Evidence map›Paper›PMID 28751279›Full record

ArticleCellular signalling2017

The extracellular role of DNA damage repair protein APE1 in regulation of IL-6 expression.

Somsubhra Nath, Shrabasti Roychoudhury, Matthew J Kling, Heyu Song, Pranjal Biswas, Ashima Shukla, Hamid Band, Shantaram Joshi, Kishor K Bhakat

Abstract read
In one paragraph

Article in Cellular signalling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

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  14. 17Biomedicines · 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

9 authors at 1 institution in 1 country.

Somsubhra NathDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Shrabasti RoychoudhuryDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Matthew J KlingDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Heyu SongDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Pranjal BiswasDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Ashima ShuklaDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Hamid BandDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA; Eppley Institute for Cancer Research, University of Nebraska Medical Center, Omaha, NE, USA; Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, USA.
Shantaram JoshiDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Kishor K BhakatDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA; Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, USA. Electronic address: kishor.bhakat@unmc.edu.
University of Nebraska Medical Center · US

Funding

Regulatory Functions of APE1 acetylationR01CA148941 · NCI · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BHAKAT, KISHOR K · 2011 to 2015
$1.4M
Cancer Therapeutic Resistance: Implication of AcAPE1 Mediated DNA Repair and T-Cell Based ImmunotherapyF99CA223064 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ROYCHOUDHURY, SHRABASTI · 2017 to 2018
$61k
NCI NIH HHS F99 CA223064NCI NIH HHS R01 CA148941
6 · The paper itself

Abstract

The human apurinic/apyrimidinic endonuclease 1 (APE1) is a pleiotropic nuclear protein with roles in DNA base excision repair pathway as well as in regulation of transcription. Recently, the presence of extracellular plasma APE1 was reported in endotoxemic rats. However, the biological significance and the extracellular function of APE1 remain unclear. In this study, we found that monocytes secrete APE1 upon inflammatory challenges. Challenging the monocytic cells with extracellular APE1 resulted in the increased expression and secretion of the pro-inflammatory cytokine IL-6. Additionally, the extracellular APE1 treatment activated the transcription factor NF-κB, followed by its increased occupancy at the IL-6 promoter, resulting in the induction of IL-6 expression. APE1-induced IL-6 further served to elicit autocrine and paracrine cellular responses. Moreover, the extracellular IL-6 promoted the secretion of APE1, thus indicating a functional feedforward loop in this pathway. Furthermore, we show that APE1 is secreted through extracellular vesicles formation via endosomal sorting complex required for transport (ESCRT)-dependent pathway. Together, our study demonstrates a novel role of extracellular APE1 in IL-6-dependent cellular responses.

Indexed as

Gene Expression RegulationAniline CompoundsAnimalsAutocrine CommunicationBenzylidene CompoundsDNA-(Apurinic or Apyrimidinic Site) LyaseDNA RepairEndosomal Sorting Complexes Required for TransportExtracellular VesiclesHCT116 CellsHumansInterleukin-6MiceMonocytesNF-kappa BParacrine CommunicationAniline CompoundsAPEX1 protein, humanBenzylidene CompoundsDNA-(Apurinic or Apyrimidinic Site) LyaseEndosomal Sorting Complexes Required for TransportGW 4869Interleukin-6NF-kappa BApurinic/apyrimidinic endonuclease 1 (APE1)Interleukin 6 (IL-6)Lipopolysaccharide (LPS)NF-kappa B (NF-κB)Secretion

Identifiers

PMID28751279
PMCPMC5592147
OpenAlexW2739031520

What OpenQuestion holds

Textmetadata
LicenceTDM
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.