Evidence map›Paper›PMID 40547154›Full record

ArticleWorld journal of gastrointestinal oncology2025

Oxocrebanine inhibits the proliferation of hepatocellular carcinoma cells by promoting apoptosis and autophagy.

Zheng-Wen Wang, Cai-Yan Pan, Cang-Long Wei, Hui Liao, Xiao-Po Zhang, Cai-Yun Zhang, Lei Yu

Abstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Zheng-Wen WangDepartment of Hepatobiliary and Pancreatic Surgery/Hainan Clinical Medical Research Center for Liver Disease and Liver Critical Illness, Hainan Cancer Hospital/Hainan Medical University Affiliated Cancer Hospital, Haikou 570312, Hainan Province, China.
Cai-Yan PanDepartment of Hepatobiliary and Pancreatic Surgery/Hainan Clinical Medical Research Center for Liver Disease and Liver Critical Illness, Hainan Cancer Hospital/Hainan Medical University Affiliated Cancer Hospital, Haikou 570312, Hainan Province, China.
Cang-Long WeiDepartment of Hepatobiliary and Pancreatic Surgery/Hainan Clinical Medical Research Center for Liver Disease and Liver Critical Illness, Hainan Cancer Hospital/Hainan Medical University Affiliated Cancer Hospital, Haikou 570312, Hainan Province, China.
Hui LiaoDepartment of Hepatobiliary and Pancreatic Surgery/Hainan Clinical Medical Research Center for Liver Disease and Liver Critical Illness, Hainan Cancer Hospital/Hainan Medical University Affiliated Cancer Hospital, Haikou 570312, Hainan Province, China.
Xiao-Po ZhangDepartment of Analysis, Hainan Pharmaceutical Research and Development Science and Technology Park, Haikou 570312, Hainan Province, China.
Cai-Yun ZhangDepartment of Analysis, Hainan Pharmaceutical Research and Development Science and Technology Park, Haikou 570312, Hainan Province, China. zhangcaiyunhaikou@163.com.
Lei YuCollege of Pharmacy/Drug Engineering Technology Research Center, Harbin University of Commerce, Harbin 150076, Heilongjiang Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFinding active lead anti-hepatocellular carcinoma compounds from traditional Chinese medicine has important research value.

aimTo assess the detailed mechanism of oxocrebanine, a compound separated from the traditional Chinese medicinal plant

methodsMTT, BrdU labeling, and colony formation assays were used to assess the inhibitory effect of oxocrebanine on the growth and proliferation of human hepatocellular carcinoma Hep3B2.1-7 cells. Flow cytometry was used to detect the effect of oxocrebanine on the apoptosis of Hep3B2.1-7 cells. Western blotting was used to assess the expression of apoptosis-related proteins in Hep3B2.1-7 cells. The aforementioned methods were also used to evaluate the effects of oxocrebanine on cell proliferation, autophagy markers, and autophagy-related protein expression levels after adding autophagy inhibitor 3-mA. Furthermore, to verify the anti-hepatocellular carcinoma effect of oxocrebanine

resultsOxocrebanine effectively inhibited the growth of Hep3B2.1-7 cells, whilst upregulating the protein expression of cleaved caspase-3, downregulating poly(ADP-ribose) polymerase 1 protein expression, increasing the levels of Bax and Bcl-2 antagonist/killer 1 protein expression, and decreasing the levels of Bcl-2 and myeloid cell leukemia 1 protein expression, which could promote apoptosis in Hep3B2.1-7 cells. Oxocrebanine promoted the transformation of LC3-I to LC3-II in Hep3B2.1-7 cells, suggesting the occurrence of autophagy, whilst the autophagy inhibitor 3-MA could reverse this process. Oxocrebanine was also shown to reduce the phosphorylation levels of the eukaryotic translation initiation factor 4EBP1 and ribosomal protein S6 kinase B1 (P70S6K), two downstream effector molecules in the PI3K/Akt/mTOR pathway, inducing autophagy in Hep3B2.1-7 cells. Moreover, the tumor-bearing nude mouse experiment indicated that oxocrebanine effectively inhibited the growth of Hep3B2.1-7 cells

conclusionOxocrebanine can inhibit the proliferation of human hepatocellular carcinoma cells by promoting apoptosis and inducing autophagy

Indexed as

ApoptosisAutophagyHep3B2.1-7 cellsOxocrebanineStephania hainanensis H.S. Lo et Y. Tsoong

Identifiers

PMID40547154
PMCPMC12179960

What Socratic holds

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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 Socratic graph.