Evidence map›Paper›PMID 27813497›Full record

ArticleOncotarget2016

Serum APE1 as a predictive marker for platinum-based chemotherapy of non-small cell lung cancer patients.

Shiheng Zhang, Le He, Nan Dai, Wei Guan, Jinlu Shan, Xueqin Yang, Zhaoyang Zhong, Yi Qing, Feng Jin, Chuan Chen and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 47 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. A GMR enzymatic assay for quantifying nuclease and peptidase activity.Frontiers in bioengineering and biotechnology · 2024
    Article
  11. Article
  12. The therapeutic potential of exosomes in lung cancer.Cellular oncology (Dordrecht, Netherlands) · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. APE1 controls DICER1 expression in NSCLC through miR-33a and miR-130b.Cellular and molecular life sciences : CMLS · 2022
    Article
  17. Observational
  18. Review
  19. Article
  20. 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

17 authors at 5 institutions in 3 countries.

Shiheng ZhangCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Le HeCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Nan DaiCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Wei GuanCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Jinlu ShanCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Xueqin YangCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Zhaoyang ZhongCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Yi QingCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Feng JinCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Chuan ChenCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Yuxin YangCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Hongyi WangDepartment of Pathology, Baylor University Medical Center, Dallas, TX 75246, USA.
Laura BaughDepartment of Pathology, Baylor University Medical Center, Dallas, TX 75246, USA.
Gianluca TellLaboratory of Molecular Biology and DNA repair, Department of Medical and Biological Sciences, University of Udine, Udine 33100, Italy.
David M WilsonLaboratory of Molecular Gerontology, National Institute on Aging, Intramural Research Program, National Institutes of Health, Baltimore, MD 21224, USA.
Mengxia LiCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Dong WangCancer Center of Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Army Medical University · CNDaping Hospital · CNBaylor University Medical Center · USNational Institute on Aging · USUniversity of Udine · IT

Funding

Base Excision DNA Repair in Disease Susceptibility and TreatmentZIAAG000750 · NIA · NATIONAL INSTITUTE ON AGING · PI BOHR, VILHELM A · 2009 to 2019
$5.4M
6 · The paper itself

Abstract

purposeTo define the role of the DNA repair protein apurinic/apyrimidinic endonuclease 1 (APE1) in predicting the prognosis and chemotherapeutic response of non-small cell lung cancer patients receiving platinum-containing chemotherapy.

resultsOur investigations found that serum APE1 level was significantly elevated in 229 of 412 NSCLC patients and correlated with its level in tissue (r2 = 0.639, p < 0.001). The elevated APE1 level in both tissue and serum of patients prior to chemotherapy was associated with worse progression-free survival (HR: 2.165, p < 0.001, HR: 1.421, p = 0.012), but not with overall survival. After 6 cycles of chemotherapy, a low APE1 serum level was associated with better overall survival (HR: 0.497, p = 0.010). EXPERIMENTAL

designWe measured APE1 protein levels in biopsy tissue from 172 NSCLC patients and sera of 412 NSCLC patients receiving platinum-based chemotherapy by immunohistochemistry and a newly established sensitive and specific enzyme-linked immunosorbent assay, respectively. APE1 levels in sera of 523 healthy donors were also determined as control.

conclusionsOur studies indicate that APE1 is a biomarker for predicting prognosis and therapeutic efficacy in NSCLC. The chemotherapy-naïve serum APE1 level, which correlated with its tissue level inversely associated with progression-free survival of platinum-containing doublet chemotherapy, whereas post-treatment serum APE1 level was inversely associated with overall survival.

Indexed as

Biomarkers, TumorAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungDNA-(Apurinic or Apyrimidinic Site) LyaseEnzyme-Linked Immunosorbent AssayFemaleGene ExpressionHumansLung NeoplasmsMaleMiddle AgedNeoplasm StagingPlatinumAPEX1 protein, humanBiomarkers, TumorDNA-(Apurinic or Apyrimidinic Site) LyasePlatinumAPE1biomarkerchemotherapyNSCLC

Identifiers

PMID27813497
PMCPMC5340230
OpenAlexW2549008179

What OpenQuestion holds

Textmetadata
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.