Evidence map›Paper›PMID 34453238›Full record

ArticleJournal of medical ultrasonics (2001)2021

Low-intensity ultrasound inhibits melanoma cell proliferation in vitro and tumor growth in vivo.

Loreto B Feril, Kazuki Yamaguchi, Yurika Ikeda-Dantsuji, Yukihiro Furusawa, Yoshiaki Tabuchi, Ichiro Takasaki, Ryohei Ogawa, Zheng-Guo Cui, Katsuro Tachibana

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Article in Journal of medical ultrasonics (2001), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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 4 institutions in 1 country.

Loreto B FerilDepartment of Anatomy, Fukuoka University School of Medicine, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Kazuki YamaguchiDepartment of Anatomy, Fukuoka University School of Medicine, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Yurika Ikeda-DantsujiDepartment of Chemotherapy and Mycosis, National Institute of Infectious Diseases, Tokyo, Japan.
Yukihiro FurusawaDepartment of Liberal Arts and Sciences, Toyama Prefecture University, Toyama, 939-0398, Japan.
Yoshiaki TabuchiDivision of Molecular Genetics Research, Life Science Research Center, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
Ichiro TakasakiDivision of Molecular Genetics Research, Life Science Research Center, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
Ryohei OgawaDepartment of Radiological Sciences, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
Zheng-Guo CuiDepartment of Environmental Science, School of Medical Science, University of Fukui, Fukui, 910-1193, Japan.
Katsuro TachibanaDepartment of Anatomy, Fukuoka University School of Medicine, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan. k-tachi@fukuoka-u.ac.jp.ORCID http://orcid.org/0000-0002-8514-696X
University of Toyama · JPFukuoka University · JPNational Institute of Infectious Diseases · JPUniversity of Fukui · JP

Funding

Japan Society for the Promotion of Science 18800075
6 · The paper itself

Abstract

purposeTo determine the effect of low-intensity ultrasound on cancer cell proliferation in vitro and tumor growth in vivo.

methodsIn vitro, several cancer cell lines were exposed to low-intensity ultrasound at 0.11 W/cm

resultsIn vitro, C32 cell growth was inhibited, attaining 43.2% inhibition on the 3rd day. In vivo, tumor growth was significantly inhibited, with the treated tumors exhibiting 2.7-fold slowed tumor growth vs. untreated tumors at week 2. Such inhibition was not associated with increased cell death. Several genes related to the cell cycle and proliferation were among those significantly regulated.

conclusionThese findings highlight the potential of low-intensity ultrasound to inhibit tumor growth in a noninvasive, safe, and easy-to-administer way. In addition, this may suggest that the mechanical stress induced by ultrasound on C32 cells may have affected the intrinsic biomolecular mechanism related to the cell growth of this particular cell line. Further research is needed to identify which of the regulated genes played key roles in growth inhibition.

Indexed as

MelanomaAnimalsCell Line, TumorCell ProliferationMiceCancerGene regulationGrowth inhibitionMelanomaUltrasound

Identifiers

PMID34453238
OpenAlexW3193636725

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.