Evidence map›Paper›PMID 35677365›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2022

Myricetin Induces Apoptosis and Protective Autophagy through Endoplasmic Reticulum Stress in Hepatocellular Carcinoma.

Anlai Ji, Lili Hu, Ding Ma, Guanghui Qiang, Dongliang Yan, Guang Zhang, Chunping Jiang

Open access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 17 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

7 authors at 1 institution in 1 country.

Anlai JiDepartment of Hepatobiliary Surgery, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.ORCID https://orcid.org/0000-0002-3680-003X
Lili HuDepartment of Hepatobiliary Surgery, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.ORCID https://orcid.org/0000-0001-8370-3331
Ding MaDepartment of Hepatobiliary Surgery, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.ORCID https://orcid.org/0000-0002-4778-7854
Guanghui QiangDepartment of Hepatobiliary Surgery, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.ORCID https://orcid.org/0000-0002-6360-3883
Dongliang YanDepartment of Hepatobiliary Surgery, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.ORCID https://orcid.org/0000-0002-0817-2347
Guang ZhangDepartment of Hepatobiliary Surgery, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.ORCID https://orcid.org/0000-0002-8392-9899
Chunping JiangDepartment of Hepatobiliary Surgery, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.ORCID https://orcid.org/0000-0002-5204-2531
Nanjing Drum Tower Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myricetin, a natural flavonoid, exhibits diverse biological activities, including antitumor effects. The present study aimed to investigate the effects of myricetin on hepatocellular carcinoma (HCC) cells and explore the underlying molecular mechanisms. Our results showed that myricetin significantly inhibited cell proliferation and induced apoptosis in HCC cells. The apoptosis induced by myricetin was associated with the activation of endoplasmic reticulum (ER) stress. In addition, autophagy was enhanced in response to ER stress. Inhibition of autophagy by RNA interference or chemical inhibitors resulted in increased apoptosis in myricetin-treated HCC cells. The in vivo experiment also showed that myricetin effectively reduced tumor growth in an HCC xenograft model and that combination treatment with an autophagy inhibitor significantly enhanced this effect. These results indicated that myricetin induced apoptosis in HCC cells through the activation of ER stress. Protective autophagy was also upregulated during this process. Simultaneous inhibition of autophagy enhanced the anti-HCC activity of myricetin. Myricetin might be a promising drug candidate for HCC therapy, and the combined use of myricetin with autophagy inhibitors could be an effective therapeutic strategy.

Identifiers

PMID35677365
PMCPMC9168098
OpenAlexW4282002400

What OpenQuestion holds

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Registered trials

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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.