Evidence map›Paper›PMID 30306507›Full record

ArticleMolecular biology reports2018

β2-AR regulates the expression of AKR1B1 in human pancreatic cancer cells and promotes their proliferation via the ERK1/2 pathway.

Ming-Bing Xiao, Dan-Dan Jin, Yu-Jie Jiao, Wen-Kai Ni, Jin-Xia Liu, Li-Shuai Qu, Cui-Hua Lu, Run-Zhou Ni, Feng Jiang, Wei-Chang Chen

Abstract read
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In one paragraph

Article in Molecular biology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  6. Review
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  13. The Role of the FOXO1/βInternational journal of molecular sciences · 2021
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  14. An Advanced Systems Pharmacology Strategy RevealsFrontiers in cell and developmental biology · 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

10 authors at 2 institutions in 1 country.

Ming-Bing XiaoDepartment of Gastroenterology, The First Affiliated Hospital of Soochow University, No. 188, Shizi Road, Suzhou, 215006, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0003-3372-1069
Dan-Dan JinDepartment of Gastroenterology, Affiliated Hospital of Nantong University, No. 20, Xisi Road, Nantong, 226001, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0002-9493-2508
Yu-Jie JiaoDepartment of Gastroenterology, Affiliated Hospital of Nantong University, No. 20, Xisi Road, Nantong, 226001, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0003-2781-957X
Wen-Kai NiDepartment of Gastroenterology, Affiliated Hospital of Nantong University, No. 20, Xisi Road, Nantong, 226001, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0001-6056-1924
Jin-Xia LiuDepartment of Gastroenterology, Affiliated Hospital of Nantong University, No. 20, Xisi Road, Nantong, 226001, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0001-8327-2228
Li-Shuai QuDepartment of Gastroenterology, Affiliated Hospital of Nantong University, No. 20, Xisi Road, Nantong, 226001, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0001-8562-678X
Cui-Hua LuDepartment of Gastroenterology, Affiliated Hospital of Nantong University, No. 20, Xisi Road, Nantong, 226001, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0002-1377-5820
Run-Zhou NiDepartment of Gastroenterology, Affiliated Hospital of Nantong University, No. 20, Xisi Road, Nantong, 226001, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0001-8187-185X
Feng JiangDepartment of Gastroenterology, Affiliated Hospital of Nantong University, No. 20, Xisi Road, Nantong, 226001, Jiangsu, People's Republic of China. jf6665@126.com.ORCID http://orcid.org/0000-0001-5416-4316
Wei-Chang ChenDepartment of Gastroenterology, The First Affiliated Hospital of Soochow University, No. 188, Shizi Road, Suzhou, 215006, Jiangsu, People's Republic of China. weichangchensz@163.com.ORCID http://orcid.org/0000-0001-8849-6204
Nantong University · CNSoochow University · CN

Funding

National Natural Science Foundation of China 81472272National Natural Science Foundation of China 81602114Natural Science Foundation of Jiangsu Province BK20161286Postdoctoral Science Foundation of China 2017M620221Social Development Foundation of Nantong City MS12017002-6Social Development Foundation of Nantong City MS22016056
6 · The paper itself

Abstract

Psychological stress has been recognized as a well-documented risk factor associated with β2-adrenergic receptor (β2-AR) in the development of pancreatic cancer. Aldo-keto reductase 1 member B1 (AKR1B1) is a potential interacting partner of β2-AR, but the effect of their interaction on pancreatic cancer cells is not known at present. We found a positive correlation between AKR1B1 and β2-AR expression in pancreatic cancer tissue samples, and co-localization of these proteins in the human pancreatic cancer BXPC-3 cell line. Compared to the controls, the CFPAC-1 and PANC-1 pancreatic cancer cells overexpressing β2-AR and AKR1B1 respectively showed significantly higher proliferation rates, which is attributed to higher proportion of cells in the S phase and decreased percentage of early apoptotic cells. Furthermore, overexpression of β2-AR led to a significant increase in the expression of AKR1B1 and phosphorylated extracellular signal-regulated kinase (p-ERK1/2). Overexpression of AKR1B1 significantly decreased β2-AR levels and increased that of p-ERK1/2. Taken together, β2-AR directly interacted with and up-regulated AKR1B1 in pancreatic cancer cells, and promoted their proliferation and inhibited apoptosis via the ERK1/2 pathway. Our findings also highlight the β2-AR-AKR1B1 axis as a potential therapeutic target for pancreatic cancer.

Indexed as

AdultAgedAged, 80 and overAldehyde ReductaseAldo-Keto ReductasesApoptosisCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMaleMAP Kinase Signaling SystemMiddle AgedMitogen-Activated Protein Kinase 3PancreasAKR1B1 protein, humanAldehyde ReductaseAldo-Keto ReductasesMitogen-Activated Protein Kinase 3Proto-Oncogene Proteins c-aktReceptors, Adrenergic, beta-2AKR1B1ERK1/2Pancreatic cancerProliferationβ2-AR

Identifiers

PMID30306507
OpenAlexW2897267594

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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.