Evidence map›Paper›PMID 33455945›Full record

ArticleBiomolecules & therapeutics2021

SP-8356, a (1S)-(-)-Verbenone Derivative, Inhibits the Growth and Motility of Liver Cancer Cells by Regulating NF-κB and ERK Signaling.

Dong Hwi Kim, Hyo Jeong Yong, Sunam Mander, Huong Thi Nguyen, Lan Phuong Nguyen, Hee-Kyung Park, Hyo Kyeong Cha, Won-Ki Kim, Jong-Ik Hwang

Open access · hybridAbstract read
In one paragraph

Article in Biomolecules & therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 10 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

9 authors at 1 institution in 1 country.

Dong Hwi KimDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Hyo Jeong YongDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Sunam ManderDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Huong Thi NguyenDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Lan Phuong NguyenDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Hee-Kyung ParkDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Hyo Kyeong ChaDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Won-Ki KimDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Jong-Ik HwangDepartment of Biomedical Science, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Korea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver cancer is a common tumor and currently the second leading cause of cancer-related mortality globally. Liver cancer is highly related to inflammation as more than 90% of liver cancer arises in the context of hepatic inflammation, such as hepatitis B virus and hepatitis C virus infection. Despite significant improvements in the therapeutic modalities for liver cancer, patient prognosis is not satisfactory due to the limited efficacy of current drug therapies in anti-metastatic activity. Therefore, developing new effective anti-cancer agents with anti-metastatic activity is important for the treatment of liver cancer. In this study, SP-8356, a verbenone derivative with anti-inflammatory activity, was investigated for its effect on the growth and migration of liver cancer cells. Our findings demonstrated that SP-8356 inhibits the proliferation of liver cancer cells by inducing apoptosis and suppressing the mobility and invasion ability of liver cancer cells. Functional studies revealed that SP-8356 inhibits the mitogen-activated protein kinase and nuclear factor-kappa B signaling pathways, which are related to cell proliferation and metastasis, resulting in the downregulation of metastasis-related genes. Moreover, using an orthotopic liver cancer model, tumor growth was significantly decreased following treatment with SP-8356. Thus, this study suggests that SP-8356 may be a potential agent for the treatment of liver cancer with multimodal regulation.

Indexed as

ERKLiver cancerMotilityNF-κBProliferationSP-8356

Identifiers

PMID33455945
PMCPMC8094067
OpenAlexW3125578060

What OpenQuestion holds

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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.