Evidence map›Paper›PMID 37184260›Full record

ArticleCancer medicine2023

LPCAT1 enhances the invasion and migration in gastric cancer: Based on computational biology methods and in vitro experiments.

Zu-Xuan Chen, Liang Liang, He-Qing Huang, Jian-Di Li, Rong-Quan He, Zhi-Guang Huang, Rui Song, Gang Chen, Jian-Jun Li, Zheng-Wen Cai and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. 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
0.6field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Association ofBiomedicines · 2025
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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

11 authors at 1 institution in 1 country.

Zu-Xuan ChenDepartment of Medical Oncology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Liang LiangDepartment of General Surgery, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
He-Qing HuangDepartment of Radiotherapy, The First Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.ORCID 0000-0001-6911-3386
Jian-Di LiDepartment of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Rong-Quan HeDepartment of Medical Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Zhi-Guang HuangDepartment of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Rui SongDepartment of Gastroenterology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Gang ChenDepartment of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.ORCID 0000-0003-2402-2987
Jian-Jun LiDepartment of General Surgery, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Zheng-Wen CaiDepartment of Medical Oncology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Jie-An HuangDepartment of Gastroenterology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.ORCID 0000-0003-0431-1888
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimThe biological functions and clinical implications of lysophosphatidylcholine acyltransferase 1 (LPCAT1) remain unclarified in gastric cancer (GC). The aim of the current study was to explore the possible clinicopathological significance of LPCAT1 and its perspective mechanism in GC tissues. MATERIALS AND

methodsThe protein expression and mRNA levels of LPCAT1 were detected from in-house immunohistochemistry and public high-throughput RNA arrays and RNA sequencing. To have a comprehensive understanding of the clinical value of LPCAT1 in GC, all enrolled data were integrated to calculate the expression difference and standard mean difference (SMD). The biological mechanism of LPCAT1 in GC was confirmed by computational biology and in vitro experiments. Migration and invasion assays were also conducted to confirm the effect of LPCAT1 in GC.

resultsBoth protein and mRNA expression levels of LPCAT1 in GC were remarkably higher than those in noncancerous controls. Comprehensively, the SMD of LPCAT1 mRNA was 1.11 (95% CI = 0.86-1.36) in GC, and the summarized AUC was 0.85 based on 15 datasets containing 1727 cases of GC and 940 cases of non-GC controls. Moreover, LPCAT1 could accelerate the invasion and migration of GC by boosting the neutrophil degranulation pathway and disturbing the immune microenvironment.

conclusionAn increased level of LPCAT1 may promote the progression of GC.

Indexed as

Stomach Neoplasms1-Acylglycerophosphocholine O-AcyltransferaseAcyltransferasesCell ProliferationComputational BiologyHumansRNA, MessengerTumor Microenvironment1-Acylglycerophosphocholine O-AcyltransferaseAcyltransferasesRNA, Messengercomputational biologygastric cancerimmunohistochemistryin vitro experimentslysophosphatidylcholine acyltransferase 1 (LPCAT1)standard mean difference (SMD)

Identifiers

PMID37184260
PMCPMC10315734
OpenAlexW4376611562

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.