Evidence map›Paper›PMID 36602696›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2023

HRCT1, negatively regulated by miR-124-3p, promotes tumor metastasis and the growth of gastric cancer by activating the ERBB2-MAPK pathway.

Feng Hou, Duan-Bo Shi, Xiang-Yu Guo, Rui-Nan Zhao, Hui Zhang, Ran-Ran Ma, Jun-Yi He, Peng Gao

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Feng Hou *Department of Pathology, Qilu Hospital, Shandong University, Wen Hua Xi Road 107, Jinan, 250012, Shandong, People's Republic of China.
Duan-Bo Shi *Department of Pathology, Qilu Hospital, Shandong University, Wen Hua Xi Road 107, Jinan, 250012, Shandong, People's Republic of China.
Xiang-Yu GuoDepartment of Pathology, Qilu Hospital, Shandong University, Wen Hua Xi Road 107, Jinan, 250012, Shandong, People's Republic of China.
Rui-Nan ZhaoDepartment of Pathology, Qilu Hospital, Shandong University, Wen Hua Xi Road 107, Jinan, 250012, Shandong, People's Republic of China.
Hui ZhangDepartment of Pathology, Qilu Hospital, Shandong University, Wen Hua Xi Road 107, Jinan, 250012, Shandong, People's Republic of China.
Ran-Ran MaDepartment of Pathology, Qilu Hospital, Shandong University, Wen Hua Xi Road 107, Jinan, 250012, Shandong, People's Republic of China.
Jun-Yi HeKey Laboratory for Experimental Teratology of the Ministry of Education and Department of Pathology, School of Basic Medicine, Shandong University, Wen Hua Xi Road 44, Jinan, 250012, Shandong, China.
Peng GaoDepartment of Pathology, Qilu Hospital, Shandong University, Wen Hua Xi Road 107, Jinan, 250012, Shandong, People's Republic of China. gaopeng@sdu.edu.cn.ORCID 0000-0002-4721-0887
Shandong University · CNQingdao University · CN

Funding

National Natural Science Foundation of China 81902463National Natural Science Foundation of China 82072665Postdoctoral Research Foundation of China 2020M216897
6 · The paper itself

Abstract

backgroundGastric cancer is the fourth leading cause of cancer-related deaths worldwide. And patient outcomes are poor due to tumor relapse and metastasis. To develop new therapeutic strategies, it is of great importance to explore the mechanism underlying the progression of gastric cancer.

methodsPrimary gastric cancer samples with lymph node metastases (LNM) and without LNM were subjected to mRNA microarray assay. The differentially expressed genes were confirmed by RT-qPCR. HRCT1 protein expression was further detected using an immunohistochemistry (IHC) assay. In vitro and in vivo assays were performed to investigate the role of HRCT1 in tumor invasion, metastasis, and proliferation. The expressions of the downstream target genes of HRCT1 were detected by microarray, RT-qPCR and Western blot assays. Dual-luciferase reporter and Western blot assays were carried out to identify miRNAs target to HRCT1.

resultsHRCT1 was upregulated in gastric cancer, and high expression of HRCT1 was associated with poor overall survival (OS) and disease-free survival (DFS). Moreover, HRCT1protein expression was an independent predictor for poor OS and DFS. HRCT1 could promote gastric cancer cells' migration, invasion, and proliferation in vitro as well as tumor metastasis and growth in vivo. Notably, our data showed that HRCT1 promoted gastric cancer progression by activating the ERBB2-MAPK signaling pathway. At least partially, the expression of HRCT1 could be negatively regulated by miR-124-3p.

conclusionsThe upregulated expression of HRCT1 predicts poor survival for patients with gastric cancer. HRCT1 promotes tumor progression by activating the ERBB2-MAPK pathway. HRCT1, negatively regulated by miR-124-3p, may be a potential therapeutic target for patients with gastric cancer.

Indexed as

MicroRNAsStomach NeoplasmsCell Line, TumorCell MovementCell ProliferationErb-b2 Receptor Tyrosine KinasesGene Expression Regulation, NeoplasticHumansLymphatic MetastasisSignal TransductionERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMicroRNAsMIRN124 microRNA, humanGastric cancerGrowthHRCT1Metastasis

Identifiers

PMID36602696
OpenAlexW4313545735

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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.