Evidence map›Paper›PMID 25985143›Full record

ReviewCancer biology & therapy2015

The interplay between DNA repair and autophagy in cancer therapy.

Dan Zhang, Bo Tang, Xia Xie, Yu-Feng Xiao, Shi-Ming Yang, Jian-Wei Zhang

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

73 citing papers in PubMed, 136 citations in OpenAlex.

  1. Review
  2. Article
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  12. Review
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  16. miR-1246-overexpressing exosomes improve UVB-induced photoaging by activating autophagy via suppressing GSK3β.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2024
    Article
  17. Review
  18. Article
  19. Article
  20. Review

13 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Dan Zhanga Department of Gastroenterology; Xinqiao Hospital; Third Military Medical University ; Chongqing , China.
Bo Tang
Xia Xie
Yu-Feng Xiao
Shi-Ming Yang
Jian-Wei Zhang
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA is the prime target of anticancer treatments. DNA damage triggers a series of signaling cascades promoting cellular survival, including DNA repair, cell cycle arrest, and autophagy. The elevated basal and/or stressful levels of both DNA repair and autophagy observed in tumor cells, in contrast to normal cells, have been identified as the most important drug-responsive programs that impact the outcome of anticancer therapy. The exact relationship between DNA repair and autophagy in cancer cells remains unclear. On one hand, autophagy has been shown to regulate some of the DNA repair proteins after DNA damage by maintaining the balance between their synthesis, stabilization, and degradation. One the other hand, some evidence has demonstrated that some DNA repair molecular have a crucial role in the initiation of autophagy. In this review, we mainly discuss the interplay between DNA repair and autophagy in anticancer therapy and expect to enlighten some effective strategies for cancer treatment.

Indexed as

DNA DamageDNA RepairSignal TransductionApoptosisAutophagyCell SurvivalHumansModels, GeneticNeoplasmsAMPK, adenosine monophosphate-activated protein kinaseanticancer therapyapoptosisATG5, autophagy-related gene 5ATM, ataxia-telangiectasia mutatedATR, ATM and Rad3-relatedautophagyBER, base excision repaircell cycle arrestChk1, check-point kinase 1Chk2, check-point kinase 2DDR, DNA damage responseDNA damageDNA damage responseDNA-PKcs, DNA-dependent protein kinase catalytic subunitDNA repairDSBs, double-strand breaksHDAC, histone deacetylasesHR, homologous recombinationIR, ionizing radiationMGMT, O6 methylguanine –DNA methyltransferaseMMR, mismatch repairMRN, Mre11-Rad50-Nbs1mTOR, mammalian target of rapamycinNER, nucleotide excision recombinationNHEJ, non-homologous end joiningOGG1, 8-oxoguannine DNA glycosidasePARP-1, poly (ADP-ribose) polymerase 1PI3K, phosphoinositide 3-kinasePML, promyelocytic leukemiaSSBs, single-strand breakTMZ, temozolomideTSC2, tuberous sclerosis complex 2γ-H2AX, phosphorylated histone

Identifiers

PMID25985143
PMCPMC4622693
OpenAlexW2273909154

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.