Evidence map›Paper›PMID 39790225›Full record

ArticleJournal of cancer prevention2024

Therapeutic Potential of Hongjam in A Diethylnitrosamine and Thioacetamide-induced Hepatocellular Carcinoma Mouse Model.

Young-Min Han, Hye-Rin Ahn, Da-Young Lee, Moon-Young Song, Seung-Won Lee, You-Kyung Jang, Byeong Yeob Jeon, Eun-Hee Kim

Abstract read
In one paragraph

Article in Journal of cancer prevention, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Young-Min Han *College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Seongnam, Korea.ORCID https://orcid.org/0000-0003-4335-9737
Hye-Rin Ahn *College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Seongnam, Korea.ORCID https://orcid.org/0009-0000-0613-2328
Da-Young LeeCollege of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Seongnam, Korea.ORCID https://orcid.org/0000-0001-7655-6740
Moon-Young SongCollege of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Seongnam, Korea.ORCID https://orcid.org/0000-0001-9311-5146
Seung-Won LeeCollege of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Seongnam, Korea.ORCID https://orcid.org/0009-0007-8301-6639
You-Kyung JangQBM Co., Ltd., Seoul, Korea.ORCID https://orcid.org/0009-0002-4965-8615
Byeong Yeob JeonQBM Co., Ltd., Seoul, Korea.ORCID https://orcid.org/0009-0008-3342-7656
Eun-Hee KimCollege of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Seongnam, Korea.ORCID https://orcid.org/0000-0002-8523-0440

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common and lethal type of primary liver cancer, frequently arising from chronic liver injury and inflammation. Despite treatment advancements, HCC prognosis remains poor, emphasizing the need for effective preventive and therapeutic strategies. This study investigates the hepatoprotective and anti-tumor effects of Hongjam, a steamed freeze-dried silkworm powder, in a diethylnitrosamine (DEN) and thioacetamide (TAA)-induced HCC mouse model. Mice were administered DEN intraperitoneally for 8 weeks, followed by TAA in drinking water for 9 weeks, with Hongjam supplementation (0.01, 0.1, and 1 g/kg) provided daily through food. Hongjam markedly reduced the tumor incidence, the size, and the histological lesions compared to the DEN/TAA group. Serum biochemical analysis revealed reduction in liver damage markers, including alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, and total bilirubin, with a notable decrease in total bilirubin surpassing. Immunohistochemical and Western blot analyses demonstrated that Hongjam downregulated expression of proliferation markers, including Ki67, phosphorylation of protein kinase B, and proliferating cell nuclear antigen, while upregulating the pro-apoptotic protein Bcl-2-associated X protein, indicating its dual role in suppressing proliferation and promoting apoptosis. Furthermore, Hongjam inhibited angiogenesis by suppressing the expression of key markers, including interleukin 6, VEGF, hypoxia-inducible factor-1 subunit alpha, platelet-derived growth factor subunit beta, matrix metalloproteinase-2, and cluster of differentiation 31, thereby disrupting the tumor microenvironment. These findings suggest that Hongjam exerts multifaceted protective effects against HCC by targeting proliferation, apoptosis, and angiogenesis pathways, while also mitigating liver damage. This study highlights the potential of Hongjam as a functional food or a complementary therapeutic agent for HCC prevention and management.

Indexed as

AngiogenesisAnti-proliferationDiethylnitrosamineHepatocellular carcinomaHongjamThioacetamide

Identifiers

PMID39790225
PMCPMC11706731

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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.