Evidence map›Paper›PMID 37268895›Full record

ArticleBiological procedures online2023

A multi-omics analysis reveals CLSPN is associated with prognosis, immune microenvironment and drug resistance in cancers.

Yihong Chen, Haicheng Wen, Yin Li, Ying Han, Jun Tan, Cao Guo, Changjing Cai, Ping Liu, Yinghui Peng, Yihan Liu and 4 more

Open access · goldAbstract read
In one paragraph

Article in Biological procedures online, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

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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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

14 authors at 2 institutions in 1 country.

Yihong ChenDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Haicheng WenDepartment of Spine Surgery and Orthopaedics, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Yin LiDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Ying HanDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Jun TanDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Cao GuoDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Changjing CaiDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Ping LiuDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Yinghui PengDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Yihan LiuDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Xinwen WangDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Shan ZengDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Ziyang FengDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. 2204140320@csu.edu.cn.
Hong ShenDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. hongshen2000@csu.edu.cn.
Xiangya Hospital Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmunotherapy is effective only in limited patients. It is urgent to discover a novel biomarker to predict immune cells infiltration status and immunotherapy response of different cancers. CLSPN has been reported to play a pivotal role in various biological processes. However, a comprehensive analysis of CLSPN in cancers has not been conducted.

methodsTo show the whole picture of CLSPN in cancers, a pan-cancer analysis was conducted in 9125 tumor samples across 33 cancer types by integrating transcriptomic, epigenomic and pharmacogenomics data. Moreover, the role of CLSPN in cancer was validated by CCK-8, EDU, colony formation and flow cytometry in vitro and tumor cell derived xenograft model in vivo.

resultsCLSPN expression was generally upregulated in most cancer types and was significantly associated with prognosis in different tumor samples. Moreover, elevated CLSPN expression was closely correlated with immune cells infiltration, TMB (tumor mutational burden), MSI (microsatellite instability), MMR (mismatch repair), DNA methylation and stemness score across 33 cancer types. Enrichment analysis of functional genes revealed that CLSPN participated in the regulation of numerous signaling pathways involved in cell cycle and inflammatory response. The expression of CLSPN in LUAD patients were further analyzed at the single-cell level. Knockdown CLSPN significantly inhibited cancer cell proliferation and cell cycle related cyclin-dependent kinase (CDK) family and Cyclin family expression in LUAD (lung adenocarcinoma) both in vitro and in vivo experiments. Finally, we conducted structure-based virtual screening by modelling the structure of CHK1 kinase domain and Claspin phosphopeptide complex. The top five hit compounds were screened and validated by molecular docking and Connectivity Map (CMap) analysis.

conclusionOur multi-omics analysis offers a systematic understanding of the roles of CLSPN in pan-cancer and provides a potential target for future cancer treatment.

Indexed as

CLSPNImmune infiltrationMulti-omicsPan-cancerPrognosisVirtual screening

Identifiers

PMID37268895
PMCPMC10239117
OpenAlexW4379184682

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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.