Evidence map›Paper›PMID 27123146›Full record

ArticleOncology letters2016

Synergistic antitumor activity of gemcitabine combined with triptolide in pancreatic cancer cells.

Zhixin Qiao, Min He, M U He, Weijing Li, Xuanlin Wang, Yanbing Wang, Qiyuan Kuai, Changlan Li, Suping Ren, Qun Yu

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.8field-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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Therapeutic applications and delivery systems for triptolide.Drug delivery and translational research · 2020
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
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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

10 authors at 1 institution in 1 country.

Zhixin QiaoDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China; Medical Research Center, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, P.R. China.
Min HeDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China.
M U HeDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China; College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100022, P.R. China.
Weijing LiDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China.
Xuanlin WangDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China.
Yanbing WangDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China; College of Life Sciences, Jilin University, Changchun, Jilin 130012, P.R. China.
Qiyuan KuaiDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China.
Changlan LiDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China; College of Life Science, Northeast Normal University, Changchun, Jilin 130024, P.R. China.
Suping RenDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China.
Qun YuDepartment of Blood Products and Substitutes, Beijing Institute of Transfusion Medicine, Beijing 100850, P.R. China.
Guangzhou Blood Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is a fatal human malignancy associated with an exceptionally poor prognosis. Novel therapeutic strategies are urgently required to treat this disease. In addition to immunosuppressive activity, triptolide possesses strong antitumor activity and synergistically enhances the antitumor activities of conventional chemotherapeutic drugs in preclinical models of pancreatic cancer. The present study investigated the antitumor effects of triptolide in pancreatic cancer cells, either in combination with gemcitabine, or alone. The pancreatic cancer BxPC-3 and PANC-1 cell lines were treated with triptolide, which resulted in time- and dose-dependent growth arrest. When incorporated into a sequential schedule, triptolide synergistically increased gemcitabine-induced cell growth inhibition and apoptosis, in addition to the cooperative regulation of B-cell lymphoma 2 family proteins and loss of mitochondrial membrane potential. Furthermore, triptolide enhanced gemcitabine-induced S phase arrest and DNA double-strand breaks, possibly through checkpoint kinase 1 suppression. The results of the present study suggest that triptolide has therapeutic potential for the treatment of pancreatic cancer, particularly when administered in combination with gemcitabine.

Indexed as

apoptosisDNA damagegemcitabinepancreatic cancertriptolide

Identifiers

PMID27123146
PMCPMC4840967
OpenAlexW2334309804

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.