Evidence map›Paper›PMID 37728702›Full record

ArticleJournal of cancer research and clinical oncology2023

Downregulated BIRC5 inhibits proliferation and metastasis of melanoma through the β-catenin/HIF-1α/VEGF/MMPs pathway.

Qingqing He, Yijing He, Changqiang Li, Jianv Wang, Tong Xia, Xia Xiong, Jixiang Xu, Li Liu

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

8 authors at 2 institutions in 1 country.

Qingqing He *Department of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China.
Yijing He *Department of Science and Technology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China.
Changqiang LiDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China.
Jianv WangDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China.
Tong XiaDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China.
Xia XiongDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China.
Jixiang Xu *Department of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China. xujx888@163.com.
Li Liu *Department of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, China. liuli@swmu.edu.cn.ORCID http://orcid.org/0000-0003-3086-9981
Affiliated Hospital of Southwest Medical University · CNSouthwest Medical University · CN

Funding

Luzhou Science and Technology Projects 2022-JYJ-141Sichuan Science and Technology Program 2022YFS0631Southwest Medical University School-level Project Fund 2022QN044the National Natural Science Foundation of China 82003716
6 · The paper itself

Abstract

purposeMelanoma is a malignant skin tumor caused by melanocytes and associated with high mortality rates. This study aims to investigate the specific mechanism of ZWZ-3 in melanoma proliferation and metastasis.

methodsRNA sequencing was performed to identify the effect of ZWZ-3 on gene expression. siRNA was used to inhibit BIRC5 gene expression in the B16F10 cell line. A zebrafish tumor model was used to assess the therapeutic effect of ZWZ-3 in vivo. Mechanistic insights into the inhibition of tumor metastasis by ZWZ-3 were obtained through analysis of tumor tissue sections in mice.

resultsOur findings demonstrated that ZWZ-3 suppressed melanoma cell proliferation and migration. We performed RNA sequencing in melanoma cells after the treatment with ZWZ-3 and found that Birc5, which is closely associated with tumor metastasis, was significantly down-regulated. Bioinformatics analysis and the immuno-histochemical results of tissue chips for melanoma further confirmed the high expression of BIRC5 in melanoma and its effect on disease progression. Moreover, Birc5 knock-down significantly inhibited melanoma cell proliferation and metastasis, which was correlated with the β-catenin/HIF-1α/VEGF/MMPs pathway. Additionally, ZWZ-3 significantly inhibited tumor growth in the zebrafish tumor model without any evident side effects. Histological and immuno-histochemical analyses revealed that ZWZ-3 inhibited tumor cell metastasis by down-regulating HIF-1α, VEGF, and MMP9.

conclusionOur findings revealed that ZWZ-3 could downregulate BIRC5 and inhibit melanoma proliferation and metastasis through the β-catenin/HIF-1α/VEGF/MMPs pathway. Therefore, BIRC5 represents a promising therapeutic target for the treatment of melanoma.

Indexed as

MelanomaVascular Endothelial Growth Factor AAnimalsbeta CateninCell Line, TumorCell ProliferationHypoxia-Inducible Factor 1, alpha SubunitMiceZebrafishbeta CateninHypoxia-Inducible Factor 1, alpha SubunitVascular Endothelial Growth Factor ABIRC5MelanomaMetastasisProliferationβ-Catenin/HIF-1α/VEGF/MMPs

Identifiers

PMID37728702
PMCPMC11797675
OpenAlexW4386877728

What OpenQuestion holds

Textmetadata
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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.