Evidence map›Paper›PMID 34439306›Full record

ArticleCancers2021

Pan-Cancer Analysis of Prognostic and Immune Infiltrates for CXCs.

Long Li, Wenchao Yao, Sen Yan, Xianghui Dong, Zhenyi Lv, Qingxu Jing, Qiang Wang, Biao Ma, Chenjun Hao, Dongbo Xue and 1 more

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Pan-Cancer Analysis of the Prognostic and Immunological Role of SEMA7A.International journal of general medicine · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. 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

11 authors.

Long LiDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Wenchao YaoDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Sen YanKey Laboratory of Cardiac Diseases and Heart Failure, Harbin Medical University, Harbin 150001, China.
Xianghui DongKey Laboratory of Pathology, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Zhenyi LvDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Qingxu JingDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Qiang WangDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Biao MaDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Chenjun HaoDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Dongbo XueDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Dawei WangDepartment of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.

Funding

National Natural Science Foundation of China 81770634
6 · The paper itself

Abstract

backgroundCXCs are important genes that regulate inflammation and tumor metastasis. However, the expression level, prognosis value, and immune infiltration of CXCs in cancers are not clear.

methodsMultiple online datasets were used to analyze the expression, prognosis, and immune regulation of CXCs in this study. Network analysis of the Amadis database and GEO dataset was used to analyze the regulation of intestinal flora on the expression of CXCs. A mouse model was used to verify the fact that intestinal bacterial dysregulation can affect the expression of CXCs.

resultsIn the three cancers, multiple datasets verified the fact that the mRNA expression of this family was significantly different; the mRNA levels of CXCL3, 8, 9, 10, 14, and 17 were significantly correlated with the prognosis of three cancers. CXCs were correlated with six types of immuno-infiltrating cells in three cancers. Immunohistochemistry of clinical samples confirmed that the expression of CXCL8 and 10 was higher in three cancer tissues. Animal experiments have shown that intestinal flora dysregulation can affect CXCL8 and 10 expressions.

conclusionOur results further elucidate the function of CXCs in cancers and provide new insights into the prognosis and immune infiltration of breast, colon, and pancreatic cancers, and they suggest that intestinal flora may influence disease progression through CXCs.

Indexed as

genetic alterationimmune infiltrationmultiple tumorprognosissingle-cell sequencing

Identifiers

PMID34439306
PMCPMC8392715

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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.