Evidence map›Paper›PMID 36102296›Full record

ArticleInternational journal of molecular medicine2022

Dual roles of oxostephanine as an Aurora kinase inhibitor and angiogenesis suppressor.

Thu-Hien Thi Tran, Le-Duy Ba Vu, Huy Quoc Nguyen, Hanh Bich Pham, Xuan-Phuong Thi Do, Uyen Thi Trang Than, Thu-Huong Thi Pham, Linh Dieu Do, Kim-Van Thi Le, Thao Phuong Nguyen and 1 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
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

11 authors at 6 institutions in 1 country.

Thu-Hien Thi Tran *Department of Pharmacognosy, Vietnam University of Traditional Medicine, Hanoi 10000, Vietnam.
Le-Duy Ba Vu *Department of Cell Biology, Faculty of Biology, VNU University of Science, Vietnam National University, Hanoi 10000, Vietnam.
Huy Quoc NguyenDepartment of Pharmacognosy, Vietnam University of Traditional Medicine, Hanoi 10000, Vietnam.
Hanh Bich PhamDepartment of Cell Biology, Faculty of Biology, VNU University of Science, Vietnam National University, Hanoi 10000, Vietnam.
Xuan-Phuong Thi DoDepartment of Cell Biology, Faculty of Biology, VNU University of Science, Vietnam National University, Hanoi 10000, Vietnam.
Uyen Thi Trang ThanCenter of Applied Sciences, Regenerative Medicine and Advance Technologies, Vinmec Healthcare System, Hanoi 10000, Vietnam.
Thu-Huong Thi PhamThe Key Laboratory of Enzyme and Protein Technology, VNU University of Science, Vietnam National University, Hanoi 10000, Vietnam.
Linh Dieu DoDepartment of Cell Biology, Faculty of Biology, VNU University of Science, Vietnam National University, Hanoi 10000, Vietnam.
Kim-Van Thi LeFaculty of Apothecary, National Institute of Medicinal Materials, Hanoi 10000, Vietnam.
Thao Phuong NguyenInstitute of Marine Biochemistry, Vietnam Academy of Science and Technology, Hanoi 10000, Vietnam.
My-Nhung Thi HoangDepartment of Cell Biology, Faculty of Biology, VNU University of Science, Vietnam National University, Hanoi 10000, Vietnam.
Vietnam National University, Hanoi · VNVNU University of Science · VNViet Nam University Of Traditional Medicine · VNNational Institute of Nutrition · VNVietnam Academy of Science and Technology · VNVinmec International Hospital · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Aurora kinases, including Aurora A, B and C, play critical roles in cell division. They have been found overexpressed in a number of types of cancer and may thus be potential targets in cancer therapy. Several Aurora kinase inhibitors have been identified and developed. Some of these have been used in clinical trials and have exhibited certain efficacy in cancer treatment. However, none of these has yet been applied clinically due to the poor outcomes. Oxostephanine is an aporphine alkaloid isolated from several plants of the genus Stephania. This compound has been reported to inhibit Aurora kinase activity in kinase assays and in cancer cells. The present study aimed to investigate the real‑time effects of oxostephanine extracted from

Indexed as

Antineoplastic AgentsEndothelial CellsHumansPhosphorylationProtein Kinase InhibitorsProtein Serine-Threonine KinasesAntineoplastic AgentsProtein Kinase InhibitorsProtein Serine-Threonine KinasesangiogenesisAurora kinase inhibitorAurora kinasesendothelial cellsgrowth factorsovary cancer cell line

Identifiers

PMID36102296
PMCPMC9558763
OpenAlexW4295366615

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.