Evidence map›Paper›PMID 31209282›Full record

ArticleScientific reports2019

Mechanistic study of PpIX accumulation using the JFCR39 cell panel revealed a role for dynamin 2-mediated exocytosis.

Yuya Kitajima, Takuya Ishii, Takeo Kohda, Masahiro Ishizuka, Kanami Yamazaki, Yumiko Nishimura, Tohru Tanaka, Shingo Dan, Motowo Nakajima

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 52 citations in OpenAlex.

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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 2 institutions in 1 country.

Yuya KitajimaSBI Pharmaceuticals Co., Ltd, Tokyo, Japan.
Takuya IshiiSBI Pharmaceuticals Co., Ltd, Tokyo, Japan.
Takeo KohdaSBI Pharmaceuticals Co., Ltd, Tokyo, Japan.
Masahiro IshizukaSBI Pharmaceuticals Co., Ltd, Tokyo, Japan.
Kanami YamazakiDivision of Molecular Pharmacology, Cancer Chemotherapy Center, Japan Foundation for Cancer Research, Tokyo, Japan.
Yumiko NishimuraDivision of Molecular Pharmacology, Cancer Chemotherapy Center, Japan Foundation for Cancer Research, Tokyo, Japan.
Tohru TanakaSBI Pharmaceuticals Co., Ltd, Tokyo, Japan.
Shingo DanDivision of Molecular Pharmacology, Cancer Chemotherapy Center, Japan Foundation for Cancer Research, Tokyo, Japan. sdan@jfcr.or.jp.
Motowo NakajimaSBI Pharmaceuticals Co., Ltd, Tokyo, Japan. motnakaj@sbigroup.co.jp.
SBI Pharmaceuticals (Japan) · JPJapanese Foundation For Cancer Research · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

5-aminolevulinic acid (5-ALA) has recently been employed for photodynamic diagnosis (ALA-PDD) and photodynamic therapy (ALA-PDT) of various types of cancer because hyperproliferating tumor cells do not utilize oxidative phosphorylation and do not efficiently produce heme; instead, they accumulate protoporphyrin IX (PpIX), which is a precursor of heme that is activated by violet light irradiation that results in the production of red fluorescence and singlet oxygen. The efficiencies of ALA-PDD and ALA-PDT depend on the efficient cellular uptake of 5-ALA and the inefficient excretion of PpIX. We employed the JFCR39 cell panel to determine whether tumor cells originating from different tissues can produce and accumulate PpIX. We also investigated cellular factors/molecules involved in PpIX excretion by tumor cells with the JFCR39 cell panel. Unexpectedly, the expression levels of ABCG2, which has been considered to play a major role in PpIX extracellular transport, did not show a strong correlation with PpIX excretion levels in the JFCR39 cell panel, although an ABCG2 inhibitor significantly increased intracellular PpIX accumulation in several tumor cell lines. In contrast, the expression levels of dynamin 2, which is a cell membrane-associated molecule involved in exocytosis, were correlated with the PpIX excretion levels. Moreover, inhibitors of dynamin significantly suppressed PpIX excretion and increased the intracellular levels of PpIX. This is the first report demonstrating the causal relationship between dynamin 2 expression and PpIX excretion in tumor cells.

Indexed as

Aminolevulinic AcidCell Line, TumorDynamin IIExocytosisHemeHumansMicroscopy, FluorescenceMitochondriaPhotochemotherapyPhotosensitizing AgentsProtoporphyrinsTrimethyl Ammonium CompoundsUltraviolet RaysAminolevulinic AcidDNM2 protein, humanDynamin IIHemePhotosensitizing Agentsprotoporphyrin IXProtoporphyrinstetradecyltrimethylammoniumTrimethyl Ammonium Compounds

Identifiers

PMID31209282
PMCPMC6572817
OpenAlexW2951540040

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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.