Evidence map›Paper›PMID 15375375›Full record

ArticleCancer gene therapy2004

Reversal of P-glycoprotein-mediated multidrug resistance with small interference RNA (siRNA) in leukemia cells.

Zhi Peng, Zhijian Xiao, Yi Wang, Peng Liu, Yinglin Cai, Shihong Lu, Wenli Feng, Zhong Chao Han

Abstract read
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In one paragraph

Article in Cancer gene therapy, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Reversal of Multidrug Resistance in an Epirubicin-Resistant Gastric Cancer Cell SublineAsian Pacific journal of cancer prevention : APJCP · 2018
    Article
  3. Effects ofOncology letters · 2018
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. 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

8 authors at 2 institutions in 1 country.

Zhi PengThe Faculty of Laboratory Medicine, Chongqing Medical University, Chongqing, China.
Zhijian Xiao
Yi Wang
Peng Liu
Yinglin Cai
Shihong Lu
Wenli Feng
Zhong Chao Han
Chinese Academy of Medical Sciences & Peking Union Medical College · CNChongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The multidrug resistance (MDR) mediated by P-glycoprotein (P-gp), the MDR1 gene product, is one of the major obstacles in leukemia treatment. The present study was designed to explore a MDR1-targeted small interfering RNA (si-MDR1) approach for reversal of P-gp-mediated MDR in the MDR human leukemia cell line k562/A02. It was found that si-MDR1 significantly inhibited MDR1 expression at both mRNA and protein levels. Depletion of MDR1 by si-MDR1 correlated with the increased sensitivity of the cells to cytotoxic agents and with the enhanced intracellular retention of daunorubicin (DNR). One base-pair mutated control (si-MDR1-Mut) lost the effect of si-MDR1 on both the degradation of mdr1 mRNA and the reduction of P-gp expression. These findings indicate that siRNA specifically and efficiently interferes with the expression of mdr1 and could be used as a molecularly defined therapeutic approach for MDR in the treatment of leukemia.

Indexed as

ATP Binding Cassette Transporter, Subfamily B, Member 1Base SequenceBlotting, WesternDaunorubicinDNA PrimersFlow CytometryHumansK562 CellsLeukemiaReverse Transcriptase Polymerase Chain ReactionRNA, Small InterferingATP Binding Cassette Transporter, Subfamily B, Member 1DaunorubicinDNA PrimersRNA, Small Interfering

Identifiers

PMID15375375
OpenAlexW2068562307

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.