Evidence map›Paper›PMID 36658662›Full record

ArticleGenes and environment : the official journal of the Japanese Environmental Mutagen Society2023

Azaphilones produced by Penicillium maximae with their cell death-inducing activity on Adriamycin-treated cancer cell.

Takahiro Matsumoto, Erika Ohnishi, Takahiro Kitagawa, Masaya Okayama, Youhei Saito, Hayato Yoshikawa, Tomoe Ohta, Tatsusada Yoshida, Yuji Nakayama, Tetsushi Watanabe

Open access · goldAbstract read
In one paragraph

Article in Genes and environment : the official journal of the Japanese Environmental Mutagen Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
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

10 authors at 2 institutions in 1 country.

Takahiro MatsumotoKyoto Pharmaceutical University, 1 Misasagi-Shichono-cho, Yamashina-ku, 607-8412, Kyoto, Japan. tmatsumo@mb.kyoto-phu.ac.jp.
Erika OhnishiKyoto Pharmaceutical University, 1 Misasagi-Shichono-cho, Yamashina-ku, 607-8412, Kyoto, Japan.
Takahiro KitagawaKyoto Pharmaceutical University, 1 Misasagi-Shichono-cho, Yamashina-ku, 607-8412, Kyoto, Japan.
Masaya OkayamaKyoto Pharmaceutical University, 1 Misasagi-Shichono-cho, Yamashina-ku, 607-8412, Kyoto, Japan.
Youhei SaitoKyoto Pharmaceutical University, 1 Misasagi-Shichono-cho, Yamashina-ku, 607-8412, Kyoto, Japan.
Hayato YoshikawaKyoto Pharmaceutical University, 1 Misasagi-Shichono-cho, Yamashina-ku, 607-8412, Kyoto, Japan.
Tomoe OhtaFaculty of Pharmaceutical Sciences, Nagasaki International University, 2825-7 Huis Ten Bosch-Cho, 859-3298, Sasebo, Nagasaki, Japan.
Tatsusada YoshidaFaculty of Pharmaceutical Sciences, Nagasaki International University, 2825-7 Huis Ten Bosch-Cho, 859-3298, Sasebo, Nagasaki, Japan.
Yuji NakayamaKyoto Pharmaceutical University, 1 Misasagi-Shichono-cho, Yamashina-ku, 607-8412, Kyoto, Japan.
Tetsushi WatanabeKyoto Pharmaceutical University, 1 Misasagi-Shichono-cho, Yamashina-ku, 607-8412, Kyoto, Japan. watanabe@mb.kyoto-phu.ac.jp.
Kyoto Pharmaceutical University · JPNagasaki International University · JP

Funding

Japan Society for the Promotion of Science 20H03397
6 · The paper itself

Abstract

backgroundHeat shock proteins (Hsps) are overexpressed in several tumors and contribute to cell proliferation, metastasis, and anticancer drug resistance. Therefore, Hsp inhibitors have enhanced cytotoxicity as chemotherapeutic agents and may be effective with a reduced dosage for tumor therapy to avoid side effects.

resultsFour new azaphilones, maximazaphilones I-IV (1-4), and three known compounds (5-7) have been isolated from the airborne-derived fungus Penicillium maximae. Inhibitory effects of isolated compounds against induction of Hsp105 were evaluated by the luciferase assay system using Hsp105 promoter. In this assay, 2-4, 6, and 7 significantly inhibited hsp105 promoter activity without cytotoxicity. In addition, all isolated compounds except for 5 significantly induced the death of Adriamycin (ADR)-treated HeLa cells. Interestingly, 1-4, 6, and 7 didn't show anti-proliferative and cell death-inducing activity without ADR.

conclusionThis study revealed the chemical structures of maximazaphilones I-IV (1-4) and the potency of azaphilones may be useful for cancer treatment and reducing the dose of anticancer agents. In addition, one of the mechanisms of cell death-inducing activity for 2-4, 6, and 7 was suggested to be inhibitory effects of Hsp105 expression.

Indexed as

AdriamycinAzaphiloneFungusHeat shock proteinJKYM-AK1MaximazaphilonePenicillium maximaeTime-lapse imaging

Identifiers

PMID36658662
PMCPMC9850696
OpenAlexW4317436042

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.