Evidence map›Paper›PMID 32020217›Full record

ArticleOncology reports2020

Ginsenoside CK induces apoptosis and suppresses proliferation and invasion of human osteosarcoma cells through the PI3K/mTOR/p70S6K1 pathway.

Kang Chen, Jianbao Jiao, Jinwei Xue, Taoping Chen, Yu Hou, Yuantao Jiang, Ligang Qian, Yunfei Wang, Zheng Ma, Zhixing Liang and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  13. Ginsenoside Compound K Enhances Fracture HealingFrontiers in pharmacology · 2022
    Article
  14. Review
  15. Aging · 2021
    Article
  16. Review
  17. Article
  18. Review
  19. 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

12 authors at 1 institution in 1 country.

Kang ChenDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Jianbao JiaoDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Jinwei XueDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Taoping ChenDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Yu HouDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Yuantao JiangDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Ligang QianDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Yunfei WangDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Zheng MaDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Zhixing LiangDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Bo SunDepartment of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Qiao RenDepartment of Rheumatism and Immunology, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Affiliated Hospital of Hebei University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is one of the most malignant bone tumors, and its major threats are aggressive invasion and early tumor metastasis, which result in a poor prognosis and high mortality. Accumulating evidence indicates that ginsenoside compound K (CK) has a significant antitumor effect, particularly on the inhibition of proliferation and invasion of numerous human tumors. In the present study, it was revealed that CK inhibited the viability and proliferation of osteosarcoma cells. Moreover, it was demonstrated that CK induced apoptosis and inhibited the migration and invasion of osteosarcoma cells via apoptotic staining, Annexin V/PI staining, and Transwell invasion assays. Furthermore, at the molecular level, the present results confirmed that apoptosis and invasion‑related proteins were regulated by CK, which was possibly related to the blockade of the PI3K/mTOR/p70S6K1 signaling pathway. In summary, the present findings indicated that CK inhibited viability and proliferation, induced apoptosis, and inhibited the migration and invasion of osteosarcoma cells through the PI3K/mTOR/p70S6K1 signaling pathway.

Indexed as

ApoptosisCell Line, TumorCell MovementCell ProliferationCell SurvivalGinsenosidesHumansNeoplasm InvasivenessOsteosarcomaPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRibosomal Protein S6 Kinases, 70-kDaSignal TransductionTOR Serine-Threonine Kinasesginsenoside compound KGinsenosidesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktribosomal protein S6 kinase, 70kD, polypeptide 1Ribosomal Protein S6 Kinases, 70-kDaTOR Serine-Threonine Kinasesapoptosisginsenoside CKinvasionosteosarcomaproliferation

Identifiers

PMID32020217
PMCPMC7041301
OpenAlexW3000542381

What Socratic 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 Socratic graph.