Evidence map›Paper›PMID 33187536›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

Targeting HMGB3/hTERT axis for radioresistance in cervical cancer.

Zongjuan Li, Yang Zhang, Silei Sui, Yijun Hua, Anshi Zhao, Xiaoyuan Tian, Ruonan Wang, Wei Guo, Wendan Yu, Kun Zou and 3 more

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 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  10. Role of telomerase in the onset and treatment of gastric cancer.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Review
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  14. Structure and Functions of HMGB3 Protein.International journal of molecular sciences · 2024
    Review
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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

13 authors at 7 institutions in 1 country.

Zongjuan LiThe Second Affiliated Hospital & Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Yang ZhangQingdao University Medical College Affiliated Yantai Yuhuangding Hospital, Yantai, China.
Silei SuiThe Second Affiliated Hospital & Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Yijun HuaSunYat-sen University Cancer Center; State Key Laboratory of Oncology in South China; Collaborative Innovation Center of Cancer Medicine, Guangzhou, China.
Anshi ZhaoSunYat-sen University Cancer Center; State Key Laboratory of Oncology in South China; Collaborative Innovation Center of Cancer Medicine, Guangzhou, China.
Xiaoyuan TianThe Second Affiliated Hospital & Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Ruonan WangThe Second Affiliated Hospital & Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Wei GuoThe Second Affiliated Hospital & Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Wendan YuThe Second Affiliated Hospital & Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Kun ZouThe First Affiliated Hospital, Dalian Medical University, Dalian, China.
Wuguo DengSunYat-sen University Cancer Center; State Key Laboratory of Oncology in South China; Collaborative Innovation Center of Cancer Medicine, Guangzhou, China. dengwg@sysucc.org.cn.
Liru HeSunYat-sen University Cancer Center; State Key Laboratory of Oncology in South China; Collaborative Innovation Center of Cancer Medicine, Guangzhou, China. helr@sysucc.org.cn.
Lijuan ZouThe Second Affiliated Hospital & Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China. zoulijuan1963@sina.com.
Dalian Medical University · CNSecond Affiliated Hospital of Dalian Medical University · CNSun Yat-sen University Cancer Center · CNFirst Affiliated Hospital of Dalian Medical University · CNQingdao University · CNState Key Laboratory of Oncology in South ChinaSun Yat-sen University · CN

Funding

National Natural Science Foundation of China 81473452National Natural Science Foundation of China 81703904
6 · The paper itself

Abstract

backgroundRadiotherapy is regarded as a milestone for the cure of cervical cancer. However, clinical outcome heavily be hindered by radioresistance. So, exploring the underlying mechanism of radioresistance, and find potential target, well deserve fully emphasis.

methodsIn this study, we developed two novel radiation resistance cervical cancer cell lines, which could mimic clinical radioresistance. In order to find new potential targets, RNA-Seq, database analysis, streptavidin-agarose and LC/MS were used. Pull-down, luciferase and rescue assays were conducted to explore the regulatory mechanisms. To further evaluate the correlation between therapeutic responses and HMGB3/hTERT expression, 172 cervical cancer patients were recruited.

resultsKnockdown of HMGB3 significantly inhibit the DNA damage repair and induced more γH2AX foci, leading to enhanced chemo- and radio-sensitivity in vitro and in vivo, whereas HMGB3 overexpression has the opposite effects. HMGB3 promotes cell growth and radioresistance by transcriptionally up-regulating hTERT via the specifical binding of HMGB3 at the hTERT promoter region from - 902 to - 321. HMGB3 knockdown-mediated radiosensitization could be reversed by the overexpressed hTERT in both cervical cancer cell lines and xenograft tumor mouse model. Furthermore, clinical data from 172 cervical cancer patients proved that there was a positive correlation between HMGB3 and hTERT expression, and high expression of HMGB3/hTERT predicted poor response to radiotherapy, worse TNM stages and shorter survival time.

conclusionHere, we have identified HMGB3/hTERT signaling axis as a new target for cervical cancer radioresistance. Our results provide new insights into the mechanism of cervical cancer radioresistance and indicate that targeting the HMGB3/hTERT signaling axis may benefit cervical cancer patients.

Indexed as

AnimalsCell Line, TumorFemaleHMGB3 ProteinHumansMiceMice, NudeMiddle AgedRadiation ToleranceSignal TransductionTransfectionUterine Cervical NeoplasmsHMGB3 ProteinCervical cancerHMGB3hTERTRadioresistance

Identifiers

PMID33187536
PMCPMC7664109
OpenAlexW3101816108

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.