Evidence map›Paper›PMID 37684630›Full record

ArticleJournal of experimental & clinical cancer research : CR2023

SENP5 promotes homologous recombination-mediated DNA damage repair in colorectal cancer cells through H2AZ deSUMOylation.

Tingting Liu, Hang Wang, Yuanyuan Chen, Zhijie Wan, Zhipeng Du, Hui Shen, Yue Yu, Shengzhe Ma, Ying Xu, Zhuqing Li and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2023. 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
4.2field-weighted citation impact, top 5% 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, 27 citations in OpenAlex.

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  20. SUMO and the DNA damage response.Biochemical Society transactions · 2024
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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

17 authors at 2 institutions in 1 country.

Tingting Liu *Department of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Hang Wang *Department of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Yuanyuan Chen *Department of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Zhijie Wan *Department of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Zhipeng DuSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Hui ShenDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Yue YuDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Shengzhe MaDepartment of Colorectal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Ying XuDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Zhuqing LiDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Nanxi YuSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Fangxiao ZhangSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Kun CaoDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China.
Jianming CaiSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Wei ZhangDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China. weizhang2000cn@163.com.
Fu GaoDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China. gaofusmmu@163.com.
Yanyong YangDepartment of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China. yyyang2010@163.com.
Wenzhou Medical University · CNSecond Military Medical University · CN

Funding

National Natural Science Foundation of China 81972968National Natural Science Foundation of China 82103776National Natural Science Foundation of China 82173462National Natural Science Foundation of China 82203979National Natural Science Foundation of China 82273579Science and Technology Project of Jiaxing City 2020AY30010Shanghai Science and Technology Development Foundation 23QA1114600South Zhejiang Institute of Radiation Medicine and Nuclear Technology No.ZFY-2021-K-002three-year plan of shanghai municipal health commission No. 20214Y0012Three-Year Plan of Shanghai Municipal Health Commission GWV-10.2-YQ27Zhejiang Provincial Natural Science Foundation of China LQ23H220001
6 · The paper itself

Abstract

backgroundNeoadjuvant radiotherapy has been used as the standard treatment of colorectal cancer (CRC). However, radiotherapy resistance often results in treatment failure. To identify radioresistant genes will provide novel targets for combined treatments and prognostic markers.

methodsThrough high content screening and tissue array from CRC patients who are resistant or sensitive to radiotherapy, we identified a potent resistant gene SUMO specific peptidase 5 (SENP5). Then, the effect of SENP5 on radiosensitivity was investigated by CCK8, clone formation, comet assay, immunofluorescence and flow cytometric analysis of apoptosis and cell cycle to investigate the effect of SENP5 on radiosensitivity. SUMO-proteomic mass spectrometry combined with co-immunoprecipitation assay were used to identify the targets of SENP5. Patient-derived organoids (PDO) and xenograft (PDX) models were used to explore the possibility of clinical application.

resultsWe identified SENP5 as a potent radioresistant gene through high content screening and CRC patients tissue array analysis. Patients with high SENP5 expression showed increased resistance to radiotherapy. In vitro and in vivo experiments demonstrated that SENP5 knockdown significantly increased radiosensitivity in CRC cells. SENP5 was further demonstrated essential for efficient DNA damage repair in homologous recombination (HR) dependent manner. Through SUMO mass spectrometry analysis, we characterized H2AZ as a deSUMOylation substrate of SENP5, and depicted the SUMOylation balance of H2AZ in HR repair and cancer resistance. By using PDO and PDX models, we found targeting SENP5 significantly increased the therapeutic efficacy of radiotherapy.

conclusionOur findings revealed novel role of SENP5 in HR mediated DNA damage repair and cancer resistance, which could be applied as potent prognostic marker and intervention target for cancer radiotherapy.

Indexed as

Colorectal NeoplasmsProteomicsDNA DamageHomologous RecombinationHumansRecombinational DNA RepairCancer resistancedeSUMOylationDNA damage repairSENP5

Identifiers

PMID37684630
PMCPMC10486113
OpenAlexW4386546077

What OpenQuestion holds

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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.