Evidence map›Paper›PMID 32888357›Full record

ArticleCancer science2021

Ribosome assembly factor URB1 contributes to colorectal cancer proliferation through transcriptional activation of ATF4.

Tao Wang, Lai-Yuan Li, Yi-Feng Chen, Si-Wu Fu, Zhi-Wei Wu, Bin-Bin Du, Xiong-Fei Yang, Wei-Sheng Zhang, Xiang-Yong Hao, Tian-Kang Guo

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 18 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

10 authors at 3 institutions in 1 country.

Tao WangDepartment of Colorectal Surgery, Gansu Provincial People's Hospital, Lanzhou, China.
Lai-Yuan LiDepartment of Colorectal Surgery, Gansu Provincial People's Hospital, Lanzhou, China.
Yi-Feng ChenDepartment of Colorectal Surgery, Gansu Provincial People's Hospital, Lanzhou, China.
Si-Wu FuThe School of Medical College, Northwest Minzu University, Lanzhou, China.
Zhi-Wei WuThe School of Preclinical Medicine, Gansu University of Traditional Chinese Medicine, Lanzhou, China.
Bin-Bin DuDepartment of Colorectal Surgery, Gansu Provincial People's Hospital, Lanzhou, China.
Xiong-Fei YangDepartment of Colorectal Surgery, Gansu Provincial People's Hospital, Lanzhou, China.
Wei-Sheng ZhangDepartment of Colorectal Surgery, Gansu Provincial People's Hospital, Lanzhou, China.
Xiang-Yong HaoDepartment of General Surgery, Gansu Provincial People's Hospital, Lanzhou, China.
Tian-Kang GuoThe First School of Clinical Medicine, Lanzhou University, Lanzhou, China.ORCID https://orcid.org/0000-0002-1295-2557
Gansu Provincial Hospital · CNGansu University of Traditional Chinese Medicine · CNMinzu University of China · CN

Funding

Nature Science Foundation for Young Scientists and Technology Planning Project 18JR3RA058The Health Industry Scientific Research Project of Gansu Province GSWSKY-2019-69The National Natural Science Foundation of China 81660157The Nature Science Foundation for Young Scientists & Technology Planning Project of Gansu Province 18JR3RA058The Research Projects of Gansu Provincial People's Hospital 18GSSY3-1The Research Projects of Gansu Provincial People's Hospital 18GSSY4-2The Research Projects of Gansu Provincial People's Hospital 19SYPYB-6The Research Projects of Gansu Provincial People's Hospital 19SYPYB-7
6 · The paper itself

Abstract

Ribosome assembly factor URB1 is essential for ribosome biogenesis. However, its latent role in cancer remains unclear. Analysis of The Cancer Genome Atlas database and clinical tissue microarray staining showed that URB1 expression was upregulated in colorectal cancer (CRC) and prominently related to clinicopathological characteristics. Silencing of URB1 hampered human CRC cell proliferation and growth in vitro and in vivo. Microarray screening, ingenuity pathway analysis, and JASPAR assessment indicated that activating transcription factor 4 (ATF4) and X-box binding protein 1 (XBP1) are potential downstream targets of URB1 and could transcriptionally interact through direct binding. Silencing of URB1 significantly decreased ATF4 and cyclin A2 (CCNA2) expression in vivo and in vitro. Restoration of ATF4 effectively reversed the malignant proliferation phenotype of URB1-silenced CRC cells. Dual-luciferase reporter and ChIP assays indicated that XBP1 transcriptionally activated ATF4 by binding with its promoter region. X-box binding protein 1 colocalized with ATF4 in the nuclei of RKO cells, and ATF4 mRNA expression was positively regulated by XBP1. This study shows that URB1 contributes to oncogenesis and CRC growth through XBP1-mediated transcriptional activation of ATF4. Therefore, URB1 could be a potential therapeutic target for CRC.

Indexed as

Activating Transcription Factor 4Cell Line, TumorCell ProliferationCell Transformation, NeoplasticColorectal NeoplasmsFemaleGene Expression Regulation, NeoplasticHCT116 CellsHumansMaleMiddle AgedNuclear ProteinsRibosomesSignal TransductionTranscriptional ActivationUp-RegulationActivating Transcription Factor 4ATF4 protein, humanNuclear ProteinsURB1 protein, humanX-Box Binding Protein 1ATF4colorectal cancercyclin A2ribosome assembly factorURB1XBP1

Identifiers

PMID32888357
PMCPMC7780016
OpenAlexW3083633875

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.