Evidence map›Paper›PMID 34220494›Full record

ArticleFrontiers in pharmacology2021

Berberine Sensitizes Human Hepatoma Cells to Regorafenib via Modulating Expression of Circular RNAs.

Kunyuan Wang, Ganxiang Yu, Jiaen Lin, Zhilei Wang, Qianting Lu, Chengxin Gu, Tao Yang, Shiming Liu, Hui Yang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

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  7. Development of novel 9-Journal of enzyme inhibition and medicinal chemistry · 2022
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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

9 authors at 2 institutions in 1 country.

Kunyuan WangDepartment of Gastroenterology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Ganxiang YuDepartment of Gastroenterology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Jiaen LinDepartment of Gastroenterology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Zhilei WangDepartment of Gastroenterology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Qianting LuDepartment of Gastroenterology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Chengxin GuDepartment of Gastroenterology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Tao YangDepartment of Gastroenterology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Shiming LiuGuangzhou Institute of Cardiovascular Disease, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Hui YangDepartment of Gastroenterology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Second Affiliated Hospital of Guangzhou Medical University · CNGuangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regorafenib resistance is a key limiting factor in the treatment of advanced hepatocellular carcinoma (HCC). Increasing evidence has demonstrated that Berberine (BBR) can synergistically enhance the therapeutic effect of various chemotherapeutic agents. However, the contribution of BBR on regorafenib therapy remains unclear. The purpose of this study was to explore the combined treatment effect of berberine and regorafenib in HCC. We found that BBR enhanced the cytotoxicity of regorafenib in HCC cells. Compared with regorafenib alone, the combined treatment of BBR and regorafenib significantly inhibited the proliferation of HCC cells and induced cellular apoptosis. Meanwhile, the combined treatment group with BBR (10mg/kg/day) and regorafenib (5mg/kg/day) had a dramatic inhibitory effect on the growth of HCC xenograft tumors in nude mice. The increased apoptosis of xenograft tumors was seen in the combined treatment group. Moreover, a comprehensive circular RNA sequencing was performed to identify differentially expressed circRNAs in HCC cells after exposure to 100µM BBR and 5µM regorafenib. The volcano plot and scatter plot analyses revealed that there were 58 up-regulated and 19 down-regulated differentially expressed circRNAs between the combination treatment and control groups. Among them, the expression of hsa_circ_0032029 and hsa_circ_0008928 were up-regulated in HCC cells after treatment with 100µM BBR and 5µM regorafenib. Taken together, this study demonstrated that BBR enhanced the anti-HCC effect of regorafenib both

Indexed as

apoptosisberberinecircular RNAshepatocellular carcinomaproliferationregorafenib

Identifiers

PMID34220494
PMCPMC8248669
OpenAlexW3174278175

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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.