Evidence map›Paper›PMID 36359790›Full record

ArticleCells2022

Whole Transcriptome Sequencing Reveals Cancer-Related, Prognostically Significant Transcripts and Tumor-Infiltrating Immunocytes in Mantle Cell Lymphoma.

Esra Esmeray Sönmez, Tevfik Hatipoğlu, Deniz Kurşun, Xiaozhou Hu, Burcu Akman, Hongling Yuan, Ayça Erşen Danyeli, İnci Alacacıoğlu, Sermin Özkal, Aybüke Olgun and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Review
  5. Article
  6. Journal of clinical medicine · 2025
    Article
  7. Article
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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

13 authors at 3 institutions in 2 countries.

Esra Esmeray Sönmezİzmir International Biomedicine and Genome Institute, Dokuz Eylül University, İzmir 35340, Türkiye.
Tevfik Hatipoğluİzmir International Biomedicine and Genome Institute, Dokuz Eylül University, İzmir 35340, Türkiye.
Deniz Kurşunİzmir International Biomedicine and Genome Institute, Dokuz Eylül University, İzmir 35340, Türkiye.
Xiaozhou Huİzmir International Biomedicine and Genome Institute, Dokuz Eylül University, İzmir 35340, Türkiye.
Burcu Akmanİzmir International Biomedicine and Genome Institute, Dokuz Eylül University, İzmir 35340, Türkiye.ORCID 0000-0002-1929-5836
Hongling Yuanİzmir International Biomedicine and Genome Institute, Dokuz Eylül University, İzmir 35340, Türkiye.ORCID 0000-0002-4858-2471
Ayça Erşen DanyeliDepartment of Pathology, Faculty of Medicine, Dokuz Eylül University, İzmir 35340, Türkiye.
İnci AlacacıoğluDepartment of Hematology, Faculty of Medicine, Dokuz Eylül University, İzmir 35340, Türkiye.
Sermin ÖzkalDepartment of Pathology, Faculty of Medicine, Dokuz Eylül University, İzmir 35340, Türkiye.
Aybüke OlgunDepartment of Hematology, Faculty of Medicine, Dokuz Eylül University, İzmir 35340, Türkiye.
Taner Kemal ErdağDepartment of Otorhinolaryngology, Faculty of Medicine, Dokuz Eylül University, İzmir 35340, Türkiye.
Hua YouChongqing Key Laboratory of Pediatrics, Ministry of Education Key Laboratory of Child Development and Disorders, Department of Hematology and Oncology, Children's Hospital of Chongqing Medical University, Chongqing 401122, China.ORCID 0000-0002-9630-5284
Can Küçükİzmir International Biomedicine and Genome Institute, Dokuz Eylül University, İzmir 35340, Türkiye.ORCID 0000-0001-5540-9012
Dokuz Eylül University · TRIzmir University · TRChildren's Hospital of Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mantle cell lymphoma (MCL) is an aggressive B-cell non-Hodgkin lymphoma (NHL) subtype characterized by overexpression of CCND1 and SOX11 genes. It is generally associated with clinically poor outcomes despite recent improvements in therapeutic approaches. The genes associated with the development and prognosis of MCL are still largely unknown. Through whole transcriptome sequencing (WTS), we identified mRNAs, lncRNAs, and alternative transcripts differentially expressed in MCL cases compared with reactive tonsil B-cell subsets. CCND1, VCAM1, and VWF mRNAs, as well as MIR100HG and ROR1-AS1 lncRNAs, were among the top 10 most significantly overexpressed, oncogenesis-related transcripts. Survival analyses with each of the top upregulated transcripts showed that MCL cases with high expression of VWF mRNA and low expression of FTX lncRNA were associated with poor overall survival. Similarly, high expression of MSTRG.153013.3, an overexpressed alternative transcript, was associated with shortened MCL survival. Known tumor suppressor candidates (e.g., PI3KIP1, UBXN) were significantly downregulated in MCL cases. Top differentially expressed protein-coding genes were enriched in signaling pathways related to invasion and metastasis. Survival analyses based on the abundance of tumor-infiltrating immunocytes estimated with CIBERSORTx showed that high ratios of CD8

Indexed as

Lymphocytes, Tumor-InfiltratingLymphoma, Mantle-CellRNA, Long NoncodingAdultBiomarkers, TumorCarcinogenesisCD8-Positive T-LymphocytesExome SequencingHumansPrognosisRNA, Messengervon Willebrand FactorBiomarkers, TumorRNA, Long NoncodingRNA, Messengervon Willebrand Factoralternative transcriptlncRNAmantle cell lymphomamRNAoncogeneprognosistumor microenvironmenttumor suppressorWTS

Identifiers

PMID36359790
PMCPMC9654955
OpenAlexW4307635375

What OpenQuestion 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 OpenQuestion graph.