Evidence map›Paper›PMID 36605485›Full record

ArticleJournal of Cancer2023

S100A11: A Potential Carcinogen and Prognostic Marker That Correlates with the Immunosuppressive Microenvironment in Pan-Cancer.

Xiaozhen Ji, Xin Qin, Xiuming Huang, Wei Wang, Huiyan Li, Chuizhi Zheng, Yanjing Huang

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 18 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

7 authors at 1 institution in 1 country.

Xiaozhen JiDepartment of Oncology, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) , Haikou 570311, Hainan, China.
Xin QinDepartment of Radiology, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) , Haikou 570311, Hainan, China.
Xiuming HuangDepartment of Thoracic Surgery, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) , Haikou 570311, Hainan, China.
Wei WangDepartment of Oncology, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) , Haikou 570311, Hainan, China.
Huiyan LiDepartment of Oncology, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) , Haikou 570311, Hainan, China.
Chuizhi ZhengDepartment of Oncology, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) , Haikou 570311, Hainan, China.
Yanjing HuangDepartment of Oncology, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) , Haikou 570311, Hainan, China.
Hainan General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

S100 calcium-binding protein A11 (S100A11) has been proved to be an oncogene of most tumors. However, its role in the tumor microenvironment (TME) in pan-cancer stills remains poorly understood. This study used public data from The Cancer Genome Atlas (TCGA) and the Genotype-Tissue Expression (GTEx) database to evaluate the expression of S100A11. The R package "GSVA" was used for Gene set variation analysis (GSVA) of S100A11. The R package "ESTIMATE" was used to further explore the relationship between S100A11 and TME. The Genomics of Drug Sensitivity in Cancer database was used to investigate the effect of S100A11 on the efficiency of anticancer drugs. We found S100A11 expression was upregulated in most tumors and predicted a poor prognosis. Furthermore, S100A11 expression was closely associated with immune regulation-related pathways. Moreover, S100A11 expression in pan-cancer was significantly related to most immunosuppressive cells, such as tumor-associated macrophages (TAM), tumor-associated fibroblasts (TAF), and Treg cells. The expression of S100A11 was significantly related to immunosuppressive genes and immune checkpoints in most tumor types. Additionally, the upregulation of S100A11 expression made patients with cancer resistant to the treatment of most anticancer drugs, such as sorafenib. In brief, our study showed that S100A11 could be used as a potential carcinogen and prognostic marker for most tumor types. The increased expression of S100A11 was closely related to tumor immunosuppressive TME. The upregulation of S100A11 expression made patients with cancer resistant to sorafenib treatment.

Indexed as

Drug resistantimmunosuppressiveS100A11TCGAtumor microenvironment

Identifiers

PMID36605485
PMCPMC9809332
OpenAlexW4313514449

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.