Evidence map›Paper›PMID 31001120›Full record

ArticleFrontiers in pharmacology2019

Zinc-Doped Copper Oxide Nanocomposites Inhibit the Growth of Pancreatic Cancer by Inducing Autophagy Through AMPK/mTOR Pathway.

Xiao Li, Huanli Xu, Cong Li, Gan Qiao, Ammad Ahmad Farooqi, Aharon Gedanken, Xiaohui Liu, Xiukun Lin

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Cu-doped TiOJournal of nanobiotechnology · 2023
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Preparation and Characterization of Magnetic FeMaterials (Basel, Switzerland) · 2019
    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

8 authors at 3 institutions in 3 countries.

Xiao LiDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Huanli XuDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Cong LiDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Gan QiaoDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Ammad Ahmad FarooqiLaboratory for Translational Oncology and Personalized Medicine, Rashid Latif Medical College (RLMC), Lahore, Pakistan.
Aharon GedankenCenter for Advanced Materials and Nanotechnology, Bar-Ilan University, Ramat Gan, Israel.
Xiaohui LiuDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Xiukun LinDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Capital Medical University · CNBar-Ilan University · ILRashid Latif Medical College · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zinc doped copper oxide nanocomposites (Zn-CuO NPs) is a novel doped metal nanomaterial synthesized by our group using the sonochemical method. Our previous studies have shown that Zn-CuO NPs could inhibit cancer cell proliferation by inducing apoptosis via ROS-mediated pathway. In the present study, we studied the anticancer effect of Zn-CuO NPs on human pancreatic cancer cells. MTS assay revealed that Zn-CuO NPs was able to inhibit cancer cell growth. TEM, flow cytometry and fluorescence microscope analysis showed that Zn-CuO NPs induced autophagy significantly; the number of autophagosomes increased obviously in cells treated with Zn-CuO NPs. Western blot analysis revealed that treatment with the NPs resulted in activation of AMPK/mTOR pathway in both AsPC-1 and MIA Paca-2 cells in dose dependent manners. Moreover, in the presence of AMPK activator AMPKinone, the protein level of p-AMPK, p-ULK1, Beclin-1 and LC3-II/LC3-I increased, while the protein expression of p-AMPK, p-ULK1, Beclin-1 and LC3-II/LC3-I decreased in the presence of AMPK inhibitor Compound C.

Indexed as

AMPKautophagyin vivo activitypancreatic cancerzinc doped copper oxide nanocomposites

Identifiers

PMID31001120
PMCPMC6454023
OpenAlexW2923196661

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.