Evidence map›Paper›PMID 30063110›Full record

ArticleMolecular oncology2018

ER stress-related ATF6 upregulates CIP2A and contributes to poor prognosis of colon cancer.

Chun-Yu Liu, Chia-Chi Hsu, Tzu-Ting Huang, Chia-Han Lee, Ji-Lin Chen, Shung-Haur Yang, Jeng-Kai Jiang, Wei-Shone Chen, Kuan-Der Lee, Hao-Wei Teng

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 77 citations in OpenAlex.

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  19. Endoplasmic Reticulum Stress in Renal Cell Carcinoma.International journal of molecular sciences · 2023
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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 4 institutions in 1 country.

Chun-Yu LiuDivision of Medical Oncology, Department of Oncology, Center for Immuno-Oncology, Taipei Veterans General Hospital, Taiwan.
Chia-Chi HsuDivision of Medical Oncology, Department of Oncology, Center for Immuno-Oncology, Taipei Veterans General Hospital, Taiwan.
Tzu-Ting HuangDivision of Medical Oncology, Department of Oncology, Center for Immuno-Oncology, Taipei Veterans General Hospital, Taiwan.
Chia-Han LeeDivision of Medical Oncology, Department of Oncology, Center for Immuno-Oncology, Taipei Veterans General Hospital, Taiwan.
Ji-Lin ChenDivision of Medical Oncology, Department of Oncology, Center for Immuno-Oncology, Taipei Veterans General Hospital, Taiwan.
Shung-Haur YangSchool of Medicine, National Yang-Ming University, Taipei, Taiwan.
Jeng-Kai JiangSchool of Medicine, National Yang-Ming University, Taipei, Taiwan.
Wei-Shone ChenSchool of Medicine, National Yang-Ming University, Taipei, Taiwan.
Kuan-Der LeeDivision of Hematology and Oncology, Department of Internal Medicine, Taipei Medical University Hospital, Taiwan.
Hao-Wei TengDivision of Medical Oncology, Department of Oncology, Center for Immuno-Oncology, Taipei Veterans General Hospital, Taiwan.
Taipei Veterans General Hospital · TWNational Yang Ming Chiao Tung University · TWNational Taipei University · TWTaipei Medical University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endoplasmic reticulum (ER) stress is an adaptive response to various stress conditions and plays emerging roles in cancer. Activating transcription factor 6 (ATF6), one of the three major ER stress transducers, has been shown to contribute to chemoresistance by altering cancer cell survival. Cancerous inhibitor of protein phosphatase 2A (CIP2A) is an oncogene, and its expression has been correlated with the prognosis of patients with cancer. In this study, we aimed to explore the relationship between ER stress-related ATF signaling and CIP2A. We found that CIP2A expression was positively correlated with ATF6 expression by analyzing publicly available RNA sequence data of patients with colorectal cancer (The Cancer Genome Atlas, TCGA). In addition, we demonstrated that tunicamycin-induced ER stress in vitro upregulated ATF6 and CIP2A. Mechanistically, we found that ATF6 directly bound to the CIP2A promoter and induced CIP2A gene expression, which contributed to colon cancer cell survival. Furthermore, knockdown of CIP2A reduced the viability of cells under ER stress. Most importantly, immunohistochemical analysis of a tissue microarray from a colon cancer patient cohort showed that higher expression levels of ATF6 and CIP2A were associated with a trend toward poor prognosis. Taken together, our results show that ER stress-related ATF6 upregulates CIP2A and contributes to the prognosis of colon cancer. Targeting CIP2A may disrupt ER stress-mediated colon cancer cell survival and thus improve the prognosis of patients with colon cancer.

Indexed as

Endoplasmic Reticulum StressUp-RegulationActivating Transcription Factor 6AgedAutoantigensCell Line, TumorColonic NeoplasmsFemaleHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsMaleMembrane ProteinsMiddle AgedMultivariate AnalysisPrognosisActivating Transcription Factor 6AutoantigensCIP2A protein, humanIntracellular Signaling Peptides and ProteinsMembrane ProteinsATF6CIP2Acolon cancerER stress

Identifiers

PMID30063110
PMCPMC6166000
OpenAlexW2885558936

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.