Evidence map›Paper›PMID 31575655›Full record

ArticleMolecular cancer therapeutics2020

Targeting Histone Chaperone FACT Complex Overcomes 5-Fluorouracil Resistance in Colon Cancer.

Heyu Song, Jiping Zeng, Shrabasti Roychoudhury, Pranjal Biswas, Bhopal Mohapatra, Sutapa Ray, Kayvon Dowlatshahi, Jing Wang, Vimla Band, Geoffrey Talmon and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 17% 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, 23 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

11 authors at 2 institutions in 1 country.

Heyu SongDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska.
Jiping ZengDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska.
Shrabasti RoychoudhuryDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska.
Pranjal BiswasDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska.
Bhopal MohapatraDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska.
Sutapa RayDepartment of Pediatrics, University of Nebraska Medical Center, Omaha, Nebraska.
Kayvon DowlatshahiDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska.
Jing WangEppley Institute for Cancer Research, University of Nebraska Medical Center, Omaha, Nebraska.
Vimla BandDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska.
Geoffrey TalmonDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska.
Kishor K BhakatDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska. kishor.bhakat@unmc.edu.
University of Nebraska Medical Center · USNebraska Medical Center · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Joann B. Sweasy · 1985 to 2026
$55.0M
Regulatory Functions of APE1 acetylationR01CA148941 · NCI · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BHAKAT, KISHOR K · 2011 to 2015
$1.4M
Elucidating the role of acetylation of APE1 in tumor growth and chemoresistanceR03CA235214 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BHAKAT, KISHOR K · 2019 to 2020
$161k
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 P30 CA036727NCI NIH HHS R01 CA148941NCI NIH HHS R03 CA235214
6 · The paper itself

Abstract

Fluorouracil (5-FU) remains a first-line chemotherapeutic agent for colorectal cancer. However, a subset of colorectal cancer patients who have defective mismatch-repair (dMMR) pathway show resistance to 5-FU. Here, we demonstrate that the efficacy of 5-FU in dMMR colorectal cancer cells is largely dependent on the DNA base excision repair (BER) pathway. Downregulation of APE1, a key enzyme in the BER pathway, decreases IC

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCarbazolesChromatinColonic NeoplasmsDNA-(Apurinic or Apyrimidinic Site) LyaseDNA-Binding ProteinsDrug Resistance, NeoplasmFluorouracilHCT116 CellsHEK293 CellsHigh Mobility Group ProteinsHistone ChaperonesHumansMaleMiceAPEX1 protein, humanCarbazolesChromatinDNA-(Apurinic or Apyrimidinic Site) LyaseDNA-Binding ProteinsFluorouracilHigh Mobility Group ProteinsHistone ChaperonesSSRP1 protein, humanTranscriptional Elongation Factors

Identifiers

PMID31575655
PMCPMC6946866
OpenAlexW2979198871

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.