Evidence map›Paper›PMID 37414938›Full record

ArticleThe Journal of antibiotics2023

Rubiflavin G, photorubiflavin G, and photorubiflavin E: Novel pluramycin derivatives from Streptomyces sp. W2061 and their anticancer activity against breast cancer cells.

Byeongsan Lee, Ga-Eun Lee, Gwi Ja Hwang, Kyung Taek Heo, Jae Kyoung Lee, Jun-Pil Jang, Bang Yeon Hwang, Jae-Hyuk Jang, Yong-Yeon Cho, Young-Soo Hong

Abstract read
PubMed Publisher
In one paragraph

Article in The Journal of antibiotics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Natural products with γ-pyrone scaffold from Streptomyces.Applied microbiology and biotechnology · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. 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 3 institutions in 1 country.

Byeongsan LeeChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Korea.
Ga-Eun LeeCollege of Pharmacy, The Catholic University of Korea, Bucheon-si, Gyeonggi-do, 14662, Korea.
Gwi Ja HwangChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Korea.
Kyung Taek HeoChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Korea.
Jae Kyoung LeeChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Korea.
Jun-Pil JangChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Korea.
Bang Yeon HwangCollege of Pharmacy, Chungbuk National University, Cheongju, 28160, Korea.
Jae-Hyuk JangChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Korea. jangjh@kribb.re.kr.ORCID http://orcid.org/0000-0002-4363-4252
Yong-Yeon ChoCollege of Pharmacy, The Catholic University of Korea, Bucheon-si, Gyeonggi-do, 14662, Korea. yongyeon@catholic.ac.kr.
Young-Soo HongChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Korea. hongsoo@kribb.re.kr.ORCID http://orcid.org/0000-0001-7768-2239
Korea Research Institute of Bioscience and Biotechnology · KRCatholic University of Korea · KRChungbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pluramycin family of antibiotics comprises angucycline compounds derived from actinomycetes that possess anticancer and antibacterial properties. Pluramycins are structurally characterized by two aminoglycosides linked by a carbon-carbon bond next to the γ-pyrone angucycline backbone. Kidamycins (3, 4) and rubiflavins (6-9) were screened through liquid chromatography-mass spectrometry analysis of the crude extracts of Streptomyces sp. W2061, which was cultured in complex media under phosphate-limiting conditions. Newly isolated rubiflavin G (7) and photoactivated compounds (8, 9) were characterized using exhaustive 1D and 2D nuclear magnetic resonance analysis. The cytotoxicity of kidamycin (3), photokidamycin (4), and photorubiflavin G (8) was determined using two human breast cancer cell lines-MCF7 and MDA-MB-231. Compared to MCF7 cells, MDA-MB-231 cells were more sensitive to the active compounds, and photokidamycin (4) considerably inhibited MCF7 and MDA-MB-231 cell growth (IC

Indexed as

Antineoplastic AgentsBreast NeoplasmsStreptomycesAminoglycosidesAnti-Bacterial AgentsCarbonCell Line, TumorFemaleHumansAminoglycosidesAnti-Bacterial AgentsAntineoplastic AgentsCarbonpluramycinrubiflavin

Identifiers

PMID37414938
OpenAlexW4383369703

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.