Evidence map›Paper›PMID 29901163›Full record

ArticleOncology reports2018

Norcantharidin reverses cisplatin resistance and inhibits the epithelial mesenchymal transition of human non‑small lung cancer cells by regulating the YAP pathway.

Dan Jin, Yan Wu, Cuijie Shao, Yong Gao, Deqiang Wang, Jiwei Guo

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Oncology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.4field-weighted citation impact, top 12% 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, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. The Roles of CCN1/CYR61 in Pulmonary Diseases.International journal of molecular sciences · 2020
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. The Ambivalent Function of YAP in Apoptosis and Cancer.International journal of molecular sciences · 2018
    Review
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Dan JinDepartment of Pain Medicine, Binzhou Medical University Hospital, Binzhou, Shandong 256603, P.R. China.
Yan WuCancer Research Institute, Binzhou Medical University Hospital, Binzhou, Shandong 256603, P.R. China.
Cuijie ShaoDepartment of Pain Medicine, Binzhou Medical University Hospital, Binzhou, Shandong 256603, P.R. China.
Yong GaoDepartment of Pain Medicine, Binzhou Medical University Hospital, Binzhou, Shandong 256603, P.R. China.
Deqiang WangDepartment of Pain Medicine, Binzhou Medical University Hospital, Binzhou, Shandong 256603, P.R. China.
Jiwei GuoCancer Research Institute, Binzhou Medical University Hospital, Binzhou, Shandong 256603, P.R. China.
Binzhou University · CNBinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non‑small cell lung cancer (NSCLC) accounts for >80% of all lung cancer cases, which are the leading cause of cancer‑related mortality worldwide. The clinical efficacy of available therapies for NSCLC is often limited due to the development of resistance to anticancer drugs, particularly to cisplatin (DDP). Norcantharidin (NCTD) is a traditional Chinese medicine used in the treatment of many types of cancer, to which patients do not develop resistance. The aim of the present study was to examine the potential synergistic effects of NCTD and DPP on the viability of the the DDP‑resistant NSCLC cell line, A549/DDP. We further explored the potential underlying mechanisms by examining the expression of the oncogene, Yes-associated protein 1 (YAP), whose activation was recently found to be associated with drug resistance. We further examined a series of human lung cancer cell lines and tissues from patients with lung cancer, which revealed that YAP activation contributed to lung cancer initiation, progression and metastasis, and was associated with a poor prognosis, and confering resistance against targeted therapies. Moreover, YAP expression was evaluated in the A549/DDP cells treated with NCTD, DDP, or both drugs. The combined treatment significantly sensitized the A549/DDP cells to DDP‑induced growth inhibition by reducing YAP promoter activity (based on transcriptional expression) and the expression of its target genes, connective tissue growth factor (CTGF) and cysteine rich angiogenic inducer 61 (CYR61). Furthermore, compared to the individual treatments, combined treatment increased cell apoptosis and senescence, and decreased epithelial‑to‑mesenchymal transition and the cell migratory and invasive ability. On the whole, our data indicate that the application of NCTD with reverses DDP resistance and thus, this combined treatment may have promising prospects for use in improving the outcome of patients with NSCLC.

Indexed as

A549 CellsAntineoplastic AgentsApoptosisBridged Bicyclo Compounds, HeterocyclicCarcinoma, Non-Small-Cell LungCell Cycle ProteinsCell Line, TumorCell ProliferationCisplatinConnective Tissue Growth FactorDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFemaleHumansLung NeoplasmsMaleAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicCell Cycle ProteinsCisplatinConnective Tissue Growth FactornorcantharidinNuclear ProteinsTranscription FactorsYY1AP1 protein, human

Identifiers

PMID29901163
PMCPMC6072289
OpenAlexW2808118122

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.