Evidence map›Paper›PMID 35798928›Full record

ArticleCurrent medical science2022

Arginine ADP-ribosyltransferase 1 Regulates Glycolysis in Colorectal Cancer via the PI3K/AKT/HIF1α Pathway.

Wen-Bo Long, Xia Pu, Yi Tang, Ming Li, Yun Liu, Qin She, Ya-Lan Wang, Qin-Xi Guo

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Article in Current medical science, 2022. 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
1.9field-weighted citation impact, top 13% 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, 20 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

8 authors at 2 institutions in 1 country.

Wen-Bo Long *Department of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, 646099, China.
Xia Pu *Clinical Skills Center of Affiliated Hospital of Southwest Medical University, Luzhou, 646099, China.
Yi TangDepartment of Pathology, School of Basic Medicine, Chongqing Medical University, Chongqing, 400016, China.
Ming LiDepartment of Pathology, School of Basic Medicine, Chongqing Medical University, Chongqing, 400016, China.
Yun LiuDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, 646099, China.
Qin SheDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, 646099, China.
Ya-Lan WangDepartment of Pathology, School of Basic Medicine, Chongqing Medical University, Chongqing, 400016, China. wangyalan074@126.com.
Qin-Xi GuoDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, 646099, China. gqx_77@163.com.
Affiliated Hospital of Southwest Medical University · CNChongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveArginine ADP-ribosyltransferase 1 (ART1) is involved in the regulation of a diverse array of pathophysiological processes, including proliferation, invasion, apoptosis, autophagy and angiogenesis of colorectal cancer (CRC) cells. However, how ART1 regulates glycolysis in CRC remains elusive.

methodsTo elucidate the role of ART1 in glycolysis in CRC, we assessed the protein level of ART1, hypoxia-inducible factor 1α (HIF1α), and glucose transporter type 1 (GLUT1) in 61 CRC tumor tissue specimens obtained from patients with different 2-[

resultsThe expression of ART1 and GLUT1 was significantly associated with FDG uptake (P=0.037 and P=0.022, respectively) in CRC tissues. Furthermore, the expression of hexokinase 2 (HK2) and lactate dehydrogenase (LDH) was upregulated in ART1-overexpressed CT26 cells, but was downregulated in ART1-knockdown CT26 cells. The volume and weight of subcutaneously transplanted tumors were markedly increased in the ART1-overexpressed BALB/c mice group and decreased in the ART1-knockdown group. In CT26 cells, the overexpression of ART1 promoted the expression levels of HK2 and LDH, and knockdown of ART1 suppressed them in the CT26 tumors. In both normal and hypoxic conditions, ART1 expression was associated with the protein level of phospho-serine/threonine kinase (p-AKT), HIF1α, and GLUT1 but not with that of AKT in CT26 cells and subcutaneous transplanted tumors.

conclusionART1 plays a crucial role in the elevation of glucose consumption in CT26 cells and may regulate GLUT1-dependent glycolysis in CRC via the PI3K/AKT/HIF1α pathway.

Indexed as

AdenocarcinomaColonic NeoplasmsADP Ribose TransferasesAnimalsArginineCell Line, TumorFluorodeoxyglucose F18Glucose Transporter Type 1GlycolysisHypoxia-Inducible Factor 1, alpha SubunitMicePhosphatidylinositol 3-KinasesPositron Emission Tomography Computed TomographyProto-Oncogene Proteins c-aktADP Ribose TransferasesArginineFluorodeoxyglucose F18Glucose Transporter Type 1Hif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktarginine ADP-ribosyltransferases 1colorectal cancerglucose transporter type 1hypoxia-inducible factorWarburg effect

Identifiers

PMID35798928
OpenAlexW4284899624

What OpenQuestion holds

Textmetadata
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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.