Evidence map›Paper›PMID 32918700›Full record

ArticleHuman cell2020

LncRNA ADAMTS9-AS1, as prognostic marker, promotes cell proliferation and EMT in colorectal cancer.

Wanjing Chen, Qian Tu, Liang Yu, Yanyan Xu, Gang Yu, Benli Jia, Yunsheng Cheng, Yong Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
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

21 citing papers in PubMed, 41 citations in OpenAlex.

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  9. Potentials of long non-coding RNAs as biomarkers of colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
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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.

Wanjing ChenDepartment of General Surgery, Economic and Technological Development District, The Second Hospital of Anhui Medical University, No.678 Furong Road, Hefei, Anhui, China.
Qian Tu *Department of General Surgery, Economic and Technological Development District, The Second Hospital of Anhui Medical University, No.678 Furong Road, Hefei, Anhui, China.
Liang YuDepartment of General Surgery, Economic and Technological Development District, The Second Hospital of Anhui Medical University, No.678 Furong Road, Hefei, Anhui, China.
Yanyan XuDepartment of General Surgery, Economic and Technological Development District, The Second Hospital of Anhui Medical University, No.678 Furong Road, Hefei, Anhui, China.
Gang YuDepartment of General Surgery, Economic and Technological Development District, The Second Hospital of Anhui Medical University, No.678 Furong Road, Hefei, Anhui, China.
Benli JiaDepartment of General Surgery, Economic and Technological Development District, The Second Hospital of Anhui Medical University, No.678 Furong Road, Hefei, Anhui, China.
Yunsheng ChengDepartment of General Surgery, Economic and Technological Development District, The Second Hospital of Anhui Medical University, No.678 Furong Road, Hefei, Anhui, China. cheng_yunailg89@yeah.net.
Yong WangDepartment of General Surgery, Economic and Technological Development District, The Second Hospital of Anhui Medical University, No.678 Furong Road, Hefei, Anhui, China. Drwangyong123@126.com.ORCID http://orcid.org/0000-0002-0523-299X
Anhui Medical University · CN

Funding

2019 Provincial Key Laboratory of Medical Physics and Technology Safety and Security Open Fund LMPT201908
6 · The paper itself

Abstract

The long non-coding RNA antisense 1 ADAMTS9-AS1 has been reported to predict the survival in several tumors, including bladder cancer and breast cancer. However, the clinical significance and biological behaviors of ADAMTS9-AS1 in colorectal cancer (CRC) have not been reported yet. In this study, the expression of ADAMTS9-AS1 was measured in CRC tissues and cell lines using quantitative real-time PCR analysis. The clinical significance of ADAMTS9-AS1 was evaluated with Chi-squared test, Kaplan-Meier method and Cox regression analysis in CRC patients. CCK8 assay, colony formation assay, flow cytometry and transwell assay were used to explore the biological function of ADAMTS9-AS1 knockdown in CRC cell lines (SW1116 and HT29). We further explore the role of ADAMTS9-AS1 in vivo though xenograft tumor assay. Our data showed that ADAMTS9-AS1 expression level was significantly up-regulated in CRC tissues and cell lines compared with corresponding controls. High ADAMTS9-AS1 level was associated with TNM stage, lymph node invasion and worse survival prognosis. Depletion of ADAMTS9-AS1 significantly suppressed cell proliferation, G1/S transition, migration and invasion, as well as suppressed CDK4/Cyclin D1 and epithelial-mesenchymal transition (EMT). To sum up, these findings illustrated that ADAMTS9-AS1 might be a promising therapeutic target and prognostic factor for CRC.

Indexed as

Gene ExpressionADAMTS9 ProteinCell Line, TumorCell ProliferationColorectal NeoplasmsEpithelial-Mesenchymal TransitionG1 PhaseHumansLymphatic MetastasisMolecular Targeted TherapyNeoplasm InvasivenessNeoplasm StagingPrognosisS PhaseUp-RegulationADAMTS9 ProteinADAMTS9 protein, humanADAMTS9-AS1CRCEMTG1/S transitionPrognosisProliferation

Identifiers

PMID32918700
OpenAlexW3086751010

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.