Evidence map›Paper›PMID 32410646›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

Promotion of ubiquitination-dependent survivin destruction contributes to xanthohumol-mediated tumor suppression and overcomes radioresistance in human oral squamous cell carcinoma.

Ming Li, Feng Gao, Xinfang Yu, Qing Zhao, Li Zhou, Wenbin Liu, Wei Li

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

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  7. In Silico Molecular Docking ofJournal of pharmacy & bioallied sciences · 2024
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  12. Survivin degradation by bergenin overcomes pemetrexed resistance.Cellular oncology (Dordrecht, Netherlands) · 2023
    Article
  13. Article
  14. Review
  15. Anticancer Potential of Natural Chalcones: In Vitro and In Vivo Evidence.International journal of molecular sciences · 2023
    Review
  16. Article
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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

7 authors at 3 institutions in 1 country.

Ming LiCell Transplantation and Gene Therapy Institute, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, People's Republic of China.
Feng GaoCell Transplantation and Gene Therapy Institute, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, People's Republic of China.
Xinfang YuCell Transplantation and Gene Therapy Institute, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, People's Republic of China.
Qing ZhaoChangsha Stomatological Hospital, Changsha, Hunan, 410004, People's Republic of China.
Li ZhouDepartment of Pathology, Xiangya Hospital of Central South University, Changsha, Hunan, 410008, People's Republic of China.
Wenbin LiuDepartment of Pathology, Hunan Cancer Hospital, Changsha, Hunan, 410013, People's Republic of China.
Wei LiCell Transplantation and Gene Therapy Institute, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, People's Republic of China. weililx@csu.edu.cn.ORCID http://orcid.org/0000-0002-7267-6494
Central South University · CNHunan Cancer Hospital · CNHunan University of Traditional Chinese Medicine · CN

Funding

National Natural Science Foundation of China 81904262National Natural Science Foundation of China 81972837Natural Science Foundation of Hunan Province 2018JJ2604Natural Science Foundation of Hunan Province 2018JJ3787Natural Science Foundation of Hunan Province 2019JJ50682
6 · The paper itself

Abstract

backgroundOverexpression of survivin plays a crucial role in tumorigenesis and correlates with poor prognosis in human malignancies. Thus, survivin has been proposed as an attractive target for new anti-tumor interventions.

methodsA natural product library was used for natural compound screening through MTS assay. The expression of survivin in oral squamous cell carcinoma (OSCC) and the inhibitory effect of xanthohumol (XN) on OSCC were examined by anchorage-dependent and -independent growth assays, immunoblot, immunofluorescence, immunohistochemical staining, ubiquitination analysis, co-immunoprecipitation assay, CRISPR-Cas9-based gene knockout, and xenograft experiment.

resultsSurvivin is highly expressed in OSCC patient-derived tissues and cell lines. Knockout of survivin reduced the tumorigenic properties of OSCC cells in vitro and in vivo. With a natural compound screening, we identified that xanthohumol inhibited OSCC cells by reducing survivin protein level and activating mitochondrial apoptotic signaling. Xanthohumol inhibited the Akt-Wee1-CDK1 signaling, which in turn decreased survivin phosphorylation on Thr34, and facilitated E3 ligase Fbxl7-mediated survivin ubiquitination and degradation. Xanthohumol alone or in combination with radiation overcame radioresistance in OSCC xenograft tumors.

conclusionOur findings indicate that targeting survivin for degradation might a promising strategy for OSCC treatment.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationDisease Models, AnimalFlavonoidsHumansMiceMouth NeoplasmsPropiophenonesRadiation ToleranceRandom AllocationSignal TransductionSquamous Cell Carcinoma of Head and NeckSurvivinUbiquitinationAntineoplastic AgentsBIRC5 protein, humanFlavonoidsPropiophenonesSurvivinxanthohumolFbxl7Oral squamous cell carcinomaUbiquitinationXanthohumol

Identifiers

PMID32410646
PMCPMC7227341
OpenAlexW3024816859

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.