Evidence map›Paper›PMID 34488772›Full record

ArticleCancer cell international2021

Carcinogenic effect of adenylosuccinate lyase (ADSL) in prostate cancer development and progression through the cell cycle pathway.

Jinling Liao, Qiong Song, Jie Li, Kechen Du, Yang Chen, Chunlin Zou, Zengnan Mo

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

10 citing papers in PubMed, 12 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

7 authors at 2 institutions in 2 countries.

Jinling Liao *Center for Genomic and Personalized Medicine, Guangxi key Laboratory for Genomic and Personalized Medicine, Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Guangxi Medical University, No. 22 Shuangyong Road, Guangxi Zhuang Autonomous Region, Nanning, 530021, China.
Qiong Song *Key Laboratory of Longevity and Aging-Related Disease of Chinese Ministry of Education, Center for Translational Medicine, School of Preclinical Medicine, Guangxi Medical University, No. 22 Shuangyong Road, Guangxi Zhuang Autonomous Region, Nanning, 530021, China.
Jie Li *The Reproductive Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, 530218, China.
Kechen DuKey Laboratory of Longevity and Aging-Related Disease of Chinese Ministry of Education, Center for Translational Medicine, School of Preclinical Medicine, Guangxi Medical University, No. 22 Shuangyong Road, Guangxi Zhuang Autonomous Region, Nanning, 530021, China.
Yang ChenCenter for Genomic and Personalized Medicine, Guangxi key Laboratory for Genomic and Personalized Medicine, Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Guangxi Medical University, No. 22 Shuangyong Road, Guangxi Zhuang Autonomous Region, Nanning, 530021, China. chenyang@gxmu.edu.cn.ORCID http://orcid.org/0000-0002-1282-0204
Chunlin ZouKey Laboratory of Longevity and Aging-Related Disease of Chinese Ministry of Education, Center for Translational Medicine, School of Preclinical Medicine, Guangxi Medical University, No. 22 Shuangyong Road, Guangxi Zhuang Autonomous Region, Nanning, 530021, China. zouchunlin@gxmu.edu.cn.
Zengnan MoCenter for Genomic and Personalized Medicine, Guangxi key Laboratory for Genomic and Personalized Medicine, Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Guangxi Medical University, No. 22 Shuangyong Road, Guangxi Zhuang Autonomous Region, Nanning, 530021, China. zengnanmo@hotmail.com.
Guangxi Medical University · CNThe People's Hospital of Guangxi Zhuang Autonomous Region · CN

Funding

National Natural Science Foundation of China 81670750National Natural Science Foundation of China 81901538National Natural Science Foundation of China 82060145
6 · The paper itself

Abstract

backgroundProstate cancer (PCa) is still a serious male malignant disease across the world. However, no exact pathogenesis had been explained. Although adenylosuccinate lyase (ADSL) gene was identified to be important in PCa early in 1987, its comprehensive functions for PCa have not been presented.

methodsThe cBioPortal for Cancer Genomics, Oncomine and GEO database were retrieved to investigate the associations between of the ADSL gene and PCa. Then, the PC-3, DU145 and C4-2B cell lines were applied in vitro experiments. RNA sequencing and further western blot (WB) were applied to explore the potential mechanisms of ADSL gene in PCa.

resultsBased on PCa clinical datasets, we firstly found ADSL gene highly expressed in PCa tissues. Moreover, its transcript level increased in the metastatic PCa further. Elevated ADSL gene expression indicated a poor prognosis of PCa. While inhibiting the expression of ADSL with siRNA, the ability of cell proliferation and migration all declined markedly, with increased cell apoptosis inversely. Most of cells were blocked in the G0/G1 phase. Additionally, RNA sequencing also discovered the inactivity of cell cycle pathway after ADSL knockdown, which had also confirmed on the proteins levels.

conclusionsOur study identified the ADSL as an oncogene of PCa through regulating the cell cycle pathway firstly, with explicit cell and clinical phenotypes. Further mechanisms were needed to confirm its carcinogenic effect.

Indexed as

ADSLCell cycleOncogeneProstate cancerVitro experiment

Identifiers

PMID34488772
PMCPMC8419980
OpenAlexW3196788824

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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.