Evidence map›Paper›PMID 40876452›Full record

ArticleCell reports. Medicine2025

Tumor evolution and immune microenvironment dynamics in primary and relapsed mantle cell lymphoma.

Hui Wan, Weicheng Ren, Mingyu Yang, Man Nie, Agata M Wasik, Likun Du, Leire de Campos-Mata, Rui Sun, Zhiliang Bai, Archibald Enninful and 14 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2025. 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
–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

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.

  1. [Advances in single cell omics applications in mantle cell lymphoma].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2026
    Review
  2. Advances in targeted and cellular therapies for relapsed/refractory mantle cell lymphoma: immunotherapeutic strategies and challenges.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  3. Article
  4. Review
  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

24 authors.

Hui WanDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Weicheng RenDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Mingyu YangDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden; Guangdong Provincial Key Laboratory of Human Disease Genomic, Shenzhen Key Laboratory of Genomics, BGI Research, Shenzhen, China.
Man NieDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, China.
Agata M WasikDivision of Pathology, Department of Laboratory Medicine, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
Likun DuDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Leire de Campos-MataDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Rui SunDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Zhiliang BaiDepartment of Biomedical Engineering, Yale University, New Haven, CT, USA.
Archibald EnninfulDepartment of Biomedical Engineering, Yale University, New Haven, CT, USA.
Yating WangDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Mattias BerglundDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Rose-Marie AminiDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Xiaobo LiGuangdong Provincial Key Laboratory of Human Disease Genomic, Shenzhen Key Laboratory of Genomics, BGI Research, Shenzhen, China.
Chunli YangDepartment of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China; Department of Medical Oncology, West China Hospital, Sichuan University, Chengdu, China.
Xiaofei YeKindstar Global Precision Medicine Institute, Wuhan, China.
Zhi-Zhang YangDivision of Hematology and Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Stephen M AnsellDivision of Hematology and Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Dongbing LiuGuangdong Provincial Key Laboratory of Human Disease Genomic, Shenzhen Key Laboratory of Genomics, BGI Research, Shenzhen, China; BGI Genomics, Shenzhen, China.
Mirjam van der BurgLaboratory for Pediatric Immunology, Department of Pediatrics, Willem Alexander Children's Hospital, Leiden University Medical Center, Leiden, the Netherlands.
Rong FanDepartment of Biomedical Engineering, Yale University, New Haven, CT, USA.
Kui WuGuangdong Provincial Key Laboratory of Human Disease Genomic, Shenzhen Key Laboratory of Genomics, BGI Research, Shenzhen, China; BGI Genomics, Shenzhen, China. Electronic address: wukui@genomics.cn.
Birgitta SanderDivision of Pathology, Department of Laboratory Medicine, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden. Electronic address: birgitta.sander@ki.se.
Qiang Pan-HammarströmDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden. Electronic address: qiang.pan-hammarstrom@ki.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mantle cell lymphoma (MCL) is a rare but often aggressive type of B cell lymphoma with a high risk of relapse. To explore intratumoral clonal diversity and tumor evolution related to disease relapse, we integrate single-cell RNA and B cell receptor sequencing with whole-genome sequencing in 20 diagnosed/untreated and/or relapsed samples from 11 MCL patients. Our results reveal significant intratumor heterogeneity in MCL already at diagnosis. We further show that the evolutionary paths during disease progression for each patient are unique, where minor clones present at diagnosis may acquire different mutations and copy-number variations and/or migrate to various microenvironments. Despite significant interpatient heterogeneity, recurrent genetic and transcriptomic changes in tumor cells affecting key signaling pathways, along with alterations involved in the tumor microenvironment, are also observed during disease progression. Taken together, our findings elucidate the diverse and dynamic tumor-immune evolution processes associated with disease progression and relapse in MCL.

Indexed as

Lymphoma, Mantle-CellNeoplasm Recurrence, LocalTumor MicroenvironmentAgedClonal EvolutionDisease ProgressionDNA Copy Number VariationsFemaleHumansMaleMiddle AgedMutationReceptors, Antigen, B-CellRecurrenceTranscriptomeReceptors, Antigen, B-Cellclonal evolutionimmunotherapymantle cell lymphomarelapsescRNA-seqsingle-cell RNA sequencingtumor heterogeneitytumor microenvironment

Identifiers

PMID40876452
PMCPMC12490240

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Registered trials

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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.