Evidence map›Paper›PMID 32862187›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2020

Asiaticoside Antagonizes Proliferation and Chemotherapeutic Drug Resistance in Hepatocellular Carcinoma (HCC) Cells.

Ying Ma, Jun Wen, Jing Wang, Chunyan Wang, Yan Zhang, Lili Zhao, Jia Li, Xue Feng

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2020. 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
4.0field-weighted citation impact, top 7% 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, 27 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Ying MaSecond Department of Hepatopathy, Tianjin Second People's Hospital, Tianjin, China (mainland).
Jun WenSecond Department of Hepatopathy, Tianjin Second People's Hospital, Tianjin, China (mainland).
Jing WangSecond Department of Hepatopathy, Tianjin Second People's Hospital, Tianjin, China (mainland).
Chunyan WangSecond Department of Hepatopathy, Tianjin Second People's Hospital, Tianjin, China (mainland).
Yan ZhangSecond Department of Hepatopathy, Tianjin Second People's Hospital, Tianjin, China (mainland).
Lili ZhaoSecond Department of Hepatopathy, Tianjin Second People's Hospital, Tianjin, China (mainland).
Jia LiSecond Department of Hepatopathy, Tianjin Second People's Hospital, Tianjin, China (mainland).
Xue FengSecond Department of Hepatopathy, Tianjin Second People's Hospital, Tianjin, China (mainland).
Second Hospital of Tianjin Medical University · CNTianjin Medical University · CNXian Yang Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Hepatocellular carcinoma (HCC) is the fifth most prevalent malignant tumor in China after lung cancer, gastric cancer, esophageal cancer, and breast cancer, and has a high mortality rate. Though there are a series of therapeutic strategies is now available for HCC in clinical practice, the 5-year survival rate after surgery is still low. In addition, multi-drug resistance (MDR) is one of the most important factors responsible for the low survival rate and poor therapy response in HCC. Hence, novel treatment strategies and molecules for HCC need to be developed. MATERIAL AND METHODS We assessed the effect of asiaticoside, a natural product derived from Centella asiatica (L.) Urban, on HCC cell proliferation and drug resistance. RESULTS Our data indicated that asiaticoside significantly inhibited the proliferation of HCC cell lines QGY-7703 and Bel-7402 in a dose- and time-dependent manner. Moreover, asiaticoside significantly induced apoptosis in QGY-7703 and Bel-7402 cells. Treatment with asiaticoside also caused G1 cell cycle arrest in QGY-7703 and Bel-7402 cells. Western blot assay results indicated that the mechanism underlying the effects of asiaticoside involves inhibiting the activity of the PI3K/Akt and MAPK/ERK pathways. Furthermore, asiaticoside significantly antagonized P-gp-mediated MDR in HCC cells. CONCLUSIONS Our results suggest that asiaticoside has the potential to be applied in the treatment of HCC patients, but further evidence is needed to confirm our results, particularly in vivo efficacy.

Indexed as

Carcinoma, HepatocellularCell Line, TumorCell ProliferationDrug Resistance, NeoplasmHumansLiver NeoplasmsMAP Kinase Signaling SystemPhosphatidylinositol 3-KinasesTriterpenesasiaticosidePhosphatidylinositol 3-KinasesTriterpenes

Identifiers

PMID32862187
PMCPMC7480090
OpenAlexW3082505825

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.