Evidence map›Paper›PMID 27468213›Full record

ArticleWorld journal of gastroenterology2016

Glucose deprivation induces chemoresistance in colorectal cancer cells by increasing ATF4 expression.

Ya-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Yu-Gang Wang, Zhao-Hui Huang

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

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  12. Lobaplatin promotesCell death & disease · 2019
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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 1 institution in 1 country.

Ya-Ling HuYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
Yuan YinYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
He-Yong LiuYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
Yu-Yang FengYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
Ze-Hua BianYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
Le-Yuan ZhouYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
Ji-Wei ZhangYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
Bo-Jian FeiYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
Yu-Gang WangYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
Zhao-Hui HuangYa-Ling Hu, Yuan Yin, He-Yong Liu, Yu-Yang Feng, Ze-Hua Bian, Le-Yuan Zhou, Ji-Wei Zhang, Bo-Jian Fei, Zhao-Hui Huang, Wuxi Oncology Institute, Affiliated Hospital of Jiangnan University, Wuxi 214062, Jiangsu Province, China.
CAE (Canada) · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the role of activating transcription factor 4 (ATF4) in glucose deprivation (GD) induced colorectal cancer (CRC) drug resistance and the mechanism involved.

methodsChemosensitivity and apoptosis were measured under the GD condition. Inhibition of ATF4 using short hairpin RNA in CRC cells under the GD condition and in ATF4-overexpressing CRC cells was performed to identify the role of ATF4 in the GD induced chemoresistance. Quantitative real-time RT-PCR and Western blot were used to detect the mRNA and protein expression of drug resistance gene 1 (MDR1), respectively.

resultsGD protected CRC cells from drug-induced apoptosis (oxaliplatin and 5-fluorouracil) and induced the expression of ATF4, a key gene of the unfolded protein response. Depletion of ATF4 in CRC cells under the GD condition can induce apoptosis and drug re-sensitization. Similarly, inhibition of ATF4 in the ATF4-overexpressing CRC cells reintroduced therapeutic sensitivity and apoptosis. In addition, increased MDR1 expression was observed in GD-treated CRC cells.

conclusionThese data indicate that GD promotes chemoresistance in CRC cells through up-regulating ATF4 expression.

Indexed as

Tumor MicroenvironmentActivating Transcription Factor 4Antineoplastic Combined Chemotherapy ProtocolsApoptosisATP Binding Cassette Transporter, Subfamily B, Member 1Blotting, WesternCell Line, TumorCell ProliferationColorectal NeoplasmsDrug Resistance, NeoplasmeIF-2 KinaseEndoplasmic Reticulum Chaperone BiPFluorouracilGene Knockdown TechniquesGlucoseHCT116 CellsActivating Transcription Factor 4ATF4 protein, humanATP Binding Cassette Transporter, Subfamily B, Member 1EIF2AK3 protein, humaneIF-2 KinaseEndoplasmic Reticulum Chaperone BiPFluorouracilGlucoseHeat-Shock ProteinsOrganoplatinum CompoundsOxaliplatin5-FluorouracilATF4ChemoresistanceGlucose deprivationOxaliplatin

Identifiers

PMID27468213
PMCPMC4945982
OpenAlexW2502406249

What OpenQuestion holds

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Registered trials

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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.