Evidence map›Paper›PMID 35452413›Full record

ArticleAging2022

Integrated analysis of 14 lymphoma datasets revealed high expression of CXCL14 promotes cell migration in mantle cell lymphoma.

Dahai Liu, Fei Qi, Wei Liu, Justin Liu, Jun Wang, Dao-Qiang Lu, Yang Xun, Min-Min Chen, Xin Chen, Shu-Ting Yang and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

15 authors at 5 institutions in 2 countries.

Dahai LiuFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Fei QiDepartment of Respiratory and Critical Care Medicine, Peking University Shenzhen Hospital, Futian District, Shenzhen 518036, Guangdong, China.
Wei LiuDepartment of Pharmacy, Anhui Medical College, Hefei 230601, Anhui, China.
Justin LiuDepartment of Statistics, University of California, Riverside, CA 92521, USA.
Jun WangFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Dao-Qiang LuSchool of Life Science and Engineering, Foshan University, Foshan 528000, Guangdong, China.
Yang XunFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Min-Min ChenFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Xin ChenFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Shu-Ting YangFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Wen-Qiao JiaoFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Zong-Ye LiFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Fang LiuFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Hua YangFoshan Stomatology Hospital and School of Medicine, Foshan University, Foshan 528000, Guangdong, China.
Wen-Xing LiDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, Guangdong, China.
Foshan University · CNStomatology Hospital · CNAnhui Medical University · CNPeking University Shenzhen Hospital · CNUniversity of California, Riverside · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphoma is accompanied by the impairment of multiple immune functions. Cytokines play an important role in a variety of immune-related functions and affect the tumor microenvironment. However, the exact regulatory mechanisms between them remain unclear. This study aimed to explore the cytokines expression and function in Hodgkin's lymphoma (HL), diffuse large B-cell lymphoma (DLBCL), and mantle cell lymphoma (MCL). We performed a transcriptome integration analysis of 14 lymphoma datasets including 240 Hodgkin's lymphoma, 891 diffuse large B-cell lymphoma, 216 mantle cell lymphoma, and 64 health samples. The results showed that multiple immune functions and signal pathway damage were shared by all three types of lymphoma, and these functions were related to cytokines. Furthermore, through co-expression network and functional interaction network analysis, we identified CXCL14 as a key regulator and it affects cell chemotaxis and migration functions. The functional experiment showed that CXCL14 knockdown inhibited cell migration in MCL cell lines. This study suggested that high expression of CXCL14 may aggravate MCL via promoting cell migration. Our findings provide novel insights into the biology of this disease and would be helpful for the pathogenesis study and drug discovery of lymphomas.

Indexed as

Hodgkin DiseaseLymphoma, Large B-Cell, DiffuseLymphoma, Mantle-CellCell MovementChemokines, CXCCytokinesHumansTumor MicroenvironmentChemokines, CXCCXCL14 protein, humanCytokinescell migrationCXCL14cytokinesgene expressionmantle cell lymphoma

Identifiers

PMID35452413
PMCPMC9085238
OpenAlexW4225463409

What Socratic holds

Textmetadata
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 Socratic graph.