Evidence map›Paper›PMID 38773427›Full record

ArticleBMC cancer2024

Effect of novel anti-tumor and anti-angiogenesis drug taurolactone on angiogenic factor AGGF1 and angiogenesis mimicry in patients with hepatocellular carcinoma.

Shaoping Liu, Yinzhi Wei, Lei Nie, Ze Tang, Qi Lu, Qun Liang

Abstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Shaoping LiuDepartment of General Practice, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, No.43 Wuhan Road, Huangshigang District, Huangshi, 435000, Hubei, China.
Yinzhi WeiDepartment of General Practice, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, No.43 Wuhan Road, Huangshigang District, Huangshi, 435000, Hubei, China.
Lei NieDepartment of Abdominal Tumor Surgery, Hubei Province Cancer Hospital, Wuhan, China.
Ze TangDepartment of Abdominal Oncology, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi, China.
Qi LuDepartment of HepatobiliarySurgery, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi, China.
Qun LiangDepartment of General Practice, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, No.43 Wuhan Road, Huangshigang District, Huangshi, 435000, Hubei, China. 3344871925@qq.com.

Funding

Hubei Provincial Natural Science Foundation Innovation and Development Joint Fund No.2022CFD067
6 · The paper itself

Abstract

objectiveOur study was to investigate the impact of taurolactone, a novel anti-tumor and anti-angiogenic drug, on AGGF1, an angiogenic factor, and angiogenesis mimicry in patients diagnosed with hepatocellular carcinoma (HCC).

methodsA total of 120 HCC patients were enrolled from the Department of Oncology and Hepatobiliary Surgery at our hospital between May 2021 and December 2022. HCC diagnoses were confirmed through imaging or tissue biopsy for all patients. The age of patients ranged from 37 to 72 years, with an average age of 64.29 ± 4.58 years. These participants were divided equally into two groups: the control group and the observation group, each consisting of 60 individuals. While the control group received standard drug treatment, the observation group was administered taurolactone treatment. Before being included in the study, all participants or their legal representatives provided signed informed consent. Patient demographic information was collected through a questionnaire survey. ELISA was used to measure the levels of VEGF and AGGF1 in patients following treatment. Western blot was applied to assess the protein expression of PDGF, Angiopoietin, and AGGF1. MRI imaging technology was utilized to assess the perfusion characteristics of tumor blood vessels in patients. Tumor vessel density was compared between patients using ultrasonography. We also conducted a comparison between the two groups in terms of progression-free survival and overall survival.

resultsGeneral patient information between the two groups showed no significant differences (P > 0.05). Of note, the observation group exhibited greatly lower levels of VEGF and AGGF1 compared to the control group (P < 0.05). Moreover, the levels of PDGF, Angiopoietin, and AGGF1 protein expression were significantly reduced in the observation group compared to the control group (P < 0.05). In terms of tumor perfusion, the observation group displayed lower average and maximum perfusion volumes in tumor blood vessels compared to the control group (P < 0.05). Additionally, the observation group demonstrated delayed peak times and arrival times of tumor blood vessels in comparison to the control group (P < 0.05). Furthermore, the density of tumor blood vessels was notably lower in the observation group compared to the control group (P < 0.05). Patients in the observation group had longer progression-free survival and overall survival than the control group (P < 0.05).

conclusionIn HCC patients, our study highlighted the potential efficacy of taurolactone treatment as it effectively inhibited angiogenic factors and angiogenesis mimicry, ultimately leading to an improved prognosis for these patients.

Indexed as

Angiogenesis InhibitorsAngiogenic ProteinsCarcinoma, HepatocellularLiver NeoplasmsNeovascularization, PathologicAdultAgedAngiogenesisAntineoplastic AgentsFemaleHumansLactonesMaleMiddle AgedVascular Endothelial Growth Factor AAGGF1 protein, humanAngiogenesis InhibitorsAngiogenic ProteinsAntineoplastic AgentsLactonesVascular Endothelial Growth Factor AAngiogenesis mimicryAngiogenic factor AGGF1Hepatocellular carcinomaTaurolactone

Identifiers

PMID38773427
PMCPMC11106933

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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.