Evidence map›Paper›PMID 34329742›Full record

ArticleCancer letters2021

PCNA inhibition enhances the cytotoxicity of β-lapachone in NQO1-Positive cancer cells by augmentation of oxidative stress-induced DNA damage.

Xiaolin Su, Jiangwei Wang, Lingxiang Jiang, Yaomin Chen, Tao Lu, Marc S Mendonca, Xiumei Huang

Open access · bronzeAbstract read
In one paragraph

Article in Cancer letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  3. Real-time IncuCyteBio-protocol · 2025
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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

7 authors at 3 institutions in 1 country.

Xiaolin SuDepartment of Biochemistry and Molecular Biology, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Jiangwei WangDepartment of Radiation Oncology, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Lingxiang JiangDepartment of Radiation Oncology, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Yaomin ChenIndiana University Health Pathology Laboratory, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Tao LuDepartment of Pharmacology and Toxicology, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Marc S MendoncaDepartment of Radiation Oncology, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Xiumei HuangDepartment of Radiation Oncology, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, IN, 46202, USA. Electronic address: xiuhuang@iu.edu.
Indiana University – Purdue University Indianapolis · USIndiana University Health · USIndiana University School of Medicine

Funding

Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Sara K Quinney · 1999 to 2026
$59.3M
Targeting NQO1+ tumor to trigger innate and adaptive immunityR01CA240952 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI HUANG, XIUMEI · 2020 to 2024
$2.1M
Tumor-selective use of PARP inhibitors against NQO1+ nonsmall cell lung cancerR01CA221158 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HUANG, XIUMEI, MOTEA, EDWARD AYSON · 2017 to 2022
$1.9M
Tumor-selective radiosensitization of NSCLC using NQO1 bioactivatable drugsR01CA224493 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI HUANG, XIUMEI · 2018 to 2022
$1.8M
NCI NIH HHS P30 CA082709NCI NIH HHS R01 CA221158NCI NIH HHS R01 CA224493NCI NIH HHS R01 CA240952
6 · The paper itself

Abstract

β-Lapachone is a classic quinone-containing antitumor NQO1-bioactivatable drug that directly kills NQO1-overexpressing cancer cells. However, the clinical applications of β-lapachone are primarily limited by its high toxicity and modest lethality. To overcome this side effect and expand the therapeutic utility of β-lapachone, we demonstrate the effects of a novel combination therapy including β-lapachone and the proliferating cell nuclear antigen (PCNA) inhibitor T2 amino alcohol (T2AA) on various NQO1

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Cycle CheckpointsCell Line, TumorCell SurvivalDNA DamageDNA RepairFemaleG1 PhaseHumansMCF-7 CellsMiceMice, Inbred C57BLNAD(P)H Dehydrogenase (Quinone)NaphthoquinonesAntineoplastic Agentsbeta-lapachoneNAD(P)H Dehydrogenase (Quinone)NaphthoquinonesNQO1 protein, humanPCNA protein, humanProliferating Cell Nuclear AntigenReactive Oxygen SpeciesCombination chemotherapyNQO1PCNAT2AAβ-Lapachone

Identifiers

PMID34329742
PMCPMC8403654
OpenAlexW3185233273

What OpenQuestion holds

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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.