Evidence map›Paper›PMID 36920183›Full record

ArticleAging2023

Characterization of SHCBP1 to prognosis and immunological landscape in pan-cancer: novel insights to biomarker and therapeutic targets.

Fei Jiang, Yanlong Shi, Yue Wang, Chang Ge, Jun Zhu, Hanlu Fang, Yu Zhang, Yixiao Zhang, Haokun Jian, Tong Lei and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Ginsenoside Rh7 affects β-catenin nuclear translocation by inhibitingInternational journal of medical sciences · 2025
    Article
  5. 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

14 authors at 9 institutions in 1 country.

Fei JiangDepartment of General Surgery, Fuyang Hospital of Anhui Medical University, Fuyang, Anhui, China.
Yanlong ShiHepatopancreatobiliary Center, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Yue WangDepartment of Pathology, Anhui Medical University, Hefei, Anhui, China.
Chang GeDepartment of General Surgery, Fuyang Hospital of Anhui Medical University, Fuyang, Anhui, China.
Jun ZhuDepartment of Oncology, Fuyang Hospital of Anhui Medical University, Fuyang, Anhui, China.
Hanlu FangSchool of Basic Medicine, Hebei Medical University, Shijiazhuang, Hebei, China.
Yu ZhangThe Second Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Yixiao ZhangThe First Clinical College of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Haokun JianSchool of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.
Tong LeiThe First Affiliated Hospital, Nanchang University, Nanchang, Jiangxi, China.
Sheng LanThe Second Clinical College Clinical Medicine, Guangzhou Medical University, Guangzhou, Guangdong, China.
Liyu CaoDepartment of Pathology, Anhui Medical University, Hefei, Anhui, China.
Hongzhu YuDepartment of General Surgery, Fuyang Hospital of Anhui Medical University, Fuyang, Anhui, China.
Debao FangSchool of Basic Medical Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Anhui Medical University · CNFirst Affiliated Hospital of Nanchang University · CNGuangzhou Medical University · CNHebei Medical University · CNLanzhou University · CNSecond Affiliated Hospital of Nanjing Medical University · CNUniversity of Science and Technology of China · CNXinxiang Medical University · CNZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies have revealed the significant roles of SHC SH2 domain-binding protein 1 (SHCBP1) in occurrence and progression of cancers, but there is no pan-cancer analysis of SHCBP1.

methodsIn this study, we explored the potential carcinogenic role of SHCBP1 across 33 tumors from the TCGA and GTEx databases. We investigated SHCBP1 expression, prognosis, genetic alterations, tumor mutational burden (TMB) score, microsatellite instability (MSI) and tumor microenvironment from TIMER2, GEPIA2, UALCAN and cBioPortal databases. Moreover, the cellular functions and potential mechanisms were evaluated by GO and KEGG analysis. Besides, the mRNA expression of SHCBP1 was examined using qRT-PCR assay in gastrointestinal cancers.

resultsSHCBP1 was significantly upregulated in various cancers, and apparent relationship existed between SHCBP1 and survival prognosis in patients. The TMB, MSI, and tumor microenvironment analysis indicated that SHCBP1 was closely related to immune checkpoints, immune targets, as well as CD4+ naive T cell, CD8+ T cell, and neutrophil. Moreover, the cellular functions of SHCBP1 were mainly in regulating cell cycle motor protein activity. In addition, we validated that SHCBP1 mRNA expression was over-expressed in gastrointestinal cancers.

conclusionsThis study was the first to systematically determine the prognostic value of SHCBP1, providing a forward-looking perspective on immunotherapy and cellular processes in pan-cancer.

Indexed as

NeoplasmsBiomarkersCell Cycle ProteinsHumansImmunotherapyMicrosatellite InstabilityPrognosisRNA, MessengerShc Signaling Adaptor ProteinsTumor MicroenvironmentBiomarkersCell Cycle ProteinsRNA, MessengerSHCBP1 protein, humanShc Signaling Adaptor Proteinsbiomarkerimmune microenvironmentpan-cancerprognosisSHCBP1

Identifiers

PMID36920183
PMCPMC10085602
OpenAlexW4324138127

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.