Evidence map›Paper›PMID 40384866›Full record

ArticleInternational journal of biological sciences2025

SRGN-mediated reactivation of the YAP/CRISPLD2 axis promotes aggressiveness of hepatocellular carcinoma.

Shuqiao Zhang, Hao Hu, Xinyu Li, Qiuxia Chen, Yilu Zheng, Huiting Peng, Zhuomao Mo, Wanting Hu, Yantao Li, Senkai Hong and 4 more

Abstract read
In one paragraph

Article in International journal of biological sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Curcumin Targets Crispld2 to Suppress Hepatic Stellate Cell Activation via PI3K/AKT Pathway Inhibition in Hepatic Fibrosis.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  2. Article
  3. 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.

Shuqiao ZhangFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Hao HuFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Xinyu LiFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Qiuxia ChenDepartment of Traditional Chinese Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Yilu ZhengDepartment of Hematology, The Seventh Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Huiting PengFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Zhuomao MoZhejiang University Medical Center, Zhejiang University, Hangzhou, Zhejiang, China.
Wanting HuObstetrics & Gynecology Hospital of Fudan University, Fudan University, Shanghai, China.
Yantao LiFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Senkai HongFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Bijun HuangSun Yat-sen University Cancer Center, Sun Yat-sen University Affiliated Tumor Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Weihong KuangFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Shijun ZhangDepartment of Traditional Chinese Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Yang CaoFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a major contributor to global cancer-related mortality. Serglycin (SRGN) is involved in the progression of various cancers, and its overexpression is related to poor prognosis in HCC patients. Its biological role in HCC aggressiveness is unknown. This study aims to elucidate the mechanism of SRGN in HCC. Via

Indexed as

Adaptor Proteins, Signal TransducingCarcinoma, HepatocellularCell Adhesion MoleculesLiver NeoplasmsVesicular Transport ProteinsAnimalsCell Line, TumorCell MovementGene Expression Regulation, NeoplasticHumansMaleMiceMice, Inbred BALB CMice, NudeSignal TransductionTranscription FactorsAdaptor Proteins, Signal TransducingCell Adhesion MoleculesTranscription FactorsVesicular Transport ProteinsYAP1 protein, humanYAP-Signaling ProteinsCRISPLD2Hepatocellular carcinomaSRGNTranscriptomeTumor progression

Identifiers

PMID40384866
PMCPMC12080381

What OpenQuestion holds

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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.