Evidence map›Paper›PMID 29434949›Full record

ArticleOncology letters2018

Carnosic acid, an inducer of NAD(P)H quinone oxidoreductase 1, enhances the cytotoxicity of β-lapachone in melanoma cell lines.

Nobuyuki Arakawa, Ayaka Okubo, Shinji Yasuhira, Kazuhiro Takahashi, Hiroo Amano, Toshihide Akasaka, Tomoyuki Masuda, Masahiko Shibazaki, Chihaya Maesawa

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. The dual role of Nrf2 in melanoma: a systematic review.BMC molecular and cell biology · 2023
    Pooled it
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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.

Nobuyuki ArakawaDepartment of Tumor Biology, Institute of Biomedical Science, Iwate Medical University, Iwate 028-8505, Japan.
Ayaka OkuboDepartment of Tumor Biology, Institute of Biomedical Science, Iwate Medical University, Iwate 028-8505, Japan.
Shinji YasuhiraDepartment of Tumor Biology, Institute of Biomedical Science, Iwate Medical University, Iwate 028-8505, Japan.
Kazuhiro TakahashiDepartment of Dermatology, Iwate Medical University, Iwate 028-3694, Japan.
Hiroo AmanoDepartment of Dermatology, Iwate Medical University, Iwate 028-3694, Japan.
Toshihide AkasakaDivision of Dermatology, Kitakami Saiseikai Hospital, Iwate 024-8506, Japan.
Tomoyuki MasudaDepartment of Pathology, School of Medicine, Iwate Medical University, Iwate 028-3694, Japan.
Masahiko ShibazakiDepartment of Tumor Biology, Institute of Biomedical Science, Iwate Medical University, Iwate 028-8505, Japan.
Chihaya MaesawaDepartment of Tumor Biology, Institute of Biomedical Science, Iwate Medical University, Iwate 028-8505, Japan.
Iwate Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NAD(P)H quinone oxidoreductase 1 (NQO1)-dependent antitumor drugs such as β-lapachone (β-lap) are attractive candidates for cancer chemotherapy because several tumors exhibit higher expression of NQO1 than adjacent tissues. Although the association between NQO1 and β-lap has been elucidated, the effects of a NQO1-inducer and β-lap used in combination remain to be clarified. It has previously been reported that melanoma cell lines have detectable levels of NQO1 expression and are sensitive to NQO1-dependent drugs such as 17-allylamino-17-demethoxygeldanamycin. The present study was conducted to investigate the involvement of NQO1 in β-lap-mediated toxicity and the utility of combination treatment with a NQO1-inducer and β-lap in malignant melanoma cell lines. Decreased expression or inhibition of NQO1 caused these cell lines to become less sensitive to β-lap, indicating a requirement of NQO1 activity for β-lap-mediated toxicity. Of note was that carnosic acid (CA), a compound extracted from rosemary, was able to induce further expression of NQO1 through NF-E2 related factor 2 (NRF2) stabilization, thus significantly enhancing the cytotoxicity of β-lap in all of the melanoma cell lines tested. Taken together, the data presented in the current study indicated that the NRF2-NQO1 axis may have potential value as a therapeutic target in malignant melanoma to improve the rate of clinical response to NQO1-dependent antitumor drugs.

Indexed as

carnosic acidmelanomaNAD(P)H quinone oxidoreductase 1NF-E2 related factor 2β-lapachone

Identifiers

PMID29434949
PMCPMC5777343
OpenAlexW2775483233

What OpenQuestion holds

Textmetadata
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.