Evidence map›Paper›PMID 32236884›Full record

ArticleDigestive diseases and sciences2021

PLCD1 Suppressed Cellular Proliferation, Invasion, and Migration via Inhibition of Wnt/β-Catenin Signaling Pathway in Esophageal Squamous Cell Carcinoma.

Xin He, Fan Meng, Zhong-Jian Yu, Xiong-Jie Zhu, Ling-Yu Qin, Xiao-Ran Wu, Zhi-le Liu, Ying Li, Yan-Fang Zheng

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Article in Digestive diseases and sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 21 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

9 authors at 3 institutions in 1 country.

Xin He *The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jangxi Province, China.
Fan Meng *The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jangxi Province, China.
Zhong-Jian YuDepartment of Oncology, Zhujiang Hospital of Southern Medical University, Guangzhou, 510282, China.
Xiong-Jie ZhuDepartment of Oncology, Zhujiang Hospital of Southern Medical University, Guangzhou, 510282, China.
Ling-Yu QinDepartment of Oncology, Zhujiang Hospital of Southern Medical University, Guangzhou, 510282, China.
Xiao-Ran WuDepartment of Oncology, Zhujiang Hospital of Southern Medical University, Guangzhou, 510282, China.
Zhi-le LiuDepartment of Oncology, Zhujiang Hospital of Southern Medical University, Guangzhou, 510282, China.
Ying LiDepartment of Oncology, Zhujiang Hospital of Southern Medical University, Guangzhou, 510282, China.
Yan-Fang ZhengDepartment of Oncology, Zhujiang Hospital of Southern Medical University, Guangzhou, 510282, China. 18665000236@163.com.
Zhujiang Hospital · CNSouthern Medical University · CNFirst Affiliated Hospital of Gannan Medical University · CN

Funding

Jiangxi Provincial Department of Education Project 190842Jiangxi Provincial Department of Education Project 190845the National Natural Science Foundation of China 81960438
6 · The paper itself

Abstract

backgroundPhospholipase C delta 1 (PLCD1) has been found to be abnormally expressed in various cancers. However, the potential roles of PLCD1 in esophageal squamous cell carcinoma (ESCC) are still unknown.

methodsWestern blot and qPCR were used to explore PLCD1 expression in various ESCC cells. MTT, colony formation assays, wound-healing assay, and transwell cell invasion assay were used to examine the cell viability in vitro. Western blot, qPCR, and luciferase assays were used to investigate the effects of PLCD1 on Wnt/β-catenin signaling pathway. The xenograft models in nude mice were established to explore the roles of PLCD1 in vivo.

resultsWe found that the expression of PLCD1 in ESCC cells was significantly downregulated than that in normal esophageal epithelial cells. In addition, upregulation of PLCD1 decreased the capacity of TE-1 and EC18 cells in proliferation, invasion, and migration. Then, the expression of β-catenin/p-β-catenin, C-myc, cyclin D1, MMP9, and MMP7 was investigated. PLCD1 activity was found to be negatively associated with the expression of β-catenin, C-myc, cyclin D1, MMP9, and MMP7. Finally, the activity of PLCD1 in inhibiting ESCC proliferation in vivo was validated.

conclusionThe inhibitory effects of PLCD1 on the proliferation, invasion, and migration of TE-1 and EC18 cells might be associated with inhibition of Wnt/β-catenin signaling pathway. PLCD1 played a key role in inhibiting ESCC carcinogenesis and progression in patients with ESCC.

Indexed as

Animalsbeta CateninCell Line, TumorCell MovementCell ProliferationEsophageal Squamous Cell CarcinomaHumansMiceMice, Inbred BALB CMice, NudeNeoplasm InvasivenessPhospholipase C deltaTumor BurdenWnt Signaling Pathwaybeta CateninPhospholipase C deltaPLCD1 protein, humanEsophageal squamous cell carcinomaPhospholipase C delta 1Wnt/β-catenin signaling pathway

Identifiers

PMID32236884
OpenAlexW3014868241

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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.