Evidence map›Paper›PMID 30899394›Full record

ArticleAmerican journal of translational research2019

Long noncoding RNA HCP5 contributes to epithelial-mesenchymal transition in colorectal cancer through ZEB1 activation and interacting with miR-139-5p.

Cheng Yang, Junjun Sun, Weifeng Liu, Yanhui Yang, Zhijie Chu, Tianbao Yang, Yang Gui, Du Wang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

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  10. Silencing of Long Noncoding RNA HLA Complex P5 (BioMed research international · 2022
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  14. Down-regulation of HCP5 inhibits cell proliferation, migration, and invasion through regulating EPHA7 by competitively binding miR-101 in osteosarcoma.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
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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 1 institution in 1 country.

Cheng YangDepartment of Hepatobiliary, Henan University of Science and Technology First Affiliated Hospital Luoyang 471000, Henan Province, China.
Junjun SunDepartment of Hepatobiliary, Henan University of Science and Technology First Affiliated Hospital Luoyang 471000, Henan Province, China.
Weifeng LiuDepartment of Hepatobiliary, Henan University of Science and Technology First Affiliated Hospital Luoyang 471000, Henan Province, China.
Yanhui YangDepartment of Hepatobiliary, Henan University of Science and Technology First Affiliated Hospital Luoyang 471000, Henan Province, China.
Zhijie ChuDepartment of Hepatobiliary, Henan University of Science and Technology First Affiliated Hospital Luoyang 471000, Henan Province, China.
Tianbao YangDepartment of Hepatobiliary, Henan University of Science and Technology First Affiliated Hospital Luoyang 471000, Henan Province, China.
Yang GuiDepartment of Hepatobiliary, Henan University of Science and Technology First Affiliated Hospital Luoyang 471000, Henan Province, China.
Du WangDepartment of Hepatobiliary, Henan University of Science and Technology First Affiliated Hospital Luoyang 471000, Henan Province, China.
First Affiliated Hospital of Henan University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) play key roles in various malignancy pathogenesis. However, the mechanisms remain poorly understood in the development and progression of colorectal cancer (CRC). Here, we focused on the specific role of human leukocyte antigen (HLA) Complex P5 (HCP5) in CRC. Quantitative real-time PCR (qRT-PCR) analysis and western blot were used to assess the expression of HCP5 in CRC tissues. The association between the expressions of HCP5 and miR-139-5p was assessed by Pearson's correlation analysis. The prognosis of CRC patients was analyzed by Kaplan-Meier survival analysis. Specific siRNAs were stably transfected into CRC cells with lentivirus approaches. The proliferative, migrative and invasive capacities of CRC cells were detected by Transwell, MTT and scratch assay, respectively. Dual-luciferase assay was performed to measure miR-139-5p-targeted relationship with lncRNA HCP5. HCP5 overexpression and of miR-139-5p downregulation were dramatically correlated with low TNM stage, poor differentiation, low tumor depth invasion in CRC patients (P < 0.05). Besides, HCP5 overexpression or ZEB1 knockdown repressed Snail family transcriptional repressor (SNAI) and vimentin expressions, upregulated E-cadherin expression, and inhibited cell proliferation and metastasis (P < 0.05). Moreover, luciferase reporter assay demonstrated that miR-139-5p was a directly target of HCP5 (P < 0.05). Overall, the present study indicated that HCP5 played a key regulator in CRC development and progression by targeting HCP5/miR-139-5p/ZEB1 axis, which may serve as a novel therapeutic target for CRC therapy.

Indexed as

Colorectal cancer (CRC)human leukocyte antigen (HLA) complex P5 (HCP5)long noncoding RNAs (lncRNA)metastasismiR-139-5pproliferation

Identifiers

PMID30899394
PMCPMC6413275
OpenAlexW2999836864

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.