Evidence map›Paper›PMID 36133813›Full record

ArticleFrontiers in pharmacology2022

Network pharmacology and

Xu Cao, Hening Chen, Zhiguo Li, Xiaoke Li, Xianzhao Yang, Qiushuo Jin, Yijun Liang, Jiaxin Zhang, Meiyue Zhou, Ningyi Zhang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
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

14 authors at 3 institutions in 1 country.

Xu CaoDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Hening ChenDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Zhiguo LiBeijing Fengtai Hospital of Integrated Traditional and Western Medicine, Beijing, China.
Xiaoke LiDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Xianzhao YangDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Qiushuo JinDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yijun LiangDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Jiaxin ZhangDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Meiyue ZhouDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Ningyi ZhangDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Guang ChenDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Hongbo DuDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Xiaobin ZaoDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yong'an YeDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CNBeijing University of Chinese Medicine · CNBeijing Fengtai Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Chinese traditional medicine KangXianYiAi formula (KXYA) is used to treat hepatic disease in the clinic. Here we aim to confirm the therapeutic effects and explore the pharmacological mechanisms of KXYA on hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC). We first collected and analyzed clinical data of 40 chronic hepatitis B (CHB) patients with precancerous liver lesions under KXYA treatment. Then, the cell viability, migration, cell cycle, and apoptosis of HepAD38 cells with KXYA treatment were examined. Next, we performed network pharmacological analysis based on database mining to obtain the key target pathways and genes of KXYA treatment on HBV-related HCC. We finally analyzed the expression of the key genes between normal and HBV-related HCC tissues in databases and measured the mRNA expression of the key genes in HepAD38 cells after KXYA treatment. The KXYA treatment could reduce the liver nodule size of CHB patients, suppress the proliferation and migration capabilities, and promote apoptosis of HepAD38 cells. The key pathways of KXYA on HBV-related HCC were Cancer, Hepatitis B, Viral carcinogenesis, Focal adhesion, and

Indexed as

bioinformaticsHBV-related hepatocellular carcinomaKangXianYiAi formulanetwork pharmacologicaltraditional Chinese medicine

Identifiers

PMID36133813
PMCPMC9483169
OpenAlexW4294605680

What Socratic 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 Socratic graph.