Evidence map›Paper›PMID 25822972›Full record

ArticlePloS one2015

The effect of iron ion on the specificity of photodynamic therapy with 5-aminolevulinic acid.

Maiko Hayashi, Hideo Fukuhara, Keiji Inoue, Taro Shuin, Yuichiro Hagiya, Motowo Nakajima, Tohru Tanaka, Shun-ichiro Ogura

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-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

18 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  6. Article
  7. Article
  8. Review
  9. Photodynamic Therapy for Bladder Cancers, A Focused ReviewPhotochemistry and photobiology · 2023
    Review
  10. Article
  11. Article
  12. Article
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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

8 authors at 3 institutions in 1 country.

Maiko HayashiGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259-B47, Nagatsuta-cho, Midori-ku, Yokohama, 226-8501, Japan.
Hideo FukuharaDepartment of Urology, Kochi Medical School, Kohasu, Oko-cho, Nankoku, Kochi, 783-8505, Japan.
Keiji InoueDepartment of Urology, Kochi Medical School, Kohasu, Oko-cho, Nankoku, Kochi, 783-8505, Japan.
Taro ShuinDepartment of Urology, Kochi Medical School, Kohasu, Oko-cho, Nankoku, Kochi, 783-8505, Japan.
Yuichiro HagiyaGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259-B47, Nagatsuta-cho, Midori-ku, Yokohama, 226-8501, Japan.
Motowo NakajimaSBI Pharma CO., LTD., Izumi Garden Tower 20F, 1-6-1, Roppongi Minato-ku, Tokyo, 106-6020, Japan.
Tohru TanakaSBI Pharma CO., LTD., Izumi Garden Tower 20F, 1-6-1, Roppongi Minato-ku, Tokyo, 106-6020, Japan.
Shun-ichiro OguraGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259-B47, Nagatsuta-cho, Midori-ku, Yokohama, 226-8501, Japan.
Kōchi University · JPTokyo Institute of Technology · JPSBI Pharmaceuticals (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, photodynamic therapy using 5-aminolevulinic acid (ALA-PDT) has been widely used in cancer therapy. ALA administration results in tumor-selective accumulation of the photosensitizer protoporphyrin IX (PpIX) via the heme biosynthetic pathway. Although ALA-PDT has selectivity for tumor cells, PpIX is accumulated into cultured normal cells to a small extent, causing side effects. The mechanism of tumor-selective PpIX accumulation is not well understood. The purpose of the present study was to identify the mechanism of tumor-selective PpIX accumulation after ALA administration. We focused on mitochondrial labile iron ion, which is the substrate for metabolism of PpIX to heme. We investigated differences in iron metabolism between tumor cells and normal cells and found that the amount of mitochondrial labile iron ion in cancer was lower than that in normal cells. This finding could be because of the lower expression of mitoferrins, which are the mitochondrial iron transporters. Accordingly, we added sodium ferrous citrate (SFC) with ALA as a source of iron. As a result, we observed the accumulation of PpIX only in tumor cells, and only these cells showed sensitivity to ALA-PDT. Taken together, these results suggest that the uptake abilities of iron ion into mitochondria play a key role in tumor-selective PpIX accumulation. Using SFC as a source of iron might thus increase the specificity of ALA-PDT effects.

Indexed as

Aminolevulinic AcidCation Transport ProteinsCell Line, TumorHemeHumansIronMCF-7 CellsMitochondriaPhotochemotherapyPhotosensitizing AgentsProtoporphyrinsSensitivity and SpecificityAminolevulinic AcidCation Transport ProteinsHemeIronPhotosensitizing Agentsprotoporphyrin IXProtoporphyrins

Identifiers

PMID25822972
PMCPMC4379089
OpenAlexW2060913055

What OpenQuestion holds

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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.