Evidence map›Paper›PMID 29522284›Full record

ArticleCancer medicine2018

Apoptin-derived peptide reverses cisplatin resistance in gastric cancer through the PI3K-AKT signaling pathway.

Danyang Zhou, Wenjing Liu, Songhe Liang, Banghao Sun, Anqi Liu, Zhongqi Cui, Xue Han, Lijie Yuan

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. The NaturalInternational journal of molecular sciences · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. [Myrislignan Induces Apoptosis in Gastric Cancer Cell Line Through PI3K/AKT Signaling Pathway].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2023
    Article
  8. Article
  9. Synergism of rMV-Hu191 with cisplatin to treat gastric cancer by acid sphingomyelinase-mediated apoptosis requiring integrity of lipid raft microdomains.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2021
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Danyang ZhouDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Daqing Campus, Daqing, Heilongjiang, 163319, China.ORCID 0000-0002-8698-1182
Wenjing LiuClinical Laboratory of Daqing People's Hospital Daqig, Helongjiang, 163310, China.
Songhe LiangDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Daqing Campus, Daqing, Heilongjiang, 163319, China.
Banghao SunDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Daqing Campus, Daqing, Heilongjiang, 163319, China.
Anqi LiuDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Daqing Campus, Daqing, Heilongjiang, 163319, China.
Zhongqi CuiDepartment of Clinical Laboratory Medicine, Shanghai Tenth People's Hospital of Tongji University, Shanghai, 200072, China.
Xue HanDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Daqing Campus, Daqing, Heilongjiang, 163319, China.
Lijie YuanDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Daqing Campus, Daqing, Heilongjiang, 163319, China.
Harbin Medical University · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of gastric cancer (GC) remains poor due to clinical drug resistance, and novel drugs are urgently needed. Apoptin-derived peptide (AdP) is an antitumor polypeptide constructed in our laboratory that has been used to combat cisplatin (CDDP) resistance in GC cells. MTT and colony-formation assays and Hoechst 33342 staining were used to measure the cytotoxicity of CDDP and AdP in GC cells. Cell apoptosis was measured using an Annexin-V-FITC/PI dual staining assay. Western blot analysis was conducted to detect the expression of proteins in the PI3K/AKT signaling pathway and resistance-related markers. AdP exerted a specific cytotoxic effect on GC cells and CDDP-resistant GC cells in a concentration- and time-dependent manner. AdP also suppressed cell invasion and migration. Additionally, AdP inhibited the expression of p85, AKT, p-p85, p-AKT, multidrug resistance 1 (MDR1), and aryl hydrocarbon nuclear translocator (ARNT) in the PI3K/AKT/ARNT signaling pathway, which promoted apoptosis and necrosis in GC cells. AdP promoted apoptosis in CDDP-resistant GC cells by suppressing the PI3K/AKT/ARNT signaling pathway and might be considered a candidate agent for the clinical treatment of cisplatin-resistant GC.

Indexed as

PeptidesAdultAgedAmino Acid SequenceAnimalsApoptosisBiomarkers, TumorCell Line, TumorCell SurvivalCisplatinDrug Resistance, NeoplasmFemaleHumansMaleMiceMiddle AgedBiomarkers, TumorCisplatinPeptidesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktApoptin-derived peptidecisplatin resistancegastric cancerPI3K/AKT/ARNT

Identifiers

PMID29522284
PMCPMC5911602
OpenAlexW2790977670

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.