Evidence map›Paper›PMID 26530267›Full record

ArticleJournal of neuro-oncology2016

Temozolomide reverses doxorubicin resistance by inhibiting P-glycoprotein in malignant glioma cells.

Rong Zhang, Ryuta Saito, Ichiyo Shibahara, Shinichiro Sugiyama, Masayuki Kanamori, Yukihiko Sonoda, Teiji Tominaga

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Epilepsy in Patients with Gliomas.Neurologia medico-chirurgica · 2024
    Review
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  8. Review
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  10. Article
  11. Article
  12. Article
  13. Glycosylation Changes in Brain Cancer.ACS chemical neuroscience · 2018
    Review
  14. Article
  15. Article
  16. 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

7 authors at 1 institution in 1 country.

Rong ZhangDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-cho, Aobaku, Sendai, 980-8574, Miyagi, Japan.
Ryuta SaitoDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-cho, Aobaku, Sendai, 980-8574, Miyagi, Japan. ryuta@nsg.med.tohoku.ac.jp.
Ichiyo ShibaharaDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-cho, Aobaku, Sendai, 980-8574, Miyagi, Japan.
Shinichiro SugiyamaDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-cho, Aobaku, Sendai, 980-8574, Miyagi, Japan.
Masayuki KanamoriDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-cho, Aobaku, Sendai, 980-8574, Miyagi, Japan.
Yukihiko SonodaDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-cho, Aobaku, Sendai, 980-8574, Miyagi, Japan.
Teiji TominagaDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-cho, Aobaku, Sendai, 980-8574, Miyagi, Japan.
Tohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Temozolomide is a standard chemotherapy agent for malignant gliomas, but the efficacy is still not satisfactory. Therefore, combination chemotherapy using temozolomide with other anti-tumor compounds is now under investigation. Here we studied the mechanism of the synergistic anti-tumor effect achieved by temozolomide and doxorubicin, and elucidated the inhibitory effect of temozolomide on P-glycoprotein (P-gp). Temozolomide significantly enhanced sensitivity to P-gp substrate in glioma cells, particularly in P-gp-overexpressed cells. Synergetic effects, as determined by isobologram analysis, were observed by combining temozolomide and doxorubicin. Subsequently, flow cytometry was utilized to assess the intracellular retention of doxorubicin in cells treated with doxorubicin with or without temozolomide. Temozolomide significantly increased the accumulation of doxorubicin in these cells. The P-gp adenosine triphosphatase (ATPase) assay showed that temozolomide inhibited the ATPase activity of P-gp. In addition, temozolomide combined with doxorubicin significantly prolonged the survival of 9L intracranial allografted glioma-bearing rats compared to single agent treatment. Collectively, our findings suggest that temozolomide can reverse doxorubicin resistance by directly affecting P-gp transport activity. Combination chemotherapy using temozolomide with other agents may be effective against gliomas in clinical applications.

Indexed as

Drug Resistance, NeoplasmAdenosine TriphosphatasesAnimalsAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1Brain NeoplasmsCell Line, TumorDacarbazineDoxorubicinDrug Therapy, CombinationGliomaHumansRatsSurvival AnalysisTemozolomideAdenosine TriphosphatasesAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1DacarbazineDoxorubicinTemozolomideBrain tumorChemotherapyDoxorubicinP-glycoproteinTemozolomide

Identifiers

PMID26530267
OpenAlexW1929868825

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.