affiliated Hospital of Guilin Medical College, No.15 Lequn Road, Xiufeng District, Guilin, 541001, Guangxi, China.
Xuhua XiaoDigestive Department, Affiliated Hospital of Guilin Medical College, No.15 Lequn Road, Xiufeng District, Guilin, 541001, Guangxi, China.
Qinghua ZhengDigestive Department, Affiliated Hospital of Guilin Medical College, No.15 Lequn Road, Xiufeng District, Guilin, 541001, Guangxi, China.
Lei MaDigestive Department, Affiliated Hospital of Guilin Medical College, No.15 Lequn Road, Xiufeng District, Guilin, 541001, Guangxi, China.
Bin LiDigestive Department, Affiliated Hospital of Guilin Medical College, No.15 Lequn Road, Xiufeng District, Guilin, 541001, Guangxi, China. Leebien@163.com.
Affiliated Hospital of Guilin Medical College · CN

Funding

Guangxi Zhuang Autonomous Region Health and Family Planning Commission No. S201407-04
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is the most common type of liver cancer. CircFUT8 has been shown to be upregulated in cancers, but its function in HCC remains unclear. Tumor-associated macrophages (TAMs) are one of the main components of the tumor microenvironment (TME), and M1 macrophages function as tumor suppressors in cancers. Exosomes exert an important role in the TME, and circRNAs can be modified by m6A. We investigated the function of circFUT8 in HCC and its interaction with exosomes, M1 macrophages, and m6A.

methodsCircFUT8 expression was detected in HCC cells, and its effects on HCC cell growth were verified through functional assays. Mechanism assays including RNA pull down, RNA-binding protein immunoprecipitation (RIP), and luciferase reporter assays were undertaken to verify how circFUT8 may interact with miR-628-5p, and how these molecules may modulate HCC cell malignancy via interacting with exosomes and macrophages.

resultsCircFUT8 was upregulated in HCC cells and it accelerated HCC cell growth. Exosomes derived from M1 macrophages transferred miR-628-5p to HCC cells to inhibit human methyltransferase-like 14 (METTL14) expression. METTL14 promoted circFUT8 m6A modification and facilitated its nuclear export to the cytoplasm, where M1 macrophages regulated the circFUT8/miR-552-3p/CHMP4B pathway, thereby suppressing HCC progression.

conclusionM1 macrophages-derived exosomal miR-628-5p inhibited the m6A modification of circFUT8, inhibiting HCC development.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMicroRNAsHumansTumor MicroenvironmentMicroRNAsMIRN552 microRNA, humanMIRN628 microRNA, humancircFUT8ExosomesHepatocellular carcinomaM1 macrophagesm6A modification

Identifiers

PMID36474147
PMCPMC9724320
OpenAlexW4310871679

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.