Evidence map›Paper›PMID 40760131›Full record

ArticleScientific reports2025

PGRP-S promotes hepatocellular carcinoma progression via MAPK/ERK pathway by interaction with TTC1.

Huifang Zhu, Shuang Feng, Sizhen Lv, Di Zhao, Xuanhe Chang, Shangqian Fan, Xia Wang, Xinlai Qian

RetractedAbstract readRetracted Publication
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Huifang ZhuDepartment of Pathology, The Third Affiliated Hospital of Xinxiang Medical University, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China. zhf8382@163.com.
Shuang FengDepartment of Pathology, The Third Affiliated Hospital of Xinxiang Medical University, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.
Sizhen LvDepartment of Pathology, The Third Affiliated Hospital of Xinxiang Medical University, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.
Di ZhaoDepartment of Pathology, The Third Affiliated Hospital of Xinxiang Medical University, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.
Xuanhe ChangThe First Bethune Clinical Medical College of Ji Lin University, Changchun, Jilin, China.
Shangqian FanDepartment of Pathology, The Third Affiliated Hospital of Xinxiang Medical University, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.
Xia WangDepartment of Pathology, The Third Affiliated Hospital of Xinxiang Medical University, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.
Xinlai QianDepartment of Pathology, The Third Affiliated Hospital of Xinxiang Medical University, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China. qxlfssws@163.com.

Funding

Medical Science and Technology Research Program of Henan Province SBGJ 202002096Science and Technology Development Project of Henan Province 222102310145
6 · The paper itself

Abstract

Abnormal expression of PGRP-S plays an important role in the development and progression of hepatocellular carcinoma (HCC), although the mechanism has remained elusive. In this study, we aimed to investigate the biological function and potential mechanism of PGRP-S in HCC. We found that PGRP-S was upregulated in HCC tissues compared to adjacent tissues. The increased expression of PGRP-S correlated with the differentiation and lymph node metastasis of HCC. PGRP-S obviously promoted HCC cell proliferation, migration and invasion in vitro. In vivo nude mouse models showed that PGRP-S enhanced tumor growth and pulmonary metastasis. Mechanistically, PGRP-S interacted with TTC1 and activated MAPK/ERK pathway, leading to HCC cell proliferation, migration and invasion. Therfore, our conclusion is PGRP-S promotes HCC cell proliferation, migration and invasion by activating MAPK/ERK pathway, which provides a new potential strategy for HCC treatment by targeting PGRP-S-TTC1 axis.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMAP Kinase Signaling SystemAnimalsCell Line, TumorCell MovementCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMaleMiceMice, Inbred BALB CMice, NudeMiddle AgedHepatocellular carcinomaMigrationPGRP-SProliferationTTC1

Identifiers

PMID40760131
PMCPMC12322062

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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.